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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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Palliative Care and Neurology
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A 52-year-old Woman with Progressive Proximal Weakness
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The Ever-Expanding Spectrum of Congenital Muscular Dystrophies
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Cancer Risk Among Patients with Myotonic Muscular Dystrophy
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Gene Therapy for Duchenne Muscular Dystrophy: Expectations and Challenges
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Congenital Muscular Dystrophy
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Diagnostic Evaