GYENNO帕金森宣传片配音稿
医疗之旅
轻音乐报时滴滴声总版头节目版头HELLOHELLO亲爱的听众朋友们大家中午好，欢迎收听FM760流溪之声中午档节目到点就游！我是主持人豆豆。
我是小鱼~音乐豆豆：上一期呢豆豆一个人很厉害的带大家把中国很有代表性的古镇游了个遍。
小鱼：。
小鱼由于喉咙痛就没有和大家一起。
（发挥）所以说健康很重要豆豆：是啊。
要问当前最热的话题是什么？“抢盐”、“核污染”、“瘦肉精”等等热点关注无疑将话题锁定在“健康”。
在度假的同时强身美体已经成为新的旅游动机，是当今旅游主题的时尚重点。
小鱼：当旅游成为一种时尚，就不再是走马观花，旅游同样可以引领一个时代的潮流。
豆豆：很反对那种走马观花的旅游方式。
那不是旅游是花钱找罪受小鱼：没错，。
豆豆：核污染就是浮云，保养健康才是王道。
让我们一起来进行今天的旅程----医疗旅行！音乐医疗旅行近年在中国突然升温。
2010年韩国的医疗观光推荐团出现在各地的旅游展会上。
日本也正加快医疗旅游的推广。
一时间国内旅行社、国际旅游中介、医疗公司等也都闻风而动。
医疗旅行最原本的概念是医院、疗养、保健、度假四者结合起来，主要指人们定居地的医疗服务太昂贵或不完善到外地寻求较相宜的保健服务并与休闲旅游相结合发展而成的一种新产业。
如今，随着中国人出境游渐趋常态，很多人也开始考虑去境外做一次医疗之旅。
境外医疗旅行的开销究竟有多大？治疗环境如何？随我一同对中国周边医疗旅游熟地展开一下调查，也为各地区医疗旅游成本算一笔账，看看这些国家医疗旅游的门槛有多高吧？韩国整形，吃顿饭的功夫。
亲历评价：报价与实际开销差别大，医疗服务不错，但整个旅程中观光内容太少韩国人喜欢整容天下人都知道，六七成的韩国女性一生中都做过一次以上整容手术。
甚至就连政界要人，也有热衷整容的。
韩国前总统卢武铉就曾经在就职期间整过容。
此类事情在其他国家较少有所听闻（个人是比较不喜欢韩国这个名族的。
在看韩国明星的MV 电影时，我要很努力很努力记得女主角A B C D…因为在我看来都长一个样子，太难认了）基于如此广泛的群众基础，韩国整容技术迅速成熟。
JBL SoundBoost 说明书
SOUNDBOOST SPEAKERAttach your Moto Mods™Align the camera lens on the back of your phone with the speaker, and then align the sides and bottom of the phone with the speaker until they snap together.Note: Make sure the connectors are clean and dry. Also, remove your phone case if you use one.Caution: Before using your device, please read the safety, regulatory, and legal information at the back of this guide.Compatibility Requirements:Moto Z Phone with Moto Mods Platform 1.0or laterQuick setupWhen you attach the speaker, your phone automatically guides you through setup. Follow the on-screen instructions to get started.Play mediaOnce your speaker is attached, begin using your phone as usual to play music or watch videos. Media will automatically play through the JBL SoundBoost speaker when attached to the phone. Adjust volumeTo change the volume for your speaker, use your phone’s volume controls.Charge itFully charge before using your speaker.Tip: If your phone is still attached to the speaker,charging the phone is the best way to charge both at the same time.Charging status lights Charging port Charge levelbutton slow blinking green ChargingFull chargePartially charged:51-99%16-50%6-15%Very low power steady green, then off steady amber, then off steady red, then off rapid blinking redrapid blinking green, or steady green when chargingTips & TricksLooking for more?•Camera: You can still use your phone’s camera when the speaker is attached.•Connection vibration: When you successfully attach your Moto Mod to your phone, you feela slight vibration.IMPORTANT SAFETY INSTRUCTIONSFor all products:1.Read these instructions.2.Heed all warnings.3.Follow all instructions.4.Do not install this apparatus near any heatsources such as radiators, heat registers, stoves or other apparatus (including amplifiers) thatproduce heat.e only attachments/accessories specified bythe manufacturer.6.Do not expose batteries to excessive heat suchas sunshine, fire or the like.CAUTION FCC AND IC STATEMENT FOR USERS (USA AND CANADA ONL Y)This device complies with part 15 of the FCC Rules. Operation is subject to the following two conditions: (1)This device may not cause harmful interference, and(2)this device must accept any interference received,including interference that may cause undesired operation.CAN ICES-3(B)/NMB-3(B)Federal Communication Commission Interference StatementThis equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to Part15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions,may cause harmful interference to radio communica-tions. However,there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures:•Reorient or relocate the receiving antenna.•Increase the separation between the equipment and receiver.•Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.•Consult the dealer or an experienced radio/TV technician for help.Caution: Changes or modifications not expressly approved by HARMAN could void the user’s authority to operate the equipment.WEEE NoticeThe Directive on Waste Electrical and Electronic Equipment (WEEE), which entered into force as European law on14February 2014, resulted in a major change in the treatment of electrical equipment at end-of-life.The purpose of this Directive is,as a first priority,the prevention of WEEE, and in addition, to promote the reuse,recycling and other forms of recovery of such wastes so as to reduce disposal. The WEEE logo on the product or on its box indicating collection for electrical and electronic equipment consists of the crossed-out wheeled bin, as shown below.This product must not be disposed of ordumped with your other household waste.You are liable to dispose of all yourelectronic or electrical waste equipment byrelocating over to the specified collection point for recycling of such hazardous waste. Isolated collection and proper recovery of your electronic and electrical waste equipment at the time of disposal will allow us to help conserving natural resources.Moreover,proper recycling of the electronic and electrical waste equipment will ensure safety of human health and environment. For more information about electronic and electrical waste equipment disposal, recovery, and collection points, please contact your local city center, household waste disposal service, shop from where you purchased the equipment, or manufacturer of the equipment.RoHS ComplianceThis product is in compliance with Directive2011/65/EU of the European Parliament and of the Council of 8 June2011 on the restriction of the use of certain hazardous substances in electrical and electronic equipment.For Products That Include BatteriesEU Batteries Directive 2013/56/EUA new battery directive 2013/56/EU on Battery and Accumulator replacing directive entered into force on the 1 July 2015.The directive applies to all types of batteries and accumulators(AA, AAA, button cells, lead acid, rechargeable packs) including those incorporated into appliances except for military, medical and power tool applications.The directive sets out rules for collection,treatment, recycling and disposal of batteries, and aims to prohibit certain hazardous substances and to improve environmental performance of batteries and all operators in the supply chain.Instructions for Users on Removal,Recycling and Disposal of Used BatteriesT o remove the batteries from your equipment or remote control,reverse the procedure described in the owner’s manual for inserting batteries.For products with a built-in battery that lasts for the lifetime of the product, removal may not be possible for the user.In this case,recycling or recovery centers handle the dismantling of the product and the removal of the battery.If,for any reason,it becomes necessary to replace such a battery, this procedure must be performed by authorized service centers.In the European Union and other locations, it is illegal to dispose of any battery with household trash. All batteries must be disposed of in an environmentally sound manner.Contact your local waste-management officials for information regarding the environmentally sound collection, recycling and disposal of used batteries. WARNING:Danger of explosion if battery is incorrectly replaced.T o reduce risk of fire or burns, don’t disassemble,crush,puncture, short external contacts,expose to temperature above60°C (140°F), or dispose of in fire or water.Replace only with specified batteries.The symbol indicating‘separate collection’for all batteries and accumula-tors shall be the crossed-out wheeled bin shown below:In case of batteries,accumulators and button cells containing more than0.0005 % mercury,more than 0.002 % cadmium or more than0.004 % lead, shall be marked with the chemical symbol for the metal concerned: Hg, Cd or Pb respectively. Please Refer to the below symbol:For All Products Except Those with Wireless Operation:HARMAN International hereby declares that this equipment is in compliance with the EMC2014/30/EU Directive,LVD2014/35/EU Directive and RoHS 2011/65/EU Directive.The declaration of conformity may be consulted in the support section of our Web site,accessible from.SET UP INFORMATION & PRODUCT REGISTRA-TIONCongratulations with the purchase of your new Product. We have done our utmost to make your experience the best one possible.If you have any questions when setting up your Product and would like some helpful hints, we recommend that you visit the relevant country specific support website for your Product: . There you will also find relevant contact information. If you cannot find the information you are looking for,please contact the vendor that sold the Product to you or contact the relevant JBL customer support center by electronic mail or phone.We recommend that you register your Product via the relevant country specific website for your Product. Your registration will allow us to inform you about updates for certain products, possible new offers and new Products and/or applications. Registering is easy;just follow the instructions on the relevant country specific website for your Product.NOTE: THIS LIMITED WARRANTY DOES NOT APPL Y TO CONSUMERS IN THE EUROPEAN ECONOMIC AREA (EEA) MEMBER STATES AND THE RUSSIAN FEDERATION AS THEY ARE PROTECTED BY LOCAL CONSUMER LAW AND BENEFIT FROM LOCAL STATUTORY WARRANTIESLIMITED WARRANTYWHO IS PROTECTED BY THE WARRANTYThis limited warranty (the “Limited Warranty”) protects only the original end-user (“you” or“your”), and is not transferable and is applicable only in the country (excluding EEA member states and the Russian Federation) in which you originally purchased your JBL Product (the “Product”). Any attempt to transfer this warranty shall immediately make this warranty void.LIMITED WARRANTYHARMAN International Industries, Incorporated (“HARMAN”) is the manufacturer and through its local subsidiary,warrants to you that the Product (including components provided in/with the Product) will be free from defects in workmanship and materials for a period of ONE year from the date of retail purchase by you(the“Warranty Period”). During the Warranty Period, the Product (including components),will be repaired or replaced at HARMAN’s option, without charge for either parts or labor OR at HARMAN’s sole option, the price of the Product may be refunded, subject todepreciation based on your purchase price for the Product pro-rated over the remaining balance of the Warranty Period.Any warranty service or replacement of parts will not extend the Warranty Period.This Limited Warranty does not cover defects which are a result of: (1) damage caused by accident, unreasonable use or neglect (including the lack of reasonable and necessary maintenance);(2) damage during shipment (claims must be presented to the carrier); (3) damage to, or deterioration of, any accessory or decorative surface;(4)damage resulting from failure to follow instructions contained in your owner’s manual; (5) damage resulting from the performance of repairs by someone other than an authorized JBL service center;(6)deterioration of component parts, the nature of which is to become worn or depleted with use,such as batteries and headphone ear pads. Furthermore, this Limited Warranty covers only actual defects within the Product itself, and doesnot cover the cost of installation or removal from a fixed installation, setup or adjustments, claims based on misrepresentation by the seller, performance variations resulting from installa-tion-related circumstances such as source quality or AC power or Product modifications, any unit on which the serial number has been effaced, modified or removed, or units used for other than home use. This Limited Warranty is valid only for JBL products purchased from an authorized dealer.Except to the extent expressly prohibited in your jurisdiction by applicable law,all implied warranties, including fitness for a particular purpose and merchantability are hereby excluded and in no event shall HARMAN or any HARMAN subsidiary be liable for any indirect, direct, incidental, special or consequential loss or damages whatsoever(including, without limitation, other pecuniary loss) arising out of the use of or inability to use the Product, even if HARMAN and/or a HARMAN subsidiary have been advised of the possibility of such damages. T o any extent that HARMAN cannot lawfully disclaim implied warranties under this Limited Warranty, all such implied warranties are limited in duration to the duration of this warranty. Some jurisdictions do not allow the exclusion or limitation of incidental or consequential damages or exclusions or limitations on the duration of implied warranties or conditions, so the above limitations or exclusions may not apply to you. This warranty gives you specific legal rights, and you may also have other rights that vary by jurisdiction.HOW TO OBTAIN WARRANTY SERVICEContact the dealer who sold you this Product, or contact JBL customer support using the contact information on the relevant country specific support website for your Product to request warranty service.T o validate your right to this Limited Warranty,you must provide the original sales invoice or other proof of ownership and date of purchase.Do not return your Product without prior authorization from the corresponding dealer or HARMAN. Warranty repair of the HARMAN Product must be carried out by an authorized dealer or service center. Unauthorized warranty repair will void the warranty and is performed at your sole risk. You are also welcome to consult the relevant country specific HARMAN support website for your Product for helpful hints.WHO PAYS FOR WHATThis Limited Warranty covers all expenses for labor and materials required for the repair OR replace-ment of the Product that is found to be defective, and a reasonable return shipping charge within the country of repair. Please be sure to save the original shipping carton(s), because a charge will be madefor additional cartons/packaging.You will be charged for the cost of examining a unit that is not in need of repair (including resulting shipping costs), or for necessary repairs not covered by this Limited Warranty.We sincerely thank you for your expression of confidence in JBL.We wish you many years of listening pleasure.Open source information:This Moto Mod accessory is intended to be interfaced with a Motorola mobile device and may include Open Source Software (the “Software”) copyrighted and distributed under an MITlicense and BSD-style licenses, including a modified BSD license, a BSD-like license and acompatible BSD license.The Software is distributed WITHOUT ANY WARRANTY; without even the implied warranty of MERCHANTABILITY or FITNESS FOR A PARTICU-LAR PURPOSE.T o view the text of the licenses, acknowledgments, required copyright notices and fulldisclaimer provisions for the Software used on this Moto Mod, please go to APPS > Settings >Moto Mods > Legal Information > Open source licenses on the Motorola mobile device after itis connected to this Moto Mod.Manufactured, distributed and sold by Harman International a Moto Mod™ licensee, who has certified that this product meets the applicable Moto Mod performance standards. Motorola Mobility LLC and Motorola Trademark HoldingsLLC are not responsible for the operation of this product or its compliance with safety and regulatory standards.MOTOROLA, the Stylized M Logo, MOTO and the MOTO family of marks are trademarks of Motorola Trademark Holdings, LLC.All other trademarks are the property of their respective owners. © 2016 Motorola Mobility LLCTR02778_B。
最新帕金森-双侧STN-DBS电极植入术+刺激器植入术护理教学讲义PPT
❖ 优点：手术时间短、创伤小、并发症少 ❖ 缺点：仅改善肢体症状、费用昂贵
帕金森病（Parkinson disease，PD）
手术方法
第一步：MR扫描进行靶点定位
第二步：入手术室局麻，穿刺定位，植入 脑深部电极
第三步：根据体外临时刺激器刺激判断疗 效及副反应，确定靶点
第四步：改行气管内麻醉，将脉冲器植入 右侧锁骨下胸部皮下，延伸导线经颈 部皮下达耳后与皮下刺激电极连接
帕金森病（Parkinson disease，PD）
手术适应症
1.典型PD 2.曾对左旋多巴制剂有效 3.经系统药物治疗后症状再无法控制或出现运动障
碍合并症 4.调整药物亦无法改善 5.没有严重的认知和精神障碍及严重脑萎缩 6.确诊后经过左旋多巴治疗治疗至少5年
帕金森病（Parkinson disease，PD）
帕金森病（Parkinson disease，PD）
❖ 出院指导
❖ （1）嘱患者配合进行规律的术后程控和随访，术后1月 回院调整参数。
❖ （2）远离高热环境，如桑拿房；远离磁场环境，如冰箱、 音响、微波炉等；禁止进行磁共振检查。外出活动时随 身携带植入识别卡以便在需要时获得帮助。
❖ （3）电池寿命一般可使用5~10年，如果电池耗尽可通过 外科手术更换脉冲器。
帕金森-双侧STN-DBS电极植 入术+刺激器植入术护理
帕金森病（Parkinson disease，PD）
流行病学
中国 发病率：44.3/10万人口 患者：34.8/10万人口
LOGO
帕金森病（Parkinson disease，PD）
概述
❖ 一种常见于中老年的中枢神经系统疾病 ❖ 多在60岁以后发病 ❖ 疾病呈进行性发展 ❖ 病因仍然不明，由于脑部炎症、药物中毒、血管
御稀灵虫草口服液电台专题广播稿 - 猪八戒网.
