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Titlebook: Clinical Handbook of Neuromuscular Medicine; David Walk Book 20181st edition Springer International Publishing AG, part of Springer Nature

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发表于 2025-3-21 16:17:30 | 显示全部楼层 |阅读模式
书目名称Clinical Handbook of Neuromuscular Medicine
编辑David Walk
视频video
概述A concise and practical overview of neuromuscular diseases for residents, trainees and fellows.Provides an understanding for diagnostic techniques and patient management strategies.Fulfills a gap in t
图书封面Titlebook: Clinical Handbook of Neuromuscular Medicine;  David Walk Book 20181st edition Springer International Publishing AG, part of Springer Nature
描述.This concise and practical book provides an overview of neuromuscular disorders in clinical practice. Diagnostic approaches are covered along with patient management strategies in an easy-to-understand and introductory framework.  Filling a significant gap in the literature, this resource delivers essential information for neurology trainees and practitioners, as well as anyone interested in learning the fundamentals of this important medical subspecialty..
出版日期Book 20181st edition
关键词neuromuscular diseases; neuromuscular transmission; anterior horn cell disorders; respiratory managemen
版次1
doihttps://doi.org/10.1007/978-3-319-67116-1
isbn_softcover978-3-030-09791-2
isbn_ebook978-3-319-67116-1
copyrightSpringer International Publishing AG, part of Springer Nature 2018
The information of publication is updating

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发表于 2025-3-21 22:04:48 | 显示全部楼层
Diseases of Muscle,rns of muscle weakness on exam can narrow the differential diagnosis. Serum creatine kinase, focused serologic testing, electromyography, exercise test, muscle imaging, biopsy, and genetic testing are useful to reach a specific diagnosis. The key clinical features, laboratory, EMG, and histopatholog
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Motor Neuron Disorders,flexia, atrophy, and weakness. SMA is the most common childhood-onset motor neuron disorder and is an autosomal recessive disorder of the SMN gene. Other less common motor neuron disorders include SBMA, PLS, Hirayama disease, and viral poliomyelitis. The differential diagnosis and management of moto
发表于 2025-3-22 10:11:02 | 显示全部楼层
Diseases of Nerve,ician. Once identified, these clinical deficits can be further characterized by their pattern of involvement and temporal evolution. Taken together, these elements of the history and physical can help the clinician create a neuropathy differential diagnosis that targets the most likely etiologies. A
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The Diagnostic Approach to the Hypotonic and Weak Infant,agnosis challenging. A systematic diagnostic approach is important to localization, beginning with distinguishing between central and peripheral causes of hypotonia. This chapter describes how to apply the clinical evaluation and ancillary testing including electrodiagnostic, biochemical, and geneti
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Electrodiagnostic Testing,vous system. Latency, amplitude, duration, and conduction velocity on nerve conduction studies help assess the integrity of motor and sensory nerves. Needle EMG analysis of spontaneous activity, MUAP morphology, and MUAP recruitment provide more specific information on potential neuropathic or myopa
发表于 2025-3-23 03:04:54 | 显示全部楼层
Ventilatory Management in Neuromuscular Disease, failure and proper treatment can extend duration of life and improve quality of life. Treatment modalities include noninvasive ventilation, invasive ventilation with tracheostomy, and airway clearance therapy with aggressive treatment of acute respiratory infections.
发表于 2025-3-23 09:22:35 | 显示全部楼层
Genetic Testing in Neuromuscular Disease,of the appropriate use, limitations, and utility of testing options. Recognition of common patterns of inheritance and exceptions to these patterns may help in identifying appropriate tests. In addition, an understanding of the common types of mutations in specific diseases and the methodologies emp
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