Mitochondrial DNA and Disease
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Neurosarcoidosis:Signs, Course and Treatment in 35 Confirmed Cases
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Acromegaly
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Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
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Alcohol and Alcoholism
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Diagnosis and New Treatments in Muscular Dystrophies
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Mitochondrial DNA Polymerase-y and Human Disease
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Mitochondrial Respiratory-Chain Diseases
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Cerebral Infarction Associated with Kearns-Sayre Syndrome-Related Cardiomyopathy
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991
Friedreich Ataxia
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Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
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Central Core Disease, Clinical Features in 13 Patients
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Cytochrome c Oxidase Deficiency in Leigh Syndrome
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Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
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