御稀灵虫草口服液电台专题广播稿收音机前亲爱的听众朋友大家好：（语气加重加长）首先非常感谢听众朋友在百忙之中抽出时间来收听本台的健康知识讲座。
今天由我来主持，为大家讲讲关于健康养生中不可多得的保健养生口服液——御稀灵虫草口服液。
下面我就跟您谈谈御稀灵虫草口服液的相关内容。
要了解御稀灵虫草口服液，首先要知道冬虫夏草是什么？它究竟是怎么长成的，它到底是条虫呢？还是一棵不起眼的草？自古以来，一般人对于冬虫夏草都感到神秘莫测，同时它也确实充满神奇色彩，早在1757年《本草从新》中就有“冬虫夏草甘平保肺，益肾，补精髓，止血化痰，治膈症皆良”的记载。
冬虫夏草顾各思义——冬天是条虫，夏天长成了草。
冬虫夏草又称夏草冬虫、冬虫草、虫草。
冬虫夏草是我国传统的名贵中药，与人参、鹿茸齐名，并列为三大补品。
它主要分布在四川、云南、贵州、甘肃、青海、西藏等海拔3000～4000m高山草甸土层中。
其中以青海西藏冬虫夏草产量最大。
关于虫草，前人也曾有诗说：“冬虫夏草名符实，变化生成一气通。
一物竟能兼动植，世间物理信难穷。
”冬虫夏草始载于《本草从新》。
说：“四川嘉定府所产者最佳。
云南、贵州所出者次之。
冬在土中，身活如老蚕，有毛能动，至夏则毛出土上，连身俱化为草。
若不取，至冬则复化为虫。
”《本草纲目拾遗》对其记载更加详细：“夏草冬虫，出四川江油县化林坪，夏为草，冬为虫，长三寸许，下跌六足，绝类蚕，羌俗采为上药。
”并引《七椿园西域闻见录》中说：“夏草冬虫生雪山中，夏则叶歧出类韭．根如朽木，凌冬叶干，则根蠕动化为虫。
”又引《柳崖外编》中说：“冬虫夏草，一物也。
冬则为虫，夏则为草，虫形似蚕，色微黄，草形似韭，叶较细。
”综合上述文献对其形态的描述和产地、生长环境的记述，并参照《植物名实图考》的附图，可以确定，麦角菌科虫草属真菌冬虫夏草菌及其寄生的复合体是传统的药用冬虫夏草。
然《本草纲目拾遗》又有记载，书中说：“《四川通志》中说：冬虫夏草出里塘拨浪工山，性温暖，补精益髓。
诺尔康人工耳蜗康复指南说明书
诺尔康官方公众号聆听，让生活更美好Hear more,live better在康复的过程中，经常会有家长来咨询，问得最多的问题就是为什么已经植入了人工耳蜗还需要做康复、为什么我家孩子2岁了还不会叫爸爸妈妈、为什么我的孩子融入不了同龄儿童、在家可以做的一些康复活动有哪些、能听到声音但是听不懂声音是怎么回事��针对以上的家长和用户的康复困惑点，本手册做出系统的解答，希望在您孩子或您的人工耳蜗康复道路上提供支持。
1、为什么要尽早接受人工耳蜗植入2、听力损失对语言发展的影响3、听力损失对言语发展的影响4、听力损失对认知发展的影响5、为什么植入人工耳蜗需要建立适当的期望值6、如何构造良好的听觉环境7、家庭康复的重要性8、多久才能康复好9、赞美、表扬的作用10、如何选择康复机构11、喜欢看口型怎么办12、植入人工耳蜗需满足哪些要求13、对双侧人工耳蜗用户来说，怎样避免两侧听力不平衡带来的烦恼DIRECTORY目录概述P R E F A C E前言020203030304040405050606061、佩戴了助听设备就能说得清楚吗2、开机两个月，还不怎么会发音，一般开机多久会有意义的发音呢3、听得挺好的，就是发音不清楚4、“爸爸”说成“大大”怎么办5、听的很好，但就是不开口说话6、韵母相近的音节容易读错7、发音不清楚的误区8、发音时而清楚时而不清楚是怎么回事9、学习说话的时候，家人如何引导10、发音的时候太着急了要怎么办11、有口型没声音如何解决呢12、单个字说的还好，在长句子中就听不清13、不开口说话，越让说就越不说，平时放松状态下发音还多一些，这是什么原因呢14、说话“口吃”怎么办15、怎么发鼻韵母？比如说ing 或ong 16、如何练习声调，提高标准度17、鼻音功能亢进18、呼吸训练的重要性发音篇成人篇080808080909091010101010111111111212141414151515161616161717181818181、为什么成人佩戴了助听设备还需要做听觉训练2、老年人戴上了助听设备还是有很多内容听不清楚3、60多岁的大伯性格急躁不愿意佩戴人工耳蜗如何处理4、成人可以在家做的一些听觉活动5、七十多岁的大伯说戴上耳蜗有太多“噪音”6、老年人植入耳蜗后也需要做康复训练吗7、开机快一年了，还是听不清，还有进步空间吗8、已经21岁了，语前聋，没有上过语训课，简单的交流能听懂，说话不标准，还有康复的希望吗9、开机两个月了，还是不能识别言语声10、影响成人康复的因素有哪些11、聆听技巧有哪些呢12、听声习惯、说话习惯的问题13、如何在嘈杂声中聆听14、人工耳蜗开机后，为什么“听不好”15、开机以后多久可以接打电话16、工作环境噪音很大，吵的都不想戴，这样戴耳蜗影响康复吗儿童篇其它20 20 21 21 21 21 22 22 22 22 22 23 23 23 24 24 24262626272728282829292930303030313131311、耳蜗开机后为什么会有沙沙沙的声音，需要适应多久才能听清楚电话和电视里的声音2、佩戴人工耳蜗以后有什么注意事项3、人工耳蜗和助听器有什么区别4、人工耳蜗可以解决耳鸣吗5、可以一侧佩戴助听器，另一侧植入人工耳蜗吗6、人工耳蜗多久干燥一次7、有没有好的软件可以推荐学习呢8、听力损失后为什么要加强运动9、林氏六音的重要性10、可以跟着电视学习语言吗11、在家里应该如何做一些语言训练呢12、开机与调试13、植入人工耳蜗后能做磁共振吗14、电磁炉，美容仪，烫发对人工耳蜗有影响吗15、植入人工耳蜗后能游泳吗？耳朵里进水会不会影响植入体16、冬季如何预防静电17、出汗后如何保养体外机18、晚上睡觉的时候是否可以戴体外机19、植入人工耳蜗后是否可以进行放疗或者做高压氧1、影响聋儿康复的因素2、18个月左右的宝宝是否适合去康复中心做训练3、父母要如何帮助孩子选择玩具，不同的年龄层孩子适合怎样的玩具4、对于刚刚开机能听到声音的孩子，为什么叫他却没有反应5、单侧聋的儿童不愿意佩戴助听设备怎么办6、如何培养孩子的社交能力7、为什么我家孩子不会和同龄儿童一起游戏8、如何提升孩子的专注力9、小朋友在家可以做的一些听觉活动10、为什么我家的孩子总是发脾气11、孩子喜欢扔东西，怎么办12、注意力训练的小游戏13、怎么利用周围资源进行教学呢？14、孩子太喜欢玩手机，可以完全禁止吗15、怎么将学习与生活联系起来16、孩子已从康复学校毕业，去幼儿园和小学应该如何适应17、孩子上一年级了，听的还可以，就是注意力不集中01概述SUMMARY听觉语言发育出生后就开始，直到两岁左右发育成熟。
厦门市博爱康复中心专题片《博爱,点亮希望》脚本
博爱康复中心，响应时代的召唤，满腔热诚为厦门市残疾人群体服务，给他们点亮一盏盏希望的灯火。
35秒
片头
康复中心外景，大门
医保(IC卡)定点单位
工伤康复协议单位
厦门市博爱康复中心，成立于2001年，是经市编委批准、市残联直接领导的事业单位，被厦门市卫生局审批为二级乙等非营利性康复专科机构，是厦门市医保定点单位、工伤康复协议单位。下设三个实体：市特需儿童援助中心，市残联康复医院，市残疾人辅具适配中心，
2009年厦门博爱康复中心经过综合评估被中国残联的长江新里程项目办公室选拔为“脑瘫引导式教育”定点康复机构，参与的脑瘫儿童康复与残疾预防项目，在2009-2011年完成50名脑瘫孩子的任务。
截止2010年12月，中心已完成了二期引导式教育。共完成25例，已有13名孩子进入正常幼儿园就读，该项目得到家长高度认可和欢迎。
设有运动治疗科、物理治疗科、作业治疗科、中医传统治疗科、语训治疗科和视力康复科等科室，可为脑瘫、偏瘫、截瘫、视力残疾患者截肢和老年慢性疾病患者提供康复治疗服务。
康复医院引进美国STORZ公司超声乳化仪、德国蔡司眼科手术显微镜、眼科A\B超、角膜曲率计等。主要开展白内障超声乳化人工晶体植入术，承担厦门市政府白内障复明的主要工作；低视力康复；弱视康复训练和验光配镜；眼底病等。目前已成功完成白内障超声乳化手术3000余例。
30秒
特需儿童援助中心招牌，环境，设备，器具。大课，单训，亲子个训教学情境。
字幕：
截止2010年上半年，中心共康复各类残疾儿童422名已有196名儿童进入正常幼儿园和普通小学就读。
特需儿童援助中心前身是创办于2003年的厦门博爱康复中心残疾儿童康复教育部。
抖音仙鹤大叔医疗科普合集
抖音仙鹤大叔医疗科普合集公司内部档案编码：[OPPTR-OPPT28-OPPTL98-OPPNN08]鹤叔医疗科普合集（）灯火阑珊整（）西伯利亚狼二次美化整理整理者按：2019年10月份，一个偶然的机会通过抖音关注了鹤叔，他教我们通过最简单的方式，使用最便宜、易得的药物来解决常见的皮肤问题。
不仅告诉我们治疗的方法，还解析了疾病的发病原理，使我们解除了痛苦，甚至治愈了很多久拖不愈的疑难杂症。
鹤叔说他做科普一不为名，二不图利，就是希望老百姓多些知识的储备，少些后悔。
通过鹤叔的科普，越来越多的人自己在家就解决了原本四处求医都不见好转的皮肤问题。
杏林春满，医者仁心。
鹤叔的科普如星星之火，以燎原之势在造福更多的百姓。
希望我的整理稿，如一阵清风，带着这星火传递给更多有缘人。
感恩鹤叔的无私科普，感谢鹤粉-壮壮的校对和查漏补缺！第一篇：抖音短视频科普集锦()1、鹤叔讲课一不为名，二不图利，希望老百姓少后悔：80多岁老人得带状疱疹听人说激素有危害，不用，过了治疗期疼得拿头撞墙，生不如死；十几岁的小孩激光治了跖疣不懂预防感染，差点截肢；漂亮女孩乱用化妆品，过敏后乱抹激素闹成激素依赖性皮炎。
这类事触目惊心，就因为老百姓脑子里头没有这些知识储备。
2、面部湿疹：夏天抱孩子不得当，宝宝的口水和大人的汗水混合会对宝宝的细嫩皮肤造成伤害，大人皮肤上的细菌也趁机入侵孩子的面部，接触部位不通风，刺激和细菌很容易造成面部湿疹。
解决方法：在大人的肩膀放一块干净的手巾，孩子的脸贴在手巾上，既通风又吸收汗液和口水，避免细菌入侵。
3、小儿湿疹：具备三只眼，第一只眼准确看清小孩体内毒素的眼，为什么皮肤不停出皮疹，本质是体内的毒素，其实就是一种神经介质，如果你不知道它的量就不知道用药到什么程度可以把它中和掉，不去根，所以病就要反复发；第二只眼看清皮疹的深度，深的用药强一些，浅的用药浅一些，因为外用药有副作用；第三只眼看清孩子生活中的哪些危险因素，及时避开，及时用药。
TS36.101v1.0.0
3GPP TS 36.101v1.0.0(2007-12)Technical Specification3rd Generation Partnership Project;Technical Specification Group Radio Access Network;Evolved Universal Terrestrial Radio Access (E-UTRA);User Equipment (UE) radio transmission and reception;(Release 8)The present docu ment has been developed within the 3r d Generation Partnership Project (3GPP TM) and may be further elaborated for the purposes of 3G PP. The present d ocument has not been subject to any approval process by the 3G PP Organizational Partners and shall not be implemented.This Specification is provided for fu ture development work within 3GPP only. The Organizational Partners accept no liability for any use of this Specification. Specifications and reports for implementation of the 3GPP TM system should be obtained via the 3GPP Organizational Partners' Publications Offices.KeywordsEUTRA, User Equipment (UE), radio, RF requirements3GPPPostal address3GPP support office address650 Route des Lucioles - Sophia AntipolisValbonne - FRANCETel.: +33 4 92 94 42 00 Fax: +33 4 93 65 47 16InternetCopyright NotificationNo part may be reproduced except as authorized by written permission. The copyright and the foregoing restriction extend to reproduction in all media.© 2006, 3GPP Organizational Partners (ARIB, ATIS, CCSA, ETSI, TTA, TTC).All rights reserved.ContentsForeword (6)1Scope (7)2References (8)3Definitions, symbols and abbreviations (9)3.1Definitions (9)3.2Symbols (9)3.3Abbreviations (10)4General (11)4.1Relationship between Minimum Requirements and Test Requirements (11)5Frequency bands and channel arrangement (12)5.1General (12)5.2Frequency bands (12)5.3TX–RX frequency separation (12)5.4Channel arrangement (12)5.4.1Channel spacing (12)5.4.2Channel bandwidth (13)5.4.2.1 Nominal channel bandwidth (13)5.4.2.2Additional channel bandwidth (14)5.4.3Channel raster (15)5.4.4Channel number (15)5.4.5EA RFCN (16)6Transmitter characteristics (17)6.1General (17)6.2Transmit power (17)6.2.1Maximum Output Power (MOP) (17)6.2.2UE Power class (17)6.2.3Maximum Power Reduction (MPR) (18)6.2.4Additional Maximum Power Reduction (A-MPR) (18)6.3Output power dynamics (19)6.3.1Power control (19)6.3.2Minimum output power (19)6.3.3Transmit ON/OFF power (20)6.4Control and monitoring functions (20)6.4.1Out-of-synchronization handling of output power (20)6.5Transmit signal quality (20)6.5.1Frequency Error (20)6.5.2Transmit modulation (20)6.5.2.1Error Vector Magnitude (20)6.5.2.1.1Minimum requirement (20)6.5.2.2IQ-component (21)6.5.2.2.1Minimum requirements (21)6.5.2.3In-band emissions (21)6.5.2.3.1Minimum requirements (21)6.6Output RF spectrum emissions (21)6.6.1Occupied bandwidth (22)6.6.2Out of band emission (22)6.6.2.1Spectrum emission mask (22)6.6.2.1.1Minimum requirement (22)6.6.2.2Additional Spectrum Emission Mask (23)6.6.2.2.1Minimum requirement (network signalled value “NS_03”) (23)6.6.2.2.2Minimum requirement (network signalled value “NS_04”) (23)6.6.2.2.3Minimum requirement (network signalled) (24)6.6.2.3Adjacent Channel Leakage Ratio (24)6.6.2.3.1Minimum requirement E-UTRA (24)6.6.2.3.2Minimum requirements UTRA (25)6.6.2.4Additional ACLR require ments (25)6.6.2.4.1Minimum requirements (network signalled value “NS_02”) (25)6.6.3Spurious emissions (26)6.6.3.1Minimum requirements (26)6.6.3.2Spurious emission band UE co-existence (26)6.6.3.3Additional spurious emissions (27)6.6.3.3.1Minimum requirement (network signalled value “NS_05”) (27)6.6.3.3.2Minimum requirements (network signalled) (27)6.7Transmit intermodulation (27)7Receiver characteristics (29)7.1General (29)7.2Diversity characteristics (29)7.3Reference sensitivity power level (29)7.3.1Minimum requirements (QPSK) (29)7.3.2Maximum Sensitivity Reduction (MSR) (30)7.4Maximum input level (30)7.4.1Minimum requirements (31)7.5Adjacent Channel Selectivity (A CS) (31)7.5.1Minimum requirements (31)7.6Blocking characteristics (32)7.6.1In-band blocking (32)7.6.1.1Minimum requirements (32)7.6.2Out of-band blocking (33)7.6.2.1Minimu m requirements (33)7.6.3Narrow band blocking (34)7.6.3.1Minimum requirements (34)7.7Spurious response (35)7.7.1Minimum requirements (35)7.8Intermodulation characteristics (35)7.8.1Wide band Intermodulation (35)7.8.1.1Minimum requirements (35)7.8.2Narrow band Intermodulation (36)7.8.2.1Minimum requirements (36)7.9Spurious emissions (36)7.9.1Minimum requirements (36)8Performance requirement (37)8.1General (37)8.1.1Dual-antenna receiver capability (37)8.1.1.1Simultaneous unicast and MBMS operations (37)8.1.1.2Dual-antenna receiver capability in idle mode (37)Annex A (normative): Measurement channels (38)A.1General (38)A.2UL reference measurement channels (38)A.3DL reference measurement channels (38)Annex B (normative): Propagation conditions (39)B.1General (39)B.2Propagation channel s (39)B.2.1Static propagation condition (39)B.2.2Multi-path fading propagation conditions (39)B.2.2.1Delay profiles (39)B.2.2.2Doppler spectrum (40)B.2.2.3Multi-Antenna channel models (42)B.2.2.4Combinations of channel model parameters (46)Annex C (normative): Downlink Physical Channels (47)C.1General (47)C.2Set-up (47)C.3Connection (47)Annex D (normative): Characteristics of the interf ering signal (48)D.1General (48)D.2Interference signals (48)Annex E (normative): Environmental conditions (49)E.1General (49)E.2Environmental (49)E.2.1Temperature (49)E.2.2Voltage (49)E.2.3Vibration (50)Annex F (informative): Change history (51)ForewordThis Technical Specification (TS) has been produced by the 3rd Generation Partnership Project (3GPP).The contents of the present document are subject to continuing work within the TSG and may change following formal TSG approval. Should the TSG modify the contents of the present document, it will be re-released by the TSG with an identifying change of release date and an increase in version number as follows:Version x.y.zWhere:x the first digit:1 presented to TSG for information;2 presented to TSG for approval;3 or greater indicates TSG approved document under change control.y the second digit is incremented for all changes of substance, i.e. technical enhancements, corrections, updates, etc.z the third digit is incremented when editorial only changes have been incorporated in the document.1 ScopeThe present document establishes the User Equipment (UE) minimum RF characteristics of E-UTRA for both FDD and TDD modes2 ReferencesThe following documents contain provisions which, through reference in this text, constitute provisions of the present document.∙References are either specific (identified by date of publication, edition number, version number, etc.) or non-specific.∙For a specific reference, subsequent revisions do not apply.∙For a non-specific reference, the latest version applies. In the case of a reference to a 3GPP document (including a GSM document), a non-specific reference implicitly refers to the latest version of that document in the same Release as the present document.[1] 3GPP TR 21.905[2] ETSI ETR 273: "Electromagnetic compatibility and Radio spectrum Matters (ERM); Improvement ofradiated methods of measurement (using test sites) and evaluation of the corresponding measurementuncertainties; Part 1: Uncertainties in the measurement of mobile radio equipment characteristics; Sub-part 2: Examples and annexes".[3] Recommendation ITU-R SM.329-10, “Unwanted emissions in the spurious domain”[4] Recommendation ITU-R M.1225, “Guidelines for Evaluation of Radio Transmission Technologies forIMT-2000”, ITU-R, 1997.[5] 3GPP TR 25.943 V6.0.0 (2004-12), “Deployment aspects (Release 6)”.[6] 3GPP TR 25.913: “Requirements for Evolved UTRA and UTRAN”.[7] 3GPP TS 45.005 V7.8.0 (2006-11), “3rd Generation Partnership Project; Technical Specification GroupGSM/EDGE Radio Access Network; Radio transm ission and reception (Release 7)”.[8] R4-070752, “Proposal for LTE channel models”[9] 3GPP TR 25.943 V6.0.0 (2004-12), “Deployment aspects (Release 6)”.3 Definitions, symbols and abbreviations3.1 DefinitionsFor the purposes of the present document, the following terms and definitions apply.