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

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Standards of Care for Duchenne Muscular Dystrophy: Brief Treat-NMD Recommendations,improve outcomes in DMD but these are not uniformly applied. This leads to inequality in access to treatment, as well as problems for planning controlled trials of future therapeutics. A worldwide effort is underway to generate care guidelines for DMD, which involves the Centre for Disease Control i

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,Phenotype Variations in Early Onset Pompe Disease: Diagnosis and Treatment Results with Myozyme?,cogen accumulation in the lysosomes, leading to lysosomal swelling, cellular damage and organ dysfunction. Patient age at the onset of Pompe disease symptoms and the rate of deterioration can vary considerably..In early onset patients (the classical infantile form) this glycogen accumulation leads t

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Coenzyme Q10 Deficiencies in Neuromuscular Diseases,ransition pore and uncoupling proteins. Furthermore, this compound is a specific substrate for enzymes of the fatty acids β–oxidation pathway and pyrimidine nucleotide biosynthesis. Furthermore, CoQ is an antioxidant that acts in all cellular membranes and lipoproteins. A complex of at least ten nuc

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The Role of Mitochondrial Network Dynamics in the Pathogenesis of Charcot-Marie-Tooth Disease,ary defect of either the mtDNA or nuclear genome encoded subunits of the respiratory chain. These organelles have also been directly involved in the pathogenesis of Mendelian neurodegenerative disorders caused by mutations in nuclear-encoded proteins targeted to mitochondria, such as Friedreich atax

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Pathogenesis and Treatment of Mitochondrial Disorders,efects of the mitochondrial respiratory chain (RC), has made great strides. Mitochondrial diseases can be due to mutations in mitochondrial DNA (mtDNA) or in nuclear DNA (nDNA) and each group can be subdivided into more specific classes. Thus, mtDNA-related disorders can result from mutations in gen

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