Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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A 30-year-old Man with Progressive Weakness and Atrophy
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The Limbic-Girdle Muscular Dystrophies
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Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
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LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
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Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
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Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
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Muscular Dystrophies
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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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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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Transition to Adult Care for Children with Chronic Neurological Disorders
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Diagnosis and Etiology of Congenital 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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New Strategy for Prenatal Diagnosis of X-Linked Disorders
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Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic 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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Obstetric Aspects in Women with FSH Muscular Dystrophy, Limb-Girdle Musc Dyst, & Cogen Myopathies
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Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
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Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
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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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Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
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Facioscapulohumeral Muscular Dystrophy in Early Childhood
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Abnormal Expression of Dystrophin-Associated Proteins in Fukuyama-Type Congenital Muscular Dystrophy
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The Polymerase Chain Reaction:Application to Nervous System Disease
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Serial MRI in Fukuyama Type Congenital Muscular Dystrophy
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Night-Time Nasal Ventilation in Neuromuscular Disease
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Congenital Muscular Dystrophy
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Peripheral Neuropathy in Myotonic Dystrophy:A Nerve Biopsy Study
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Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
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Facioscapulohumeral Dystrophy Associated with Hearing Loss & Coats Syndrome
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Clinical Symposia, Scoliosis
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