<defined term> : <definition>.For the purposes of the present document, the terms and definitions given in TR 21.905 [x] and the following apply. A term defined in the present document takes precedence over the definition of the same term, if any, in TR 21.905 [x].Channel edge: The lowest and highest frequency of the carrier, separated by the channel bandwidth.Channel bandwidth: The RF bandwidth supporting a single E-UTRA RF carrier with the transmission bandwidth configured in the uplink or downlink of a cell. The channel bandwidth is measured in MHz and is used as a reference for transmitter and receiver RF requirements.Maximum Output Power: The mean power level per carrier of UE measured at the antenna connector in a specified reference condition.Mean power: When applied to E-UTRA transmission this is the power measured in the operating system bandwidth of the carrier. The period of measurement shall be at least one subframe (1ms) for frame structure type 1 and one subframe (0.675ms) for frame structure type 2 excluding the guard interval, unless otherwise stated.Occupied bandwidth: The width of a frequency band such that, below the lower and above the upper frequency limits, the mean powers emitted are each equal to a specified percentage β/2 of the total mean power of a given emission.Output power: The mean power of one carrier of the UE, delivered to a load with resistance equal to the nominal load impedance of the transmitter.Reference bandwidth: The bandwidth in which an emission level is specified.Transmission bandwidth: Bandwidth of an instantaneous transmission from a UE or BS, measured in Resource Block units.Transmission bandwidth configuration: The highest transmission bandwidth allowed for uplink or downlink in a given channel bandwidth, measured in Resource Block units.3.2 SymbolsFor the purposes of the present document, the following symbols apply:BW Channel Channel bandwidthF FrequencyF Interferer (offset) Frequency offset of the interfererF Interferer Frequency of the interfererF C Frequency of the carrier centre frequencyF DL_low The lowest frequency of the downlink operating bandF DL_high The highest frequency of the downlink operating bandF UL_low The lowest frequency of the uplink operating bandF UL_high The highest frequency of the uplink operating bandN DL Downlink EARFCNN Offs-DL Offset used for calculating downlink EA RFCNN Offs-UL Offset used for calculating uplink EARFCNN RB Transmission bandwidth configuration, expressed in units of resource blocksN UL Uplink EA RFCNRav M inimum average throughput per RBP Interferer Modulated mean power of the interfererΔF OOB Δ Frequency of Out Of Band emission3.3 AbbreviationsFor the purposes of the present document, the abbreviations given in TR 21.905 [1] and the following apply. An abbreviation defined in the present document takes precedence over the definition of the same abbreviation, if any, in TR 21.905 [1].ACLR Adjacent Channel Leakage RatioACS Adjacent Channel SelectivityA-MPR Additional Maximum Power ReductionAWGN Additive White Gaussian NoiseBS Base StationCW Continuous WaveDL DownlinkEA RFCN E-UTRA Absolute Radio Frequency Channel NumberE-UTRA Evolved UMTS Terrestrial Radio AccessEUTRAN Evolved UMTS Terrestrial Radio Access NetworkEVM Error Vector MagnitudeFDD Frequency Division DuplexFRC Fixed Reference ChannelHD-FDD Half- Duplex FDDMCS Modulation and Coding SchemeMOP Maximum Output PowerMPR Maximum Power ReductionMSR Maximum Sensitivity ReductionOOB Out-of-bandPA Power A mplifierREFSENS Reference Sensitivity power levelSNR Signal-to-Noise RatioTDD Time Division DuplexUE User EquipmentUL UplinkUMTS Universal Mobile Telecommunications SystemUTRA UMTS Terrestrial Radio AccessUTRAN UMTS Terrestrial Radio Access NetworkOther abbreviations used in the present document are listed in 3GPP TR 21.905 [1].4 General4.1 Relationship between Minimum Requirements and TestRequirementsThe Minimum Requirements given in this specification make no allowance for measurement uncertainty. The test specification TS 36.xxx section y defines Test Tolerances. These Test Tolerances are individually calculated for each test. The Test Tolerances are used to relax the Minimum Requirements in this specification t o create Test Requirements.The measurement results returned by the Test System are compared - without any modification - against the Test Requirements as defined by the shared risk principle.The Shared Risk principle is defined in ITU-R M.1545 [3].5 Frequency bands and channel arrangement5.1 GeneralThe channel arrangements presented in this clause are based on the frequency bands and channel bandwidths defined in the present release of specifications.NOTE: Other frequency bands and channel bandwidths may be considered in future releases.5.2 Frequency bandsE-UTRA is designed to operate in the frequency bands defined in Table 5.2-1.Table 5.2-1 E-UTRA frequency bands5.3 TX–RX frequency separation5.4 Channel arrangement5.4.1 Channel spacingThe spacing between carriers will depend on the deployment scenario, the size of the frequency block available and the channel bandwidths. The nominal channel spacing between two adjacent E-UTRA carriers is defined as following:Nominal Channel spacing = (BW Channel(1) + BW Channel(2))/2where BW Channel(1) and BW Channel(2) are the channel bandwidths of the two respective E-UTRA carriers. The channel spacing can be adjusted to optimize performance in a particular deployment scenario5.4.2 Channel bandwidthRequirements in present document are specified for the channel bandwidths listed in Table 5.4-1.Table 5.4-1 Transmission bandwidth configuration N RB in E-UTRA channel bandwidthsFigure 5.4-1 shows the relation between the Channel bandwidth (BW Channel) and the Transmission bandwidth configuration (N RB). The channel edges are defined as the lowest and highest frequencies of the carrier separated by the channel bandwidth, i.e. at F C +/- BW Channel /2.Figure 5.4-1 Definition of Channel Bandwidth and Transmiss ion Bandwidth Configuration.5.4.2.1 Nominal channel bandwidthTable 5.4.2-1 specifies the nominal channel bandwidth which are supported for the E-UTRA bandTable 5.4.2-1: E-UTRA channel bandwidth5.4.2.2 Additional channel bandwidthThe following additional channel bandwidth can be supported if certain relaxations of the UE performance are allowed or UE functionality is limited. These relaxations and limitations are TBD.Table 5.4.4.2-1: Additional E-UTRA channel bandwidth5.4.3 Channel rasterThe channel raster is 100 kHz for all bands, which means that the carrier centre frequency must be an integer multiple of 100 kHz.5.4.4 Channel numberThe carrier frequency in the uplink and downlink is designated by the E-UTRA Absolute Radio Frequency Channel Number (EA RFCN). The carrier frequency in MHz for the downlink is given by the following equation, where F DL_low and N Offs-DL are given in table 5.4.4-1 and N DL is the downlink EA RFCN.F DL = F DL_low + 0.1(N DL– N Offs-DL)The carrier frequency in MHz for the uplink is given by the following equation where F UL_low and N Offs-UL are given in table 5.4.4-1 and N UL is the uplink EARFCN.F UL = F UL_low + 0.1(N UL– N Offs-UL)Table 5.4.4-1 E-UTRA channel numbers5.4.5 EARFCN6 Transmitter characteristics6.1 GeneralUnless otherwise stated, the transmitter characteristics are specified at the antenna connector of the UE with a single transmit antenna. For UE with integral antenna only, a reference antenna with a gain of 0 dBi is assumed.6.2 Transmit power6.2.1 Maximum Output Power (MOP)The Maximum Output Power (MOP) defined in Table 6.2.1-1 is the broadband transmit power of the UE, i.e. the power in the channel bandwidth (clause 5.2) for all transmit bandwidth configurations (resource blocks).Table 6.2.1-1: Maximum Output Power (MOP)6.2.2 UE Power classThe following UE Power Classes define the nominal maximum output power. The nominal power is defined as the broadband transmit power of the UE, i.e. the power in the channel bandwidth (clause 5.2) of the radio access mode. The period of measurement shall be at least one [timeslot/ frame/TTI].Table 6.2.2-1: UE Power ClassThe transmission bandwidth configuration (resource blocks) for the maximum output power specified in Table 6.2.2-1 is defined in Table 6.2.2-2 below for QPSK modulation.Table 6.2.2-2: UE Power Class / channel bandwidth / transmission configuration6.2.3 Maximum Power Reduction (MPR)For UE PowerClass 3, the allowed Maximum Power Reduction (MPR) for the nominal maximum output power in 6.2.2 due to higher order modulation and transmit bandwidth configuration (resource blocks) is specified in Table 6.2.3-1.Table 6.2.3-1: Maximum Power Reduction (MPR) for PC 36.2.4 Additional Maximum Power Reduction (A-MPR)Additional ACLR and spectrum emission requirements can be signalled by the network to indicate that the UE shall meet also additional requirements in a specific deployment scenario. To meet these additional requirements the concept of A-MPR is introduced.For UE Power Class 3 the specific requirements and identified sub-clauses are specified in table 6.2.4-1 along with the allowed A-MPR values that may be used to meet these requirements. The allowed A-MPR values specified below are in addition to the allowed MPR requirements specified in clause 6.2.3.Table 6.2.4-1: Additional Maximum Power Reduction (A-MPR) / Spectrum Emission requirements6.3 Output power dynamics6.3.1 Power control6.3.2 Minimum output powerThe minimum controlled output power of the UE is defined as the broadband transmit power of the UE, i.e. the power in the channel bandwidth (clause 5.2) for all transmit bandwidth configurations (resource blocks), when the power is set to a minimum value.6.3.2.1Minimum requirementThe minimum output power is defined as the mean power in one sub-frame (1ms). The minimum output power shall be less than [-30] dBm.6.3.3 Transmit ON/OFF power6.4 Control and monitoring functions6.4.1 Out-of-synchronization handling of output power6.5 Transmit signal quality6.5.1 Frequency ErrorThe UE modulated carrier frequency shall be accurate to within ±0.1 PPM observed over a period of one sub-frame(1ms) for generic frame structure type 1 and one sub-frame (0.675ms) for frame structure type 2 excluding the guard period (Cyclic prefix).6.5.2 Transmit modulationTransmit modulation defines the modulation quality for expected in-channel RF transmissions from the UE. This transmit modulation limit is specified in terms of; an Error Vector Magnitude (EVM) for the allocated resources blocks (RB), an I/Q component and an in-band emissions for the non-allocated RB.6.5.2.1 Error Vector MagnitudeThe Error Vector Magnitude is a measure of the difference between the reference waveform and the measured waveform. This difference is called the error vector. Before calculating the EVM the measured waveform is corrected by the sample timing offset and RF frequency offset. Then the IQ origin offset is removed from the measured waveform.The measured waveform is further modified by selecting the absolute phase and absolute amplitude of the Tx chain. The EVM result is defined after the front-end IDFT as the square root of the ratio of the mean error vector power to the mean reference power expressed as a %. The measurement interval is one [timeslot] except when the mean power between slots is expected to change whereupon the measure ment interval is reduced by [] μs at each end of the slot. The IQ origin offset shall be removed from the evaluated signal before calculating the EVM; however, the removed relative IQ origin offset power (relative carrier leakage power) also has to satisfy the applicable requirement.6.5.2.1.1 M inimum requirementThe RMS average of the basic EVM measurements for [10 consecutive sub-frames] for the different modulations schemes shall not exceed the values specified in Table 6.5.2.1.1-1 for the parameters defined in Table 6.5.2.1.1-2.Table 6.5.2.1.1-1: Minimum requirements for Error Vector MagnitudeTable 6.5.2.1.1-2: Parameters for Error Vector Magnitude6.5.2.2 IQ-componentThe IQ origin offset is the phase and amplitude of an additive sinusoid waveform that has the same frequency as the reference waveform carrier frequency.6.5.2.2.1 Minimum requirementsThe relative carrier leakage power (IQ origin offset power) shall not exceed the values specified in Table 6.5.2.2.1-1.Table 6.5.2.2.1-1: Minimum requirements for Relative Carrier Leakage Power6.5.2.3 In-band emissions6.5.2.3.1 M inimum requirements6.6 Output RF spectrum emissionsThe output UE transmitter spectrum consists of the three components; the emission within the occupied bandwidth (channel bandwidth), the Out Of Band (OOB) emissions and the far out spurious emission domain.Figure 6.6-1: Transmitter RF spectrum6.6.1 Occupied bandwidthOccupied bandwidth is defined as the bandwidth containing 99 % of the total integrated mean power of the transmitted spectrum on the assigned channel. The occupied bandwidth for all transmission bandwidth configurations (Resources Blocks) shall be less than the channel bandwidth specified in Table 6.6.1-1Table 6.6.1-1: Occupied channel bandwidth6.6.2 Out of band emissionThe Out of band emissions are unwanted emissions immediately outside the assigned channel bandwidth resulting from the modulation process and non-linearity in the transmitter but excluding spurious emissions. This out of band emission limit is specified in terms of a spectrum emission mask and an Adjacent Channel Leakage power Ratio.6.6.2.1 Spectrum emission maskThe spectrum emission mask of the UE applies to frequencies (Δf OOB) starting from the edge of the assigned E-UTRA channel bandwidth. For frequencies greater than (Δf OOB) as specified in Table 6.6.2.1.1-1 the spurious requirements in clause 6.6.3 are applicable.6.6.2.1.1 Minimum requirementThe power of any UE emission shall not exceed the levels specified in Table 6.6.2.1.1-1 for the specified channel bandwidth.Table 6.6.2.1.1-1: General E-UTRA spectrum emission maskNote: As a general rule, the resolution bandwidth of the measuring equipment should be equal to the measurement bandwidth. However, to improve measurement accuracy, sensitivity and efficiency, the resolution bandwidth may be smaller