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Titlebook: Neuromuscular Disorders; A Comprehensive Revi Satish V. Khadilkar,Rakhil S. Yadav,Bhagyadhan A. Book 20181st edition Springer Nature Singa

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发表于 2025-3-21 19:50:17 | 显示全部楼层 |阅读模式
书目名称Neuromuscular Disorders
副标题A Comprehensive Revi
编辑Satish V. Khadilkar,Rakhil S. Yadav,Bhagyadhan A.
视频video
概述A case based learning of neuromuscular disorders.Description of key differential clinical points.Analysis of investigation in clinical context.Guidance for genetic tests.Comprehensive management guide
图书封面Titlebook: Neuromuscular Disorders; A Comprehensive Revi Satish V. Khadilkar,Rakhil S. Yadav,Bhagyadhan A.  Book 20181st edition Springer Nature Singa
描述.This book provides a concise overview of the diagnosis and therapy of a wide variety of neuromuscular disorders, in tabulated form and with illustrative cases..Treating neuromuscular disorders calls for a sound, step-by-step clinical approach based on differential diagnosis and laboratory investigations. Yet to date, there has been no single, compact book that offers all the relevant information related to the management of these disorders.. .This book fills that gap, presenting the state of the art in the field and addressing practical problems together with their solutions. Each chapter covers disorder characteristics, clinical differentiating points, relevant investigations and their interpretation, available genetic testing, best management approaches and counselling. Illustrative cases provide valuable insights, while extensive tables and illustrations mean that information can be rapidly found..
出版日期Book 20181st edition
关键词Anterior horn cell disease; Neuropathy; Myasthenia gravis; Myopathy; Practical approach
版次1
doihttps://doi.org/10.1007/978-981-10-5361-0
isbn_softcover978-981-13-5377-2
isbn_ebook978-981-10-5361-0
copyrightSpringer Nature Singapore Pte Ltd. 2018
The information of publication is updating

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Motor Neuron Diseases (Amyotrophic Lateral Sclerosis)xed; and can have different combinations of upper and lower motor neuron findings. These are usually sporadic in nature, while some forms can be familial. Amyotrophic lateral sclerosis (ALS) is common and active disorder of brain and spinal cord motor neurons. ALS is fundamentally a clinical diagnos
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Acute Motor Axonal Neuropathyajor subtype of GBS. AMAN progresses more rapidly and has an earlier peak than demyelinating GBS; tendon reflexes are relatively preserved or even exaggerated, and autonomic dysfunction is rare. Molecular mimicry of human gangliosides by . lipo-oligosaccharides is believed to be the main pathophysio
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Post-polio Syndromeg over other areas. The involvement is restricted to the lower motor neuron. The condition needs to be differentiated from other causes of lower motor neuron diseases, and background of poliomyelitis is perhaps most important. While new cases of polio are not encountered in the modern times, individ
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