Table of Contents

Pathology and Diagnosis of Muscular Dystrophies.- Standards of Care for Duchenne Muscular Dystrophy: Brief Treat-NMD Recommendations.- Genetics and Pathogenesis of Distal Muscular Dystrophies.- Phenotype Variations in Early Onset Pompe Disease: Diagnosis and Treatment Results with Myozyme®.- Diseases of the Human Mihondrial Oxidative Phosphorylation System.- Mihondrial Diseases: A Cross-Talk Between Mihondrial and Nuclear Genomes.- Mihondrial Disorders Due to Nuclear OXPHOS Gene Defects.- Coenzyme Q10 Deficiencies in Neuromuscular Diseases.- The Role of Mihondrial Network Dynamics in the Pathogenesis of Charcot-Marie-Tooth Disease.- Pathogenesis and Treatment of Mihondrial Disorders.- Biology of Peripheral Inherited Neuropathies: Schwann Cell Axonal Interactions.- Phenotype and Clinical Evolution of Charcot-Marie-Tooth Disease Type 1A Duplication.- Genotypes & Sensory Phenotypes in 2 New X-Linked Neuropathies (CMTX3 and dSMAX) and Dominant CMT/HMN Overlap Syndromes.- Natural History and Treatment of Peripheral Inherited Neuropathies.- Spinal Muscular Atrophy During Human Development: Where Are the Early Pathogenic Findings?.- Spinal Muscular Atrophy.- Friedreich Ataxia: An Update on Animal Models, Frataxin Function and Therapies.- Genetics and Pathogenesis of Inherited Ataxias and Spastic Paraplegias.