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

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書目名稱Clinical Handbook of Neuromuscular Medicine影響因子(影響力)




書目名稱Clinical Handbook of Neuromuscular Medicine影響因子(影響力)學科排名




書目名稱Clinical Handbook of Neuromuscular Medicine網(wǎng)絡(luò)公開度




書目名稱Clinical Handbook of Neuromuscular Medicine網(wǎng)絡(luò)公開度學科排名




書目名稱Clinical Handbook of Neuromuscular Medicine被引頻次




書目名稱Clinical Handbook of Neuromuscular Medicine被引頻次學科排名




書目名稱Clinical Handbook of Neuromuscular Medicine年度引用




書目名稱Clinical Handbook of Neuromuscular Medicine年度引用學科排名




書目名稱Clinical Handbook of Neuromuscular Medicine讀者反饋




書目名稱Clinical Handbook of Neuromuscular Medicine讀者反饋學科排名

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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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慌張

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

露天歷史劇

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

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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.

千篇一律

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