Titlebook: Inherited Neuromuscular Diseases; Translation from Pat Carmen Espinós,Vicente Felipo,Francesc Palau Book 2009 The Editor(s) (if applicable)

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書目名稱Inherited Neuromuscular Diseases影響因子(影響力)




書目名稱Inherited Neuromuscular Diseases影響因子(影響力)學(xué)科排名




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書目名稱Inherited Neuromuscular Diseases網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Inherited Neuromuscular Diseases被引頻次




書目名稱Inherited Neuromuscular Diseases被引頻次學(xué)科排名




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書目名稱Inherited Neuromuscular Diseases讀者反饋學(xué)科排名

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Advances in Experimental Medicine and Biologyhttp://image.papertrans.cn/i/image/466465.jpg

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978-94-007-3056-4The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature B.V. 200

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Standards of Care for Duchenne Muscular Dystrophy: Brief Treat-NMD Recommendations,d on the generation of brief standards of care for DMD, which are presented here and are available via the TREAT-NMD website (.). Guidelines are presented for diagnostics, neurological follow up, gastrointestinal and nutritional issues, respiratory and cardiac care as well as orthopaedics, rehabilitation, psychosocial interventions and oral care.

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Phenotype and Clinical Evolution of Charcot-Marie-Tooth Disease Type 1A Duplication,d early childhood; (iii) proximal lower-limb musculature involvement as a late phenotypic feature; and (iv) minimal adult phenotype. We also briefly revise genetic, electrophysiological, pathological and neuroimaging data of the disease.

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Pathology and Diagnosis of Muscular Dystrophies,approach, necessary to conduct genetic studies and to offer an appropriate genetic counseling. The application of molecular medicine in genetic muscular dystrophies also brings great expectations to the therapeutic management of these patients.