than the measurement bandwidth. When the resolution bandwidth is smalle r than the measurement bandwidth, the result should be integrated over the measurement bandwidth in order to obtain the equivalent noise bandwidth of the measurement bandwidth.6.6.2.2 Additional Spectrum Emission MaskThis requirement is specified in ter ms of an “additional spectrum emission” requirement.6.6.2.2.1 Minimum requirement (network signalled value “NS_03”)Additional spectrum emission requirements are signalled by the network to indicate that the UE shall meet an additional requirement for a specific deployment scenario as part of the cell handover/broadcast message.When “NS_03” is indicated in the cell, the power of any UE emission shall not exceed the levels specified in Table6.6.2.2-1.Table 6.6.2.2.1-1: Additional requirements (FCC Part 22)Note: As a general rule, the resolution bandwidth of the measuring equipment should be equal to the measurement bandwidth. However, to improve measurement accuracy, sensitivity and efficiency, the resolution bandwidth may be smaller than the measurement bandwidth. When the resolution bandwidth is smaller than the measurement bandwidth, the result should be integrated over the measurement bandwidth in order to obtain the equivalent noise bandwidth of the measurement bandwidth.6.6.2.2.2 Minimum requirement (network signalled value “NS_04”)Additional spectrum emission requirements are signalled by the network to indicate that the UE shall meet an additional requirement for a specific deployment scenario as part of the cell handover/broadcast message.When “NS_04” is indicated in the cell, the power of any UE emission shall not exceed the levels specified in Table6.6.2.2.2-1.Table 6.6.2.2.2-1: Additional requirements (FCC Part 27)Note: As a general rule, the resolution bandwidth of the measuring equipment should be equal to the measurement bandwidth. However, to improve measurement accuracy, sensitivity and efficiency, the resolution bandwidth may be smaller than the measurement bandwidth. When the resolution bandwidth is smaller than the measurement bandwidth, the result should be integrated over the measurement bandwidth in order to obtain the equiv alent noise bandwidth of the measurement bandwidth.6.6.2.2.3 Minimum requirement (network signalled)6.6.2.3 Adjacent Channel Leakage RatioAdjacent Channel Leakage power Ratio (A CLR) is the ratio of the] filtered mean power centred on the assigned channel frequency to the filtered mean power centred on an adjacent channel frequency. ACLR requirements are specified for two scenarios for an adjacent E -UTRA and /or UTRA channel as shown in Figure 6.6.2.3 -1.Figure 6.6.2.3-1: Adjacent Channel Leakage requirements6.6.2.3.1 Minimum requirement E-UTRAE-UTRA Adjacent Channel Leakage power Ratio (E-UTRA ACLR) is the ratio of the filtered mean power centred on the assigned channel frequency to the filtered mean power centred on an adjacent channel frequenc y. The E-UTRA on channel and adjacent channel power is measured with a [rectangular measurement bandwidth filter.]6.6.2.3.2 Minimum requirements UTRAUTRA Adjacent Channel Leakage power Ratio (UTRA ACLR) is the ratio of the filtered mean power centred on the assigned E-UTRA channel frequency to the filtered mean power centred on an adjacent(s) UTRA channel frequency. UTRA Adjacent Channel Leakage power Ratio is specified for both the first UTRA 5 MHz adjacent channel (UTRA ACLR1) and the 2nd UTRA 5MHz adjacent channel (UTRA ACLR2) .The UTRA channel is measured with a 3.84 MHz RRC bandwidth filter with roll-off factor α =0.22. The E-UTRA channel is measured with a [rectangular measurement bandwidth filter]Table 6.6.2.3.2-1: Additional requirements6.6.2.4 Additional ACLR requirementsThis requirement is specified in terms of an additional UTRA ACLR2 requirement.6.6.2.4.1 Minimum requirements (network signalled value “NS_02”)”NS_02” is signalled by the network to indicate that the UE shall meet this additional requirement for a specific deployment scenario as part of the cell handover/broadcast message.The Additional ACLR requirements is specified for the 2nd UTRA 5MHz adjacent channel (UTRA ACLR2) .The UTRA channel is measured with a 3.84 MHz RRC bandwidth filter with roll-off factor α =0.22. The E-UTRA channel is measured with a [rectangular measurement bandwidth filter.]。
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开讲啦倪鑫演讲稿格式参考：让儿童医院变成儿童乐园
开讲啦倪鑫演讲稿格式参考：让儿童医院变成儿童乐园谢讲啦倪鑫演讲稿格式参考：让儿童病院酿成儿童乐土各人孬，尔的名字鸣倪鑫，去自于南京儿童病院。
咱们讲人吃五谷纯粮没有会没有抱病，并且尤为是孩子。
孩子一旦抱病当前，咱们时常讲一句话，孩子的安康波及到的是千野万户的健康。
方才尔正在上面，尔听到咱们掌管人讲，说正在座的列位，谁若是说挨一喷嚏、流一鼻涕您来没有来病院，提到那么一个答习题。
这真际上呢，那个答习题尔有很深的一个感到。
真际上尔的业余是弄耳鼻喉的，正在2012年调到了南京儿童病院。
否能正在座的列位野少皆来过儿童病院，当孩子发热须要输液的时分，您会天天到病院来，看完医生谢完药，输完液归野，第两地要从头再看医生、再挂号、再谢药、再输液。
其时尔便说，为何要那样作呢？便不克不及一高谢三地五地，而后让病人去了输液便走？甚至正在野门心输没有便完了？为何地地要往病院跑呢？那很费事啊！而后咱们的大夫说，说倪院少，你没有是不断弄儿科没去的，你没有懂，儿科跟成人纷歧样，他的病情变迁太快，天天皆有否能变迁。
以是他每一次再去输液的时分，咱们必然要大夫看一看，为了安齐，到底借需没有须要输液，以是须要那样作。
厥后那五年傍边，尔也经验了不少不少的病例，让尔感想到那一点确实是纷歧样的，最简略尔正在那面便举个小例子。
有一个孩子八岁，正在中天发热，而后呢本地以为是一个伤风，输了二地液没有睹孬，厥后便展转先到了西安一个年夜病院，而后到了南京的二野年夜病院，最初到了南京儿童病院。
到了南京儿童病院当前是他病了第七地，那个孩子很快第八地的时分便出无意识了。
而后第九地、第十地那个孩子根本上齐身皆插上管子，接上吸呼机了。
从正在本地病发，到去到南京儿童病院，野少抛却医治接归去，零十地利间，那个八岁的孩子便分开了那个世界，让尔口面有一种说没有没的感想。
从尔去那五年，像那样的案例，根本上从病发到他分开，七到十地的工夫的尔一共接触了三例，那是尔到儿童病院的感想。
赤西仁 14首 英文歌曲歌词
Yellow Gold (2)Oowah (5)Tipsy Love (8)Bass Go Boom (12)Christmas Morning (16)I.N.P (24)Adjust the love (29)Paparats (34)Hey Girl (38)My MP3 (42)RESET (45)Body talk (54)The Fifth season (56)Pindom (58)Yellow GoldSaw you there looking forNot for everything just anything that will make this life. I'm giving what you needSo just hold your hand outI can share with you, girlY our mind I need, use it to feel meTokyos gotta know yellow goldI could share with you this worldI could make you beautifulY e-ye-ye-yellow gold gold goldY ou'd better wear, wear, wear itAs your as your crown yeahY e-ye-ye-yellow gold gold goldY ou'd better wear, wear, wear itAs your as your crown yeahOhhhJust hear me follow meGotta tell you how things should be for you if you're with me This new life in TokyoCome and find it out tonightI can share with you, girlY ou could change your life with my helpNo not then, this is whenMake a change nowI could share with you this worldI said I could make you beautifulY e-ye-ye-yellow gold gold goldY ou'd better wear, wear, wear itAs your as your crown yeahY e-ye-ye-yellow gold gold goldY ou'd better wear, wear, wear itAs your as your crown yeahY ou are a diamond precious stone left aloneAll you can only be so much on your ownI'll polish your cut and set you in gold with my hands yellow bands, shiny yellow liningOh name foresee not to mean pulling inside of meWithin leaving what you needThis is my life that only I can beSo dangerous with this yellow gold thing Y e-ye-ye-yellow gold gold goldY ou'd better wear, wear, wear itAs your as your crown yeahY e-ye-ye-yellow gold gold goldY ou'd better wear, wear, wear itAs your as your crown yeahY e-ye-ye-yellow gold gold goldY ou'd better wear, wear, wear itAs your as your crown yeahY e-ye-ye-yellow gold gold goldY ou'd better wear, wear, wear itAs your as your crown yeahOowahY ou wanna count to know that how she but fly high Y eah,like a love if you that resume it multiple time What I see is something that looks just so fineAnd I say oowah, I’ll say oowahEverything is fine,I lay it on the lineI’ll be here ju st to check you only this is for tonight Y ou know I’m gonna drink like not you can remember When I call you down, and we’ll be gone now whySing it baby, you can help me say oowahHey lady, you make me wanna say oowahY ou say oowah, do it for meHey , I’m oowah, your badyNo words connect things just how I feel this loveAnd you’ll say oowah, you’ll say oowahPick a number you like,plus four and double itMinus six and divede it by the peace signLost thing you do is subtract the first number and that equals you oowahSing it baby, you can help me say oowahHey lady, you make me wanna say oowahY ou say oowah, do it for meHey , I’m oowah, your badyI wake up in the morning and I got you on my mindY ou’re all I think about ,I think about you all the tim eWaves on the beach, coconuts in the grassSweet like a lap dance spaceship blastStars in my eyes, yep , I’m standing on the moonAt times when we get a call, it’s called a buzzkillDream, money, take a load off my mindI know we never let you out of my sight girlOowahSing it baby, you can help me say oowahHey lady, you make me wanna say oowah Y ou say oowah, do it for meHey , I’m oowah, your badyOowah, I say oowahShe is so~~oh~oh~oh~ohBaby, you make me wanna say oowahY ou say oowah, you’re the m ainI’m oowah ,your babyOowah oowahOowah oowahOowahTipsy LoveIf I said do you love meWould you said Y e-ho?If I said do you need meWould you said Y e-ho?I'll keep you dry when the rain falls Cuz I've never been so enthralledDon't know howAnd I don't need nothing elseUh~Baby love can't imagineIt's like magic I found this loveBaby love can't get closerCuz you're the closest babyBaby love I got a questionDid I mention?Is this real or are we drinking our love? Y ou got me tipsy, babyIs this for real?Inebriation from this alcohol got me intoxication Y ou got me swerving from the serveAnd my cup's taken from accessAnd like a hundred dollar billI could pay for one-on-one drinkWalking down with tut, yaWanna take a shot, yaY eah, these women never take my eye off you Shots got me feeling freeAnd I'd really love to see usHolding hands and heading down the streetIf I said do you love meWould you said Y e-ho?If I said do you need meWould you said Y e-ho?I'll keep you dry when the rain fallsCuz I've never been so enthralledDon't know howAnd I don't need nothing elseUh~Baby love can't imagineIt's like magic I found this loveBaby love can't get closerCuz you're the closest babyBaby love I got a questionDid I mention?Is this real or are we drinking our love?Y ou got me tipsy, babyIs this for real?Imagination's got me thinking about this infatuationY our loving whisper has me longing for the cup of sweet rose Don't need no 100 billCuz you're the only one I'll ever needCan't believe what I just sawCrazing at you, I'm in aweI like a kurosawa pictureThere's not a single flawThen I hear my phone beepAnd I'm waking up to seeThat all of this was just another dreamIf I said do you love meWould you said Y e-ho?If I said do you need meWould you said Y e-ho?I'll keep you dry when the rain falls Cuz I've never been so enthralledDon't know howAnd I don't need nothing elseUh~Baby love can't imagineIt's like magic I found this loveBaby love can't get closerCuz you're the closest babyBaby love I got a questionDid I mention?Is this real or are we drinking our love? Y ou got me tipsy, babyBaby love can't imagineIt's like magic I found this loveBaby love can't get closerCuz you're the closest babyBaby love I got a questionDid I mention?Is this real or are we drinking our love?Y ou got me tipsy, babyBass Go BoomC.L.A.P.(We make the bass go, oh we make the bass go boom)Step in the club all the heads start turningWe bumping bottles till our vision start blurringY ou so excited that your speech starts slurringWe make the bass go, oh we make the bass go boomSo grab a pen and start learningHow Akanishi keep them records turningWe never play fair so you better be concerned whenWe make the bass go, oh we make the bass go boomI wanna see your body movingI wanna make your legs keep groovingI wanna know what you gotta do whenWe make the bass go, oh we make the bass go boomI wanna see your body movingI wanna make your legs keep groovingI wanna know what you gotta do whenWe make the bass go, oh we make the bass go boomI suppose that's cool but you know what you're drinking We taking shots till our brain stops thinkingWe so Titanic but we never be sinkingWe make the bass go, oh we make the bass go boomThat chick is giving us an eye.Our stock's so big that you know we're supplying.I think you’re in for a surprise whenWe make the bass go, oh we make the bass go boomI wanna see your body moving.I wanna make your legs keep grooving.I wanna know what you gotta do whenWe make the bass go, oh we make the bass go boomI wanna see your body movingI wanna make your legs keep groovingI wanna know what you gotta do whenWe make the bass go, oh we make the bass go boom Feel the bass go! Feel the beat go!Da da da da da da da daEh-oh! Eh-oh!So if you think you ah! came here to partyI must show you how the big boys do itFeel the bass moving through your bodyEh-oh! Eh-oh!C.L.A.P.I wanna see your body movingI wanna make your legs keep groovingI wanna know what you gotta do whenWe make the bass go, oh we make the bass go boomI wanna see your body movingI wanna make your legs keep groovingI wanna know what you gotta do whenWe make the bass go, oh we make the bass go boomI wanna see your body movingI wanna make your legs keep groovingI wanna know what you gotta do whenWe make the bass go, oh we make the bass go boomDa da da da da da da daDa da da da da da da daEh-oh! Eh-oh!Da da da da da da da daEh-oh! Eh-oh!Boom! Boom! Boom!HAC.L.A.P.Christmas MorningSnows blowing on a cold winter morning Look from you I feel my heart beating Never thought I couldn't get to youNever thought I would be with youNow I wonder how we ever could a got here Without your loving in my life my one fear Waking up without youWe changing