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Inherited Neuromuscular Diseases

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Cover of 'Inherited Neuromuscular Diseases'

Table of Contents

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    Book Overview
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    Chapter 1 Pathology and Diagnosis of Muscular Dystrophies
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    Chapter 2 Standards of Care for Duchenne Muscular Dystrophy: Brief Treat-NMD Recommendations
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    Chapter 3 Genetics and Pathogenesis of Distal Muscular Dystrophies
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    Chapter 4 Phenotype Variations in Early Onset Pompe Disease: Diagnosis and Treatment Results with Myozyme®
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    Chapter 5 Inherited Neuromuscular Diseases
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    Chapter 6 Mitochondrial Diseases: A Cross-Talk Between Mitochondrial and Nuclear Genomes
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    Chapter 7 Mitochondrial Disorders Due to Nuclear OXPHOS Gene Defects
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    Chapter 8 Coenzyme Q10 Deficiencies in Neuromuscular Diseases
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    Chapter 9 The Role of Mitochondrial Network Dynamics in the Pathogenesis of Charcot-Marie-Tooth Disease
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    Chapter 10 Pathogenesis and Treatment of Mitochondrial Disorders
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    Chapter 11 Biology of Peripheral Inherited Neuropathies: Schwann Cell Axonal Interactions
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    Chapter 12 Phenotype and Clinical Evolution of Charcot-Marie-Tooth Disease Type 1A Duplication
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    Chapter 13 Genotypes & sensory phenotypes in 2 new X-linked neuropathies (CMTX3 and dSMAX) and dominant CMT/HMN overlap syndromes.
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    Chapter 14 Natural History and Treatment of Peripheral Inherited Neuropathies
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    Chapter 15 Spinal Muscular Atrophy During Human Development: Where Are the Early Pathogenic Findings?
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    Chapter 16 Spinal Muscular Atrophy
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    Chapter 17 Friedreich Ataxia: An Update on Animal Models, Frataxin Function and Therapies
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    Chapter 18 Genetics and Pathogenesis of Inherited Ataxias and Spastic Paraplegias
Attention for Chapter 17: Friedreich Ataxia: An Update on Animal Models, Frataxin Function and Therapies
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