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Duchenne Muscular Dystrophy
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Accuracy of a Machine Learning Muscle MRI - Based Tool for the Diagnosis of Muscular Dystrophies
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Muscular Dystrophies
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Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
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Persistent Respiratory Failure Following Cardiac Arrest
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Heart Transplantation in a Patient with Myotonic Dystrophy Type 1 and End-Stage Dilated Cardiomyopathy: A Short Term Follow-up
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Mechanisms, Causes, and Effects of Hypercapnia
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A 52-year-old Woman with Progressive Proximal Weakness
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The Limbic-Girdle Muscular Dystrophies
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Electrophysiological Study with Prophylactic Pacing and Survival in Adults with Myotonic Dystrophy and Conduction System Disease
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The Ever-Expanding Spectrum of Congenital Muscular Dystrophies
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Muscle Histology vs MRI in Duchenne Muscular Dystrophy
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Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy
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LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
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Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
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New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
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Diagnosis and New Treatments in Muscular Dystrophies
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A 49-Year-Old Man with Contractures, Weakness, and Cardiac Arrhythmia
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Electrocardiographic Abnormalities and Sudden Death in Myotonic Dystrophy Type 1
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Diagnosis and Etiology of Congenital Muscular Dystrophy
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Cardiac Involvement in Patients With Limb-Girdle Muscular Dystrophy Type 2 and Becker Muscular Dystrophy
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Congenital Muscular Dystrophy
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Case 35-2006: A Newborn Boy with Hypotonia
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Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
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Clinical Relevance of Atrial Fibrillation/Flutter, Stroke, Pacemaker Implant, and Heart Failure in Emery-Dreifuss Muscular Dystrophy
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Clinical and Genetic Aspects of Distal Myopathies
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Cardiac Dysfunction in Neuromuscular Diseases
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Signs and Symptoms of Duchenne Muscular Dystrophny and Becker Muscular Dystrophy Among Carriers in the Netherlands: A Cohort Study
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Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency
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The Muscular Dystrophies
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Cardiac Involvement in Genetically Confirmed Facioscapulohumeral Muscular Dystrophy
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Mutations in the Sarcoglycan Genes in Patients with Myopathy
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Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
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Bent Spine Syndrome
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Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
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Development of Cardiomyopathy in Female Carriers of Duchenne and Becker Muscular Dystrophies
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Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
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Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
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Investigation of Muscle Disease
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The Prevention of Neurogenetic Disease
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Brain Abnormalities in Duchenne Muscular Dystrophy:Phosphorus-31 Magnetic Resonance Spectroscopy & Neuropsych Study
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Cardiac Involvement in a Large Kindred with Myotonic Dystrophy:Quant Assess & Relation to Size of CTG Repeat Expansion
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