and I know that you don't need Everything we had was all we could be Couldn't hear the words you told meI'm giving I'm giving I'm giving I'm giving I'm giving upOn youOh I've been holding back this feelingFor too long and I'm about to fall... on youI gave you I gave youAll of me all of meFirst time I saw your faceThe storms came the winds changedY ou fogged my mind with snowI'm blind nowY ou opened up the gatesWhen you came amazed meAnd now I'm drowning down down down down down We running to this beat on christmas morning Everything that I've done I've done it for youBut I know it was true the feeling was youWe running to this beat on christmas morning Everything that I've done I've done it for youBut I know it was true the feeling was youWas true was you was true was youNow I fall now you fallNow we fall togetherNow I fall now you fallNow we fall togetherNow I fall now you fallNow we fall togetherNow I fall now you falloh ohSnows blowing on a cold winter morning Look from you I feel my heart beating Never thought I couldn't get to youNever thought I would be with youNow I wonder how we ever could a got here Without your loving in my life my one fear Waking up without youWe changing and I know that you don't need Everything we had was all we could be Couldn't hear the words you told meI'm giving I'm giving I'm giving I'm giving I'm giving upOn youY ou don't know how much I sung this song Didn't know how long I left it onY ou don't know how much I sung this songDidn't know how long I left it onFirst time I saw your faceThe storms came the winds changedY ou fogged my mind with snowI'm blind nowY ou opened up the gatesWhen you came amazed meAnd now I'm drowning down down down down down We running to this beat on christmas morning Everything that I've done I've done it for you Everything that I've done I've done it for youFor ya For ya For yaWe running to this beat on christmas morning Everything that I've done I've done it for you Everything that I've done I've done it for youFor ya For ya For yaNow I fall now you fallNow we fall togetherNow I fall now you fallNow we fall togetherNow I fall now you fallNow we fall togetherNow I fall now you falloh ohKeep it upY ou gotta need it need itY ou gotta feel it feel itY ou gotta hustle move it work it and just bring that upY ou been talking all night longHow you keep your swagger onIt's time to shut your mouth and just show meY ou saying that you got the factsTo bring me where you're atY ou talking game but you can't convince meIf you got game and stacks thenTwist it and put your back inDrop it down to the floor and bring that up!If you just wanna run your mouth thenShut that up shut that upAnd if you wanna run with me thenBring that up bring that upY ou know that body's bout itY ou know how much I want itIf you wanna hit it then justBring that up bring that upY ou gotta need it need itY ou gotta feel it feel itY ou gotta hustle move it work it and just bring that upIf you ain't gotta get it outI'll show you how to move it outAll this shit you spitting want take you nowhereY ou girls been mugging all night longThey know you faded goneForget them hoes and I'll just take you thereIf you got game and stacks thenTwist it and put your back inDrop it down to the floor and bring that up!If you just wanna run your mouth thenShut that up shut that upAnd if you wanna run with me thenBring that up bring that upY ou know that body's bout itY ou know how much I want itIf you wanna hit it then justBring that up bring that upY ou gotta need it need itY ou gotta feel it feel itY ou gotta hustle move it work it and just bring that upIf you got game and stacks thenTwist it and put your back inDrop it down to the floor and bring that up!If you just wanna run your mouth thenShut that up shut that upAnd if you wanna run with me thenBring that up bring that upY ou know that body's bout itY ou know how much I want itIf you wanna hit it then justBring that up bring that upIf you just wanna run your mouth thenShut that up shut that upAnd if you wanna run with me thenBring that up bring that upY ou know that body's bout itY ou know how much I want itIf you wanna hit it then justBring that up bring that upY ou gotta need it need itY ou gotta feel it feel itY ou gotta hustle move it work it and just bring that up Bring that upI.N.PInternational party!!!It's a party take a shotIt's a party clap your handsIt's a party spend them dollarsIt's a party grab a girlIf you wanna party right gonna be a party nightBreak it down and keep it tight with that body in my sight I get money baby if you wanna come with meY ou could see how we do it in the I.N.PSo we been rocking hard it's likeWe know you want this lifeThe crystal clear is spilling hereSo come and jock a sliceSwaggin off the scale haters can study hereBut leave our differences behind we gonna party party partyuh uh uh uh uh …………………………….It's a party take a shotIt's a party clap your handsIt's a party spend them dollarsIt's a party grab a girlI can tell you how you want it to be3 peat we meet to keep the beatY ou move your feet to feel this heatIt starts to creep all empty seats Defeating beating in your chestThere's nothing left except the bestWe move we rock the beat we dropUntil on top we never stopI can tell you how you want it to be3 peat we meet to keep the beatY ou move your feet to feel this heatIt starts to creep all empty seats Defeating beating in your chestThere's nothing left except the bestWe move we rock The beat we dropUn till on top we never stopuh uh uh uh uhShorty what your name iswooooooI haven't seen you around beforewoooooooI'll show you how to partywoooooooThen shut your mouth and bust it outAnd show me how you move it babyIt's a party take a shotIt's a party clap your handsIt's a party spend them dollarsIt's a party grab a girlGirl:Up in this bitch I'm taking that toneNight of my life I'm feeling the zoneSwagger you need It you getting a loanLife's calling you boy now answer the Phone I'm Hitting it likeuh uhMy drinking is heavy your drinking is lightI'm looking for somebody better than Y ouChecking the floor and I'm wonderingWhoBoy:Up in this hoe I'm taking that toneNight of my life and I'm feeling the zoneSwagger you need It you getting a loanlife's calling you baby now answer the Phone I'm Hitting it like uh uhMy drinking is heavy your drinking is lightI'm looking for somebody better than youChecking the floor and I'm wondering whoIt's a party take a shotIt's a party clap your handsIt's a party spend them dollarsIt's a party grab a girlShorty what your name is?wooooooI haven't seen you around before woooooooI'll show you how to party woooooooThen shut your mouth and bust it out And show me how you move it baby uh uh uh uh uhIt's a party take a shotIt's a party clap your handsIt's a party spend them dollarsIt's a party grab a girlAdjust the loveFree this blood HallelujahFrom now on oh hey yoRead this book and learn your selfFrom now on We are losing track of actual loveFreedom Run to the streets and scream FreedomWe love We are losing track of actual loveAnd need to learn how to adjust loveIt's a fair well it's a good bye a time to laugh a time to love a time for us to cryIt's a fair well it's a good bye a time to laugh a time to love a time for us to cryIt's a fair well it's a good bye a time to laugh a time to love a time for us to cryIt's a fair well it's a good bye a time to laugh a time to love a time for us to cryWe be lying We crying We be standing byPeople never wanna lend a hand I'll tell you whyPeople can't get the things they need to bePeople just break your heart and then they leaveDeceiving beings surrounding me but they won't take me down cuz this spirit is freeY ou know that when you left me there was nothing for you but there was hella for mePeople lying People crying People dyeing everydayCan we figure out what the problem is with usWe move to the streets scream charity no one feeling like pushing for equalityAnd I see that the problems would beBut the pain came and the pain took me back to a placeThat I never want to go never want to seeNever want to remember the times just blinding meSo much we can strive for humanity needs to take a step forward and make a noiseAnd were poised to make a change in the universemoving for a change in the way we see this worldBefore we die let's try to make a change in the way people strive to surviveKeep the love alive till the day that we dieKilling all the reason that we got just to cryThe tears that we had to give at the timeMinds on the grind forget about the crimesFor me I'm through good byeFarewell to themI'm a always stay trueTime to laugh and time to crySo hear this song and yall write your wrongsWe can all rise aboveI am telling you now adjust your loveFreedom Run to the streets and scream FreedomWe love We are losing track of actual loveAnd need to learn how to adjust loveIt's a fair well it's a good bye a time to laugh a time to love a time for us to cryIt's a fair well it's a good bye a time to laugh a time to love a time for us to cryWe be lying we be crying we be standing byAll I want to know is why I don't hear people say I love youTell me that I love you all I want you to say is that I love youI stand alone in the zone is where you took never thought it'd take me But I know it's true cuz I look to youI pray for freedom freedom saved meBefore I'd be a slave you cold lay me in my grave go up to my Lord yes I'm a be freeChilling with our wings for all to seeHead down yonder on that grave yard walkWit the free on blast with him I'll talkNo he can't be mockedSo is it true that you reap what you sowI hope you know that sin you sowDestruction you'll be growingEven thought I know you couldn't fill my shoesY ou could fill my grave it ain't not being usedLight in hailing heck a huffing on life (abuse)Tolerance for blessing thank God every night (Stay true)Learned at a young age by the book on shelfThe book we read the truth that we tookLeft me standing staying shook I look to you my soul you tookMoving to the streets Got Revolution on my mindIn time the freedom gonna be mineDon't hide my light you watch me shineRevelation change its timeWe been dyeing it's a singWe by hungry yes indeedSo bring the rainTonight we feedWe got nothing left to sayWe got nothing left to seeWe been hungry every nightGive us everything we needTonight the night we take the leadWe break the mold we change the breedEternal life Eternally never die I'm always freeFreedom Run to the streets and scream FreedomWe love We are losing track of actual loveAnd need to learn how to adjust loveIt's a fair well it's a good bye a time to laugh a time to love a time for us to cryIt's a fair well it's a good bye a time to laugh a time to love a time for us to cryPaparatsY ou wanna get a 2nd look and take a pickKnow about my life be my guest and make it upAs long as you collect that check Y ou don'tReally give a shit do youahhhKeep it straight I'm not losing any sleepJust telling you how it isY our pictures just picturesBut they aren't worth a 1000 wordsI'm talking all about meY our articles ain't really saying shitStop wasting your time with thisLying about my lifeThis is meya ya ya yayStop wasting your timeLying about my lifeThere's no reasonsTo believe them ~let go~Just keep my nameOut your mouthIt's someone elseIt's someone elseThat's what I feelY ou failed SirA fake me you createdI'm having funThank youSee umm stop and staring everyday Trying to tear a piece of me away That's not the guy I see in the mirror That's the guy you wantThis is my life that I gaveNot what you madeThe rumors can't be trueCuz I'm a clear it up for youPaparazzi snapping shotsWriters making stories upThe proof they have is not a lot I'm living life you all forgot just taking it Day by day can you hear the things they say?This is how I do itWhen I do it cuz its my wayI can live and you can walkI can run and you can walkNobody can make a me nobody can make me stopY ou can't be replacing meThis fabrication facing meIt still entertaining meThere's no reasonsTo believe them ~let go~Just keep my nameOut your mouthIt's someone elseIt's someone elseThat's what I feelY ou failed SirA fake me you created I'm having fun Thank youIt's someone elseIt's someone else That's what I feelY ou failed SirA fake me you created I'm having fun Thank youHey GirlHey girl wanna danceIt's not youExcuse me I'm not talking to youhey girl that was youIt's you girl you girl you girlyou you you youWhoever said you were a tenMust have been counting out of a hundred thenEvery time you leave turn around baby come back to me Before you break my heart so uglyBut we drunk so I guess It's cool with meAnd I never joke but I love jkNot the funny girls but ones that say UchyoAnd what I'm saying is so superSo I guess that makes me super sayingSuper star, hide the lids so you don't know who we areSo show me how we sipping parties tripping when we kicking itSo hey girl your sisters looking dopeSo excuse me Miss let me through cuz I got something to say I'm not talking to you !Hey girl wanna danceIt's not youExcuse me I'm not talking to youHey girl that was youIt's you girl you girl you girlyou you you youWhoever said you were a tenMust have been counting out of a hundred thenI'm so fxxked up turn the party upTill we all puke up we change that upEvery time I'm here