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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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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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Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
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Clinicopathologic Conference, Systemic Immunoglobulin Light-Chain (AL) Amyloidosis
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Molecular and Neurological Features of MELAS Syndrome in Paediatric Patients: A Case Series and Review of the Literature
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Hearing and Vision Loss in an Older Man
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Alcohol and Alcoholism
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LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
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Mitochondrial DNA Polymerase-y and Human Disease
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Mitochondrial Respiratory-Chain Diseases
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Mitochondrial DNA and Disease
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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A Clinical Study of Noonan Syndrome
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Ischemic Cerebrovascular Complications and Risk Factors in Idiopathic Hypertrophic Subaortic Stenosis
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The Effects of Alcoholism on Skeletal and Cardiac Muscle
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Friedreich Ataxia
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Chloroquine Neuromyotoxicity, Clinical & Pathological Perspective
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Cytochrome c Oxidase Deficiency in Leigh Syndrome
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Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
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Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
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