I'm staring at herShe looks really hot from far awayBut when you get close she is far away from hot (shit!)Her name is XXXX she is a bartender on the 2nd floorSo that's why I don't wanna go up thereExcuse me girl you wanna dance with meY ou wanna drink with me as usually I'm trying to get a check with those typical linesOMG here comes gold digger diggerHold champagne and drinking jaguar jaguarI hate that thing I'm drunk I thinkBounce out this spot I need ladiesHey girl wanna danceIt's not youExcuse me I'm not talking to youHey girl that was youIt's you girl you girl you girlOh snap I think I found the oneWish I could be that straw on your tongueY o how ya doing girl my name is JinLet me play in your game I swear ill winThat made her grin I think I'm inLet's have a drink and chill for a bitTell me your name cuz I did the same show some lovefor we out this clubHer friends are pissed my friends are madWe spending time gonna call a cabTill my homi tripped and spilled his glassShe's soaked with beer an bouncing out a hereIt's aight ya see cuz I didn't really needAnything from her Know could a done better Letter go Get another few mins you already knowI'll find a better hoeHey girl wanna danceIt's not youExcuse me I'm not talking to youHey girl that was youIt's you girl you girl you girlHey girl wanna danceIt's not youExcuse me I'm not talking to youHey girl that was youIt's you girl you girl you girlLa la la la la la la la...Whoever said you were a tenMust have been counting out of a hundred then My MP3Y ou know I feel your beat inside my mindY ou know your tempos just a little highThe way your bass is bumping I need moreI love the way you always have a rhymeAn how your words fit so perfect with mineIt's time to press play on this girlAn will dance until we can't take any moreThis sweet song is my m-p-p-p-3The way I feel herbeat-beat-beat-beat-beatThis song I guess I need need need need needLa la la lasweet sweet sweet sweetY our eyes have got to just be synthesizedY ou're sweeter than the first verse with a 9th Now the second verse starts to blend with mine La la la la la laI'll find a way to keep this mp3An play it in my life for eternityBetter than you've ever had beforeKeep the bass rockingWanting moreBecause....This sweet song is my m-p-p-p-3The way I feel herbeat-beat-beat-beat-beatThis song I guess I need need need need needLa la la lasweet sweet sweet sweetTurn it up or turn it downThe beat is bumping this whole damn town Like a ghetto blaster of the groundIt's pounds and pounds and pounds and poundsThis sweet song is my m-p-p-p-3The way I feel herbeat-beat-beat-beat-beatThis song I guess I need need need need need La la la laThis sweet song is my m-p-p-p-3The way I feel herbeat-beat-beat-beat-beatThis song I guess I need need need need needLa la la lasweet sweet sweet sweetRESETPieces of lives we rememberPieces of lives we won't forgetoh oh ohDown cuz we gonna go and reset life nowPieces of our lives we rememberPieces of our lives we won't forgetoh oh ohDown cuz we gonna go and reset life nowDid you ever wonder if you would forget the sunshineI know you'd always be mine I think about it from time to time I know we'd never have these problems looking at you everyday I never thought I'd ever have to hear you ever have to say Words that you don't know the things that you don't wanna know Things I told you when I told you and I never let you knowY ou told me once or twice the things we had to see。
《想飞的钢琴少年》经典台词
《想飞的钢琴少年》经典台词篇一：《会飞的钢琴少年》观后感《想飞的钢琴少年》观后感佛瑞迪.穆勒导演的瑞士影片《想飞的钢琴少年》讲述了一个关于音乐神童维特的人生故事。
影片中维特的母亲也许是爱子心切，总是希望能够挖掘和培养维特超常的潜能，希望能将维特培养成为一名出色的钢琴师。
所以，她的一切活动都是围绕这一切来展开：给维特更换更好的钢琴老师；全职在家做维特的“保姆”；找著名的钢琴家做维特的老师；监督维特每天弹钢琴；让维特上成人音乐学院??就是这样的对维特近乎全方位的“监控”。
其实维特对周围所有的事情都好奇，他想学习的不只是弹钢琴，他想学习许许多多的事情：数学、炒股??而母亲只让他在钢琴上发展。
终于小维特受不了了，在一个雷雨交加的晚上纵身一跃??幸运的是，小维特因为有“翅膀”的保护只是受到了一点点的伤。
但这一跳，维特的大脑受损，维特变成了一个很普通的孩子，他转到了一个很普通的学校和普通的班级，和普通的同龄孩子一起学习玩耍，做12岁的小孩子喜欢做的事情，这正是维特想要的。
后来当维特发现爷爷和父母的经济都已陷入了窘境，父亲的公司股价将急剧降低。
他开始不再欺骗人们，开始研究股市，并与爷爷合作，利用爷爷的全部家当成功赚取了上百万的钱。
并以沃夫博士的名字成为了股市炙手可热的人物。
父亲被解雇，维特找来了自己母亲的朋友，将一切对她全盘托出，并任命她为沃夫控股公司CEO，让她帮助自己收购父亲的公司，并让父亲做了总裁。
故事的结局是美好的，维特在钢琴上大获成功，也圆了自己翱翔蓝天的梦想。
喜欢音乐，喜欢钢琴乐曲，对主人公精湛的弹奏技艺更是赞叹不已，但更多是维特这个孩子引起我深深的思考。
维特是一个超常儿童，逻辑思维强，思维敏捷，思维广阔且有独创性，有很强的问题解决能力。
他能解决个人生理发展与心理发展的矛盾、个人认知发展与人格发展的矛盾、个人人生理想与个人现实条件的矛盾。
不过超常儿童几乎是总是孤独的，虽然最好的伙伴就是自己的父母亲，但和父母相互理解的又有几何呢？生活中遇到的多数都是普通的孩子，和多数妈妈一样，将自己或大伙儿觉得时下必须的要求孩子学习，满足一己私心，往往没有考虑孩子的感受，令他们不满甚至逃避。
电台讲座
电台讲座.txt49礁石因为信念坚定，才激起了美丽的浪花；青春因为追求崇高，才格外地绚丽多彩。
50因为年轻，所以自信；因为自信，所以年轻。
神奇蛇疗--蛇之语电台讲座素材《神奇蛇疗—蛇之语风湿骨病健康聚焦栏目》蛇之语---走进蛇疗抗风湿特别节目（电台素材）主持人：听众朋友大家好，欢迎收听本期走进蛇疗---抗风湿专题栏目。
提到蛇大家都会胆战心惊，今天我们就和大家谈的问题，偏偏就是和蛇有关的话题，说的是风湿骨病治疗领域的一项最新突破---蛇疗，我们希望通过今天的节目，能让您和您的家人早一天从风湿病的痛苦中解脱出来。
这个风湿和类风湿又被称为不死的癌症，一直以来困扰着很多的患者和家庭，它的病情是复杂多变的，极易严重致残。
最近一位家在天津的刘顺昌大爷，给我们节目组寄来了一封信。
（讲故事案例，引出两位专家的案例分析）说他今年62岁了，年轻的时候上山下乡去了北大荒，在那一干就干了10年开垦湿地的活。
因为他的腿脚经常泡在水里，到了30多岁的时候呢，他就得了风湿病，那么近几年他经常会感觉到骨头里有一块散发着一股寒气的千年寒冰，患病20多年李大爷吃了不少的药，也看了不少的医生，但是都没有治好他的病。
没想到，前不久却被中国蛇疗大王---杨洪昌博士，特殊的三条蛇给弄好了，今天我们就请来了两位专家，来跟我们谈一谈这三条蛇是怎么治好刘大爷的病的。
一位是我们中国著名的风湿骨病专家李玉臻主任，（大家好）另一位是中国蛇疗大王，杨洪昌博士（大家好）欢迎二位专家来到我们的演播室，两位专家我们不难想象像刘大爷这样20多年的老风湿病患者在他的患病期间肯定是吃了不少的药，看了不少的医生，最终都没有治好他的风湿病，这中间的原因到底是什么呢？？专家1李玉臻：刘大爷这个病之所以是反反复复久治不愈，他就是因为从前的治疗方法，它是治标不治本。
现代中医理论认为，骨与筋的关系非常密切，筋指肌腱，附于骨关节的叫筋，包于肌腱外的叫筋膜，筋膜分浅筋膜与深筋膜两种。
辅酶Q10 的讲稿
辅酶Q10与心脏1、一切从心开始XX，让我们一起来学习有关心脏方面的知识，如果把这些知识学好了，一定会对您有很大的帮助。
心脏健康是人类健康的基石，心脏健康了，才能有充足的血液供应给其他器官，器官才能健康。
但是，目前心脏病是人类健康的第一杀手，每一个人听到心脏病都会害怕，美国人称心脏病为时代的瘟疫。
所以健康必须从心开始，我们一定要留心、爱心、护心、欢心，让我们的心脏可以健康跳下去。
您说好吗？2、心脏，人体的发动机那么心脏在人体当中起什么作用呢？打个比喻，如果把人体比喻成一部汽车，那么心脏就是发动机，发动机正常工作，汽车才可以行使，如果发动机坏了，车就开不动了，人也一样，心脏停止跳动，生命就终止了。
3、心脏为君主之官西医把心脏比喻成发动机，那么中医呢？中医认为心为君主之官。
如果把人比喻成一个国家，五脏六腑就是官员，心脏就是君主，肝就是将军，肺就是丞相，一个国家的兴衰跟领导人有直接的关系，如果一个领导人无能或者腐败，这个国家就会走向衰落，直至灭亡。
同样的道理，一个人健康的好坏跟心脏有很大关系，如果心脏有问题全身都会有问题，心脏健康人也更健康。
4、心脏外表形象您有见过真人心脏吗？猪心应该见过吧。
您知道心脏有多大吗？请举起拳头，通常和本人拳头差不多大，它位于胸腔内两肺之间，略偏左，心尖位于第5—6肋骨之间。
5、心路历程您知道心脏什么时候开始跳动吗？50天的胎儿心脏就开始跳动了，直到人生的最后一刻，从未休息过。
心脏是功劳最大的脏腑同时又是最疲劳的器官，心脏每天跳动约10万次，到80岁时心脏跳动约30亿次。
有人计算过，心脏一生所做的功相当于一个人把3万公斤的水举到珠穆朗玛峰。
但是为什么现在这么多人出现了心脏意外呢？为什么很多人年纪轻轻就猝死了呢？为什么心脏病是第一杀手呢？那是因为心脏从未保养过，它太疲劳了。
6、每时每刻都离不开心脏每个器官、每个细胞。
每时每刻都离不开心脏，就像鱼儿离不开水一样。
心脏不能供应充足的血液给脑部，就会出现头晕、头痛、失眠、脑坏死等严重问题发生。
欧洲药典索引版3
EUROPEAN PHARMACOPOEIA5.5INDEXTo aid users the index includes a reference to the supplement where the latest version of a text can be found.For example:Acetone...............................................5.1-2875means the monograph Acetone can be found on page2875of Supplement5.1.Note that where no reference for a supplement is made,the text can be found in the principal volume.Monographs deleted from the5th edition are not included in the index;the list of deleted texts is found in the Contents of this supplement,page xxx.EUROPEAN PHARMACOPOEIA5.5Numerics1.1.General statements (5)1.2.Other provisions applying to general chapters and monographs (5)1.3.General chapters (6)1.4.Monographs (7)1.5.Abbreviations and symbols (9)1.6.Units of the International System(SI)used in the Pharmacopoeia and equivalence with other units (10)1.General notices (5)2.1.1.Droppers (17)parative table of porosity of sintered-glass filters (17)2.1.3.Ultraviolet ray lamps for analytical purposes (17)2.1.4.Sieves (18)2.1.5.Tubes for comparative tests (19)2.1.6.Gas detector tubes (19)2.1.Apparatus (17)2.2.10.Viscosity-Rotating viscometer method.........5.3-3337 2.2.11.Distillation range (30)2.2.12.Boiling point (31)2.2.13.Determination of water by distillation (32)2.2.14.Melting point-capillary method (32)2.2.15.Melting point-open capillary method (33)2.2.16.Melting point-instantaneous method (33)2.2.17.Drop point (33)2.2.18.Freezing point (34)2.2.19.Amperometric titration (34)2.2.1.Clarity and degree of opalescence of liquids (23)2.2.20.Potentiometric titration (35)2.2.21.Fluorimetry (35)2.2.22.Atomic emission spectrometry (35)2.2.23.Atomic absorption spectrometry (36)2.2.24.Absorption spectrophotometry,infrared (37)2.2.25.Absorption spectrophotometry,ultraviolet and visible.................................................................................5.2-3089 2.2.26.Paper chromatography. (40)2.2.27.Thin-layer chromatography...............................5.2-3090 2.2.28.Gas chromatography.. (42)2.2.29.Liquid chromatography (43)2.2.2.Degree of coloration of liquids (24)2.2.30.Size-exclusion chromatography (45)2.2.31.Electrophoresis (45)2.2.32.Loss on drying (50)2.2.33.Nuclear magnetic resonance spectrometry (51)2.2.34.Thermal analysis (52)2.2.35.Osmolality (54)2.2.36.Potentiometric determination of ionic concentration using ion-selective electrodes (55)2.2.37.X-ray fluorescence spectrometry (56)2.2.38.Conductivity.........................................................5.1-2783 2.2.39.Molecular mass distribution in dextrans (57)2.2.3.Potentiometric determination of pH (26)2.2.40.Near-infrared spectrophotometry (59)2.2.41.Circular dichroism (63)2.2.42.Density of solids (64)2.2.43.Mass spectrometry (65)2.2.44.Total organic carbon in water for pharmaceutical use (68)2.2.45.Supercritical fluid chromatography (68)2.2.46.Chromatographic separation techniques (69)2.2.47.Capillary electrophoresis (74)2.2.48.Raman spectrometry (79)2.2.49.Falling ball viscometer method (80)2.2.4.Relationship between reaction of solution, approximate pH and colour of certain indicators (27)2.2.54.Isoelectric focusing (81)2.2.55.Peptide mapping (82)2.2.56.Amino acid analysis.......................................................862.2.5.Relative density.. (27)2.2.6.Refractive index (28)2.2.7.Optical rotation......................................................5.4-3695 2.2.8.Viscosity (29)2.2.9.Capillary viscometer method (29)2.2.Physical and physicochemical methods (23)2.3.1.Identification reactions of ions and functional groups...............................................................................5.5-4101 2.3.2.Identification of fatty oils by thin-layer chromatography. (98)2.3.3.Identification of phenothiazines by thin-layer chromatography (99)2.3.4.Odour (99)2.3.Identification (95)2.4.10.Lead in sugars (107)2.4.11.Phosphates (108)2.4.12.Potassium (108)2.4.13.Sulphates (108)2.4.14.Sulphated ash......................................................5.3-3341 2.4.15.Nickel in polyols.. (108)2.4.16.Total ash (108)2.4.17.Aluminium (108)2.4.18.Free formaldehyde (109)2.4.19.Alkaline impurities in fatty oils (109)2.4.1.Ammonium (103)2.4.21.Foreign oils in fatty oils by thin-layer chromatography (109)position of fatty acids by gas chroma-tography (110)2.4.23.Sterols in fatty oils..............................................5.1-2787 2.4.24.Identification and control of residual solvents (113)2.4.25.Ethylene oxide and dioxan (118)2.4.26.N,N-Dimethylaniline (119)2.4.27.Heavy metals in herbal drugs and fatty oils (119)2.4.28.2-Ethylhexanoic acid (120)position of fatty acids in oils rich inomega-3-acids...................................................................5.5-4107 2.4.2.Arsenic (103)2.4.30.Ethylene glycol and diethylene glycol in ethoxylated substances........................................................................5.2-3095 2.4.3.Calcium.. (103)2.4.4.Chlorides (104)2.4.5.Fluorides (104)2.4.6.Magnesium (104)2.4.7.Magnesium and alkaline-earth metals (104)2.4.8.Heavy metals (104)2.4.9.Iron (107)2.4.Limit tests (103)2.5.10.Oxygen-flask method (130)plexometric titrations (130)2.5.12.Water:semi-micro determination (130)2.5.13.Aluminium in adsorbed vaccines (131)2.5.14.Calcium in adsorbed vaccines (131)2.5.15.Phenol in immunosera and vaccines (131)2.5.16.Protein in polysaccharide vaccines (131)2.5.17.Nucleic acids in polysaccharide vaccines (132)2.5.18.Phosphorus in polysaccharide vaccines (132)2.5.19.O-Acetyl in polysaccharide vaccines (132)2.5.1.Acid value................................................................5.2-3099 2.5.20.Hexosamines in polysaccharide vaccines. (132)2.5.21.Methylpentoses in polysaccharide vaccines (133)2.5.22.Uronic acids in polysaccharide vaccines (133)2.5.23.Sialic acid in polysaccharide vaccines (133)2.5.24.Carbon dioxide in gases (134)2.5.25.Carbon monoxide in gases (134)2.5.26.Nitrogen monoxide and nitrogen dioxide in gases (135)2.5.27.Oxygen in gases (136)2.5.28.Water in gases (136)2.5.29.Sulphur dioxide (136)2.5.2.Ester value (127)2.5.30.Oxidising substances (137)2.5.31.Ribose in polysaccharide vaccines (137)2.5.32.Water:micro determination (137)2.5.33.Total protein (138)2.5.34.Acetic acid in synthetic peptides (141)2.5.35.Nitrous oxide in gases (141)2.5.36.Anisidine value (142)2.5.3.Hydroxyl value (127)2.5.4.Iodine value (127)2.5.5.Peroxide value (128)2.5.6.Saponification value (129)2.5.7.Unsaponifiable matter (129)2.5.8.Determination of primary aromaticamino-nitrogen (129)2.5.9.Determination of nitrogen by sulphuric acid digestion (129)2.5.Assays (127)2.6.10.Histamine (153)2.6.11.Depressor substances (153)2.6.12.Microbiological examination of non-sterile products (total viable aerobic count) (154)2.6.13.Microbiological examination of non-sterile products (test for specified micro-organisms) (156)2.6.14.Bacterial endotoxins (161)2.6.15.Prekallikrein activator........................................5.5-4111 2.6.16.Tests for extraneous agents in viral vaccines for human use (169)2.6.17.Test for anticomplementary activity of immunoglobulin (170)2.6.18.Test for neurovirulence of live virus vaccines (172)2.6.19.Test for neurovirulence of poliomyelitis vaccine (oral) (172)2.6.1.Sterility (145)2.6.20.Anti-A and anti-B haemagglutinins(indirect method) (174)2.6.21.Nucleic acid amplification techniques............5.5-4111 2.6.22.Activated coagulation factors...........................5.5-4115 2.6.24.Avian viral vaccines:tests for extraneous agents in seed lots............................................................................5.4-3699 2.6.25.Avian live virus vaccines:tests for extraneous agents in batches of finished product.....................................5.3-3345 2.6.26.Test for anti-D antibodies in human immunoglobulin for intravenous administration....................................5.3-3348 2.6.2.Mycobacteria. (149)2.6.7.Mycoplasmas (149)2.6.8.Pyrogens (152)2.6.9.Abnormal toxicity (153)2.6.Biological tests (145)2.7.10.Assay of human coagulation factor VII (203)2.7.11.Assay of human coagulation factor IX............5.5-4120 2.7.12.Assay of heparin in coagulation factors (204)2.7.13.Assay of human anti-D immunoglobulin (205)2.7.14.Assay of hepatitis A vaccine..............................5.1-2795 2.7.15.Assay of hepatitis B vaccine(rDNA). (207)2.7.16.Assay of pertussis vaccine(acellular) (208)2.7.17.Assay of human antithrombin III (209)2.7.18.Assay of human coagulation factor II (209)2.7.19.Assay of human coagulation factor X (210)2.7.1.Immunochemical methods (187)2.7.20.In vivo assay of poliomyelitis vaccine (inactivated) (210)2.7.21.Assay of human von Willebrand factor...........5.5-4120 2.7.22.Assay of human coagulation factor XI............5.5-4121 2.7.2.Microbiological assay of antibiotics. (188)2.7.4.Assay of human coagulation factor VIII...........5.5-4119 2.7.5.Assay of heparin.. (195)2.7.6.Assay of diphtheria vaccine(adsorbed).....................1962.7.7.Assay of pertussis vaccine (197)2.7.8.Assay of tetanus vaccine(adsorbed)..................5.1-2791 2.7.9.Test for Fc function of immunoglobulin. (202)2.7.Biological assays (187)2.8.10.Solubility in alcohol of essential oils (216)2.8.11.Assay of1,8-cineole in essential oils (216)2.8.12.Determination of essential oils in vegetable drugs (217)2.8.13.Pesticide residues (218)2.8.14.Determination of tannins in herbal drugs (221)2.8.15.Bitterness value (221)2.8.16.Dry residue of extracts (222)2.8.17.Loss on drying of extracts (222)2.8.1.Ash insoluble in hydrochloric acid (215)2.8.2.Foreign matter (215)2.8.3.Stomata and stomatal index (215)2.8.4.Swelling index (215)2.8.5.Water in essential oils (216)2.8.6.Foreign esters in essential oils (216)2.8.7.Fatty oils and resinified essential oils in essential oils (216)2.8.8.Odour and taste of essential oils (216)2.8.9.Residue on evaporation of essential oils (216)2.8.Methods in pharmacognosy (215)2.9.10.Ethanol content and alcoholimetric tables (237)2.9.11.Test for methanol and2-propanol...................5.3-3362 2.9.12.Sieve test (239)2.9.13.Limit test of particle size by microscopy (239)2.9.14.Specific surface area by air permeability (239)2.9.15.Apparent volume (241)2.9.16.Flowability (242)2.9.17.Test for extractable volume of parenteral preparations.....................................................................5.3-3363 2.9.18.Preparations for inhalation:aerodynamic assessment of fine particles...............................................................5.2-3103 2.9.19.Particulate contamination:sub-visible particles (253)2.9.1.Disintegration of tablets and capsules..............5.3-3351 2.9.20.Particulate contamination:visible particles. (255)2.9.22.Softening time determination of lipophilic suppositories (256)2.9.23.Pycnometric density of solids (257)2.9.24.Resistance to rupture of suppositories and pessaries (258)2.9.25.Dissolution test for medicated chewing gums..................................................................................5.2-3116 2.9.26.Specific surface area by gas adsorption.........5.1-2811 2.9.27.Uniformity of mass of delivered doses from multidose containers. (263)2.9.28.Test for deliverable mass or volume of liquid and semi-solid preparations (263)2.9.29.Intrinsic dissolution............................................5.4-3705 2.9.2.Disintegration of suppositories and pessaries (227)2.9.36.Powder flow..........................................................5.3-3363 2.9.37.Optical microscopy..............................................5.3-3366 2.9.38.Particle-size distribution estimation by analytical sieving...............................................................................5.3-3368 2.9.3.Dissolution test for solid dosage forms............5.3-3353 2.9.40.Uniformity of dosage units................................5.3-3370 2.9.42.Dissolution test for lipophilic solid dosage forms..................................................................................5.3-3373 2.9.4.Dissolution test for transdermal patches (231)2.9.5.Uniformity of mass of single-dose preparations (233)2.9.6.Uniformity of content of single-dose preparations..234 2.9.7.Friability of uncoated tablets..............................5.2-3103 2.9.8.Resistance to crushing of tablets.. (235)2.9.9.Measurement of consistency by penetrometry (235)2.9.Pharmaceutical technical procedures (225)3.1.10.Materials based on non-plasticised poly(vinyl chloride) for containers for non-injectable,aqueous solutions (289)3.1.11.Materials based on non-plasticised poly(vinyl chloride)for containers for dry dosage forms for oral administration..........................................................................2913.1.1.1.Materials based on plasticised poly(vinyl chloride)for containers for human blood and blood components. (269)3.1.1.2.Materials based on plasticised poly(vinyl chloride)for tubing used in sets for the transfusion of blood andblood components (272)3.1.13.Plastic additives (293)3.1.14.Materials based on plasticised poly(vinyl chloride)for containers for aqueous solutions for intravenous infusion......................................................................................2963.1.15.Polyethyleneterephthalatefor containers forpreparations not for parenteral use.....................................2983.1.1.Materials for containers for human blood and blood components. (269)3.1.3.Polyolefines (274)3.1.4.Polyethylene without additives for containers for parenteral preparations and for ophthalmic preparations..............................................................................2783.1.5.Polyethylene with additives for containers for parenteral preparations and for ophthalmicpreparations..............................................................................2793.1.6.Polypropylene for containers and closures for parenteral preparationsand ophthalmic preparations (282)3.1.7.Poly(ethylene -vinyl acetate)for containers and tubing for total parenteral nutrition preparations........................2853.1.8.Silicone oilused as a lubricant (287)3.1.9.Silicone elastomer for closures and tubing..............2883.1.Materials used for the manufacture of containers.....2693.2.1.Glass containers for pharmaceutical use..................3033.2.2.1.Plastic containers for aqueous solutions for parenteral infusion..................................................................3093.2.2.Plastic containers and closures for pharmaceuticaluse...............................................................................................3083.2.3.Sterile plastic containers for human blood and bloodcomponents...............................................................................3093.2.4.Empty sterile containers of plasticised poly(vinylchloride)forhuman blood and blood components...........3113.2.5.Sterile containers of plasticisedpoly (vinylchloride)for human blood containing anticoagulant solution.......3123.2.6.Sets for the transfusion of blood and blood components................................................................................3133.2.8.Sterile single-use plastic syringes................................3143.2.9.Rubber closures for containers for aqueous parenteral preparations,for powders and for freeze-dried powders..3163.2.Containers...........................................................................3034.1.1.Reagents..................................................................5.4-37094.1.1.Reagents..................................................................5.5-41254.1.2.Standard solutions for limit tests.......................5.4-38174.1.2.Standard solutions for limit tests.......................5.5-41264.1.3.Buffer solutions.....................................................5.4-38214.1.3.Buffer solutions.....................................................5.5-41264.1.Reagents,standard solutions,buffer solutions..5.4-37094.2.1.Primary standards for volumetric solutions....5.4-38274.2.2.Volumetric solutions.............................................5.4-38274.2.2.Volumetric solutions.............................................5.5-41274.2.Volumetric analysis...................................................5.4-38274.Reagents.........................................................................5.4-37095.10.Control of impurities in substances for pharmaceuticaluse......................................................................................5.5-41455.11.Characters section in monographs (565)5.1.1.Methods of preparation of sterile products..............4455.1.2.Biological indicators of sterilisation (447)5.1.3.Efficacy of antimicrobial preservation.......................4475.1.4.Microbiological quality of pharmaceuticalpreparations (449)5.1.5.Application of the F 0concept to steam sterilisation of aqueous preparations....................................................5.1-2821 5.1.6.Alternative methods for control of microbiological quality................................................................................5.5-41315.1.Generaltexts onsterility..................................................4455.2.1.Terminology used in monographs on vaccines (453)5.2.2.Chicken flocks free from specified pathogens for the production and quality control of vaccines...............5.1-28255.2.3.Cell substrates for the production of vaccines for human use.................................................................................4555.2.4.Cell cultures for the production of veterinaryvaccines (458)5.2.5.Substances of animal origin for the production ofveterinary vaccines (460)5.2.6.Evaluation of safety of veterinary vaccines andimmunosera ....................................................................5.1-28275.2.7.Evaluation of efficacy of veterinary vaccines and immunosera.....................................................................5.1-28295.2.8.Minimising the risk of transmitting animal spongiform encephalopathy agents via human and veterinary medicinal products (463)5.2.9.Evaluation of safety of each batch of veterinary vaccines and immunosera.............................................5.1-28305.2.General texts on vaccines (453)5.3.Statistical analysis of results of biological assays andtests (475)5.4.Residual solvents...............................................................5075.5.Alcoholimetric tables.........................................................5195.6.Assay of interferons..................................................5.3-33815.7.Table of physical characteristics of radionuclidesmentioned in the European Pharmacopoeia.....................5395.8.Pharmacopoeial harmonisation.....................................5515.9.Polymorphism (555)AAbbreviationsand symbols (1.5.) (9)Abnormal toxicity (2.6.9.) (153)Absinthiiherba ........................................................................2710Absorption spectrophotometry,infrared (2.2.24.). (37)Absorption spectrophotometry,ultraviolet and visible (2.2.25.).............................................................................5.2-3089Acacia (905)Acaciae gummi (905)Acaciae gummi dispersione desiccatum .............................905Acacia,spray-dried (905)Acamprosate calcium................................................................906Acamprosatum calcicum (906)Acarbose..............................................................................5.1-2873Acarbosum .........................................................................5.1-2873Acebutololhydrochloride................................................5.4-3889Acebutololi hydrochloridum .........................................5.4-3889Aceclofenac (909)Aceclofenacum (909)Acesulfame potassium.....................................................5.4-3890Acesulfamum kalicum ....................................................5.4-3890Acetazolamide (912)Acetazolamidum (912)Acetic acid,glacial (913)Acetic acid in synthetic peptides (2.5.34.) (141)Acetone................................................................................5.1-2875Acetonum ...........................................................................5.1-2875Acetylcholine chloride...............................................................914Acetylcholini chloridum .. (914)Acetylcysteine..............................................................................915Acetylcysteinum (915)β-Acetyldigoxin..................................................................5.5-4185β-Acetyldigoxinum ...........................................................5.5-4185Acetylsalicylic acid (917)Acetyltryptophan,N - (918)Acetyltyrosine,N - (920)Aciclovir..............................................................................5.3-3436Aciclovirum.......................................................................5.3-3436 Acidum4-aminobenzoicum (973)Acidum aceticum glaciale (913)Acidum acetylsalicylicum (917)Acidum adipicum (926)Acidum alginicum (942)Acidum amidotrizoicum dihydricum (967)Acidum aminocaproicum (974)Acidum ascorbicum (1025)Acidum asparticum (1029)Acidum benzoicum (1072)Acidum boricum (1117)Acidum caprylicum (1172)Acidum chenodeoxycholicum (1247)Acidum citricum anhydricum (1306)Acidum citricum monohydricum (1307)Acidum edeticum.............................................................5.4-3933 Acidum etacrynicum.. (1542)Acidum folicum (1630)Acidum fusidicum (1645)Acidum glutamicum (1670)Acidum hydrochloridum concentratum (1755)Acidum hydrochloridum dilutum (1756)Acidum iopanoicum (1824)Acidum iotalamicum (1825)Acidum ioxaglicum (1826)Acidum lacticum..............................................................5.2-3227 Acidum lactobionicum.. (1885)Acidum maleicum (1966)Acidum malicum (1966)Acidum mefenamicum (1984)Acidum methacrylicum et ethylis acrylas polymerisatum 1:1 (2005)Acidum methacrylicum et ethylis acrylas polymerisatum 1:1dispersio30per centum (2005)Acidum methacrylicum et methylis methacrylas polymerisatum1:1 (2006)Acidum methacrylicum et methylis methacrylas polymerisatum1:2 (2007)Acidum nalidixicum (2080)Acidum nicotinicum (2097)Acidum nitricum (2105)Acidum oleicum (2132)Acidum oxolinicum (2165)Acidum palmiticum (2179)Acidum phosphoricum concentratum (2237)Acidum phosphoricum dilutum (2238)Acidum pipemidicum trihydricum (2249)Acidum salicylicum.........................................................5.1-3007 Acidum(S)-lacticum........................................................5.2-3227 Acidum sorbicum.. (2467)Acidum stearicum (2490)Acidum sulfuricum (2520)Acidum tartaricum (2534)Acidum thiocticum...........................................................5.5-4312 Acidum tiaprofenicum.. (2578)Acidum tolfenamicum (2601)Acidum tranexamicum (2609)Acidum trichloraceticum (2620)Acidum undecylenicum (2658)Acidum ursodeoxycholicum (2662)Acidum valproicum (2669)Acid value(2.5.1.)..............................................................5.2-3099 Acitretin. (922)Acitretinum (922)Acriflavinii monochloridum (924)Acriflavinium monochloride (924)Actinobacillosis vaccine(inactivated),porcine (784)Activated charcoal....................................................................1246Activated coagulation factors(2.6.22.).........................5.5-4115 Additives,plastic(3.1.13.) (293)Adenine (924)Adeninum (924)Adenosine (925)Adenosinum (925)Adeps lanae.......................................................................5.2-3285 Adeps lanae cum aqua.. (2709)Adeps lanae hydrogenatus (2708)Adeps solidus (1711)Adipic acid (926)Adrenaline tartrate (927)Adrenalini tartras (927)Aer medicinalis (929)Aer medicinalis artificiosus (932)Aerodynamic assessment of fine particles in preparations for inhalation(2.9.18.).........................................................5.2-3103 Aether.. (1548)Aether anaestheticus (1549)Agar (928)Agni casti fructus.............................................................5.4-3892 Agnus castus fruit.............................................................5.4-3892 Agrimoniae herba (929)Agrimony (929)Air,medicinal (929)Air,synthetic medicinal (932)Alanine (933)Alaninum (933)Albendazole (934)Albendazolum (934)Albumini humani solutio...............................................5.3-3511 Albumin solution,human................................................5.3-3511 Alchemilla (935)Alchemillae herba (935)Alcohol benzylicus...........................................................5.5-4197 Alcohol cetylicus...............................................................5.3-3475 Alcohol cetylicus et stearylicus....................................5.3-3474 Alcohol cetylicus et stearylicus emulsificans A.. (1239)Alcohol cetylicus et stearylicus emulsificans B (1241)Alcoholes adipis lanae (2703)Alcoholimetric tables(2.9.10.) (237)Alcoholimetric tables(5.5.) (519)Alcohol isopropylicus (1841)Alcohol oleicus (2134)Alcohol stearylicus...........................................................5.3-3621 Alcuronii chloridum.. (935)Alcuronium chloride (935)Alexandrian senna pods (2404)Alfacalcidol (937)Alfacalcidolum (937)Alfadex (938)Alfadexum (938)Alfentanil hydrochloride (939)Alfentanili hydrochloridum (939)Alfuzosin hydrochloride (941)Alfuzosini hydrochloridum (941)Alginic acid (942)Alkaline-earth metals and magnesium(2.4.7.) (104)Alkaline impurities in fatty oils(2.4.19.) (109)Allantoin (942)Allantoinum (942)Allergen products (569)Allii sativi bulbi pulvis (1651)Allium sativum ad praeparationes homoeopathicas (897)Allopurinol (943)Allopurinolum (943)all-rac-α-Tocopherol..........................................................5.5-4313 all-rac-α-Tocopheryl acetate...........................................5.5-4314 Almagate.............................................................................5.2-3169Almagatum.........................................................................5.2-3169 Almond oil,refined...........................................................5.4-3893 Almond oil,virgin.............................................................5.3-3437 Aloe barbadensis.. (947)Aloe capensis (948)Aloes,barbados (947)Aloes,Cape (948)Aloes dry extract,standardised (949)Aloes extractum siccum normatum (949)Alphacyclodextrin (938)Alprazolam (950)Alprazolamum (950)Alprenolol hydrochloride (952)Alprenololi hydrochloridum (952)Alprostadil (953)Alprostadilum (953)Alteplase for injection (956)Alteplasum ad iniectabile (956)Alternative methods for control of microbiological quality (5.1.6.)................................................................................5.5-4131 Althaeae folium (1974)Althaeae radix...................................................................5.2-3232 Alum. (959)Alumen (959)Aluminii chloridum hexahydricum (960)Aluminii hydroxidum hydricum ad adsorptionem..5.5-4186 Aluminii magnesii silicas (961)Aluminii oxidum hydricum (962)Aluminii phosphas hydricus (963)Aluminii phosphatis liquamen.....................................5.3-3438 Aluminii sulfas (964)Aluminium(2.4.17.) (108)Aluminium chloride hexahydrate (960)Aluminium hydroxide,hydrated,for adsorption........5.5-4186 Aluminium in adsorbed vaccines(2.5.13.).. (131)Aluminium magnesium silicate (961)Aluminium oxide,hydrated (962)Aluminium phosphate gel...............................................5.3-3438 Aluminium phosphate,hydrated.. (963)Aluminium sulphate (964)Amantadine hydrochloride (964)Amantadini hydrochloridum (964)Ambroxol hydrochloride (965)Ambroxoli hydrochloridum (965)Amfetamine sulphate (966)Amfetamini sulfas (966)Amidotrizoic acid dihydrate (967)Amikacin (968)Amikacini sulfas...............................................................5.4-3894 Amikacin sulphate............................................................5.4-3894 Amikacinum. (968)Amiloride hydrochloride..................................................5.3-3439 Amiloridi hydrochloridum.............................................5.3-3439 Amino acid analysis(2.2.56.).. (86)Aminobenzoic acid,4- (973)Aminocaproic acid (974)Aminoglutethimide (975)Aminoglutethimidum (975)Amiodarone hydrochloride (977)Amiodaroni hydrochloridum (977)Amisulpride (978)Amisulpridum (978)Amitriptyline hydrochloride (980)Amitriptylini hydrochloridum (980)Amlodipine besilate (981)Amlodipini besilas (981)Ammonia(13N)injection (817)Ammoniae(13N)solutio iniectabilis (817)Ammoniae solutio concentrata.............................................983Ammonia solution,concentrated. (983)Ammonii bromidum (985)Ammonii chloridum (986)Ammonii glycyrrhizas....................................................5.1-2876 Ammonii hydrogenocarbonas.. (988)Ammonio methacrylate copolymer(type A) (983)Ammonio methacrylate copolymer(type B) (984)Ammonio methacrylatis copolymerum A (983)Ammonio methacrylatis copolymerum B (984)Ammonium(2.4.1.) (103)Ammonium bromide (985)Ammonium chloride (986)Ammonium glycyrrhizate................................................5.1-2876 Ammonium hydrogen carbonate.. (988)Amobarbital (988)Amobarbital sodium (989)Amobarbitalum (988)Amobarbitalum natricum (989)Amoxicillin sodium (990)Amoxicillin trihydrate......................................................5.3-3440 Amoxicillinum natricum (990)Amoxicillinum trihydricum...........................................5.3-3440 Amperometric titration(2.2.19.).. (34)Amphotericin B (995)Amphotericinum B (995)Ampicillin,anhydrous (996)Ampicillin sodium (998)Ampicillin trihydrate (1001)Ampicillinum anhydricum (996)Ampicillinum natricum (998)Ampicillinum trihydricum (1001)Amygdalae oleum raffinatum.......................................5.4-3893 Amygdalae oleum virginale..........................................5.3-3437 Amylum pregelificatum (2490)Anaesthetic ether (1549)Analysis,thermal(2.2.34.) (52)Analytical sieving,particle-size distribution estimation by (2.9.38.).............................................................................5.3-3368 Angelicae radix (1003)Angelica root (1003)Anhydrous silica,hydrophobic colloidal......................5.5-4297 Animal anti-T lymphocyte immunoglobulin for human use (1010)Animal spongiform encephalopathies,products with risk of transmitting agents of (577)Animal spongiform encephalopathy agents,minimising the risk of transmitting via human and veterinary medicinal products(5.2.8.) (463)Aniseed (1006)Anise oil (1004)Anisi aetheroleum (1004)Anisidine value(2.5.36.) (142)Anisi fructus (1006)Anisi stellati aetheroleum (2488)Anisi stellati fructus.........................................................5.5-4297 Antazoline hydrochloride. (1006)Antazolini hydrochloridum (1006)Anthrax spore vaccine(live)for veterinary use (715)Anti-A and anti-B haemagglutinins(indirect method)(2.6.20.) (174)Antibiotics,microbiological assay of(2.7.2.) (188)Anticoagulant and preservative solutions for human blood (1007)Anticomplementary activity of immunoglobulin(2.6.17.)..170 Anticorpora monoclonalia ad usum humanum......5.2-3127 Anti-D antibodies in human immunoglobulins for intravenous administration,test for(2.6.26.)..................................5.3-3348 Anti-D immunoglobulin,human. (1732)Anti-D immunoglobulin,human,assay of(2.7.13.) (205)。
关爱帕金森演讲稿三分钟
大家好！今天，我非常荣幸站在这里，与大家共同探讨一个备受关注的话题——关爱帕金森。
帕金森病是一种常见的神经系统退行性疾病，严重影响患者的生活质量。
在这个特殊的日子里，让我们共同关注帕金森患者，传递关爱，为他们的健康保驾护航。
首先，让我们了解一下帕金森病的现状。
帕金森病是一种慢性进行性疾病，主要影响中老年人，患病率随年龄增长而增加。
据统计，我国帕金森病患者已超过300万人，每年新增患者近10万人。
然而，由于公众对帕金森病的认知不足，许多患者未能得到及时诊断和治疗，导致病情恶化，生活质量下降。
关爱帕金森，首先要提高公众对帕金森病的认知。
帕金森病的症状主要包括震颤、僵硬、运动迟缓、姿势平衡障碍等。
这些症状在早期可能不明显，容易被误诊或忽视。
因此，我们需要加强帕金森病知识的普及，提高公众对帕金森病的认识，使患者能够及时就医，得到有效治疗。
其次，关爱帕金森，需要关注患者的心理健康。
帕金森病患者在疾病早期可能会出现焦虑、抑郁等心理问题。
这是因为疾病给他们带来了生活上的不便和痛苦。
作为关爱帕金森的一员，我们要关注患者的心理健康，给予他们关爱和支持，帮助他们树立战胜疾病的信心。
此外，关爱帕金森，还需要为患者提供便捷的医疗服务。
帕金森病患者需要长期的治疗和康复，这就要求医疗机构提高服务质量，优化诊疗流程，为患者提供便捷、高效的医疗服务。
同时，我们还要关注患者的家庭负担，为患者提供必要的经济援助，减轻他们的生活压力。
为了更好地关爱帕金森患者，我们可以从以下几个方面入手：1. 加强帕金森病知识的普及。
通过举办讲座、发放宣传资料等形式，提高公众对帕金森病的认识，使患者能够及时就医。
2. 建立帕金森病关爱团队。
邀请医护人员、志愿者等组成关爱团队，为患者提供心理、生活、康复等方面的支持。
3. 开展康复训练。
针对帕金森病患者的症状，开展针对性的康复训练，提高他们的生活质量。
4. 加强政策支持。
呼吁政府加大对帕金森病研究的投入，完善相关政策，为患者提供更多的福利。
周日组广播稿-把耳朵唤醒第九期-刘娴琳
把耳朵唤醒第九期（2012第一期）（背景：all is coming to an end）Hello everyone~久违了一个寒假，耳朵我又回来了！这么久没见，大家想我没~！欢迎收听2012年度第一期《把耳朵唤醒》刚刚听到的是来自豆瓣音乐人阿肆的《all is coming to an end》。
大家还记得上学期耳朵放过的那首《我在人民广场吃炸鸡》嘛？这可是阿肆的代表作欧~小编特别喜欢阿肆的声音，还有卖萌的鼻音。
哈哈哈。
听众朋友们如果对她感兴趣的话，可以上阿肆的豆瓣主页听听其他作品~都很不错的说~（背景音乐）沉寂了一年多的山下智久，终于在上个月末发行了新单曲《爱、テキサス》。
作为Yamashita桑所主演的木九剧《最完美的人生终点》的主题曲，此张单曲自然备受关注。
疯狂的女饭们又有耳福了！下面就来听一听这首《爱、テキサス》来自山下智久。
111Music来自山下智久《爱、テキサス》不知道大家有没有听说过樱桃帮呢。
樱桃帮是来自台湾的女子摇滚乐队，以鲜艳的樱桃红作为标志色调。
近日，樱桃帮主唱查查跨队组了一个全新的TEAM，叫做原子邦妮。
下面就来抢先听一下原子邦妮的新作《人鱼》。
小编可是超喜欢主唱MM的声音呢~来自原子邦妮《人鱼》最近不知怎么的，身边的好几个朋友经历了情感波折。
或是沉浸在悲伤中无法自拔，或是心痛后悔抓狂完全变了一个人。
有时候，我们更需要学会的是，如何放手。
这一首蔡健雅的《LETTING GO》，送给仍徘徊在情伤中的痴男怨女们。
MUSIC对于向过去say goodbye和对未来说hello，蔡健雅似乎就是唱感情的高手，不卑不亢，过去的疼痛当然疼，但Tanya会用这疼痛提醒你进化成更好的人。
两年的感情会变淡，淡到若是碰到他，可以用旁观者的身份跳脱出来，这样子亦是一种成长。
慢慢学会放手，看云淡风轻，一个人孤身走我路又如何，留给自己的即是豁然开朗。
MUSIC来自蔡健雅《LETTING GO》广播台本学期新推出点歌版块。
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GYENNO（臻络科技）宣传片
他们,一群“与时间赛跑的人”。
他们,曾经多才多艺，生活多姿多彩；
他们,家庭的顶梁柱；
他们,各自领域的佼佼者。
某一个寻常的清晨，成了人生的转折点。
帕金森，瞬间将他们推入无边的黑暗与痛苦中。
帕金森，作为中老年人常见的中枢神经系统变性疾病，已经成为继肿瘤、心脑血管病之后中老年人的“第三大杀手”。
全球帕金森病患者约450万人，中国约220万人，且每年新发病例近10万人。
多维度的运动障碍导致患者日常生活出现各种功能性障碍问题，肌肉强直，运动迟缓，静止性震颤，姿势步态异常……生活不能自理，生存质量严重下降，患者尊严受损，引发各种心理问题，家庭也倍受拖累。
帕金森病两百年前已被发现，但医学界仍然不明确这种疾病的病因和机制，存在大量的学术空白，目前除了效果有限的药物和手术治疗外，缺乏完整的解决方案以及良好的医疗体验。
GYENNO（臻络科技），有温度的市场导向学术驱动型高科技公司，致力于以科技帮助弱势人群提升生活品质，推进神经病学领域学术发展，构建基于机器人及人工智能技术的立体医疗系统，让每一位所需之人都有机会重塑身体机能。
GYENNO（臻络科技）凭借强大的专家团队卓越的技术力量，紧跟前沿科技，自主研发新型设备，搭建医疗服务平台，联合传统药企、医疗器械企业和专家学者共同为帕金森患者提供立体化、信息化完整解决方案，提高患者生活品质，提升患者治疗体验。
目前，公司成功开发“医动力”、“睿云”两套云系统和睿餐智能防抖勺、步态辅助仪两大产品。
“睿餐”智能防抖勺具有360度全方位防抖效果，可有效抵消85%以上的手部抖动，让原本不能正常进食的手抖人群进食无忧。
步态辅助仪对患者进行准确有效的感官刺激，以辅助患者克服步态症状，恢复正常行走能力。
两大产品从“手”到“脚”，从“形”到“形而上”，为帕金森病患者提供完整的“运动障碍立体解决方案”。
医动力是一款针对帕金森及运动障碍人群的慢病管理软件，能实现监测、干预、研究的远程闭环医疗体系。
通过绑定睿餐防抖勺、步态辅助仪等硬件设备，实现对患者运动症状数据的精准量化采集；
患者自主选择私人医生，私人医生可依据采集的数据及用药记录对病情进行动态监测并分析药物预后效果与病情发展，完成对患者的健康管理。
睿云-帕金森数据分析系统，基于“中国帕金森病及运动障碍疾病临床大数据库建设专家共识”，涵盖多维度临床数据录入及管理、智能查询及统计、数据分析及数据挖掘、科研课题及多中心管理等主要功能，针对不同的临床及科研需求，为医、药及学术界提供全方位的数据管理及分析服务，共同推进帕金森领域的学术发展。
让残缺的生命绽放光彩，GYENNO（臻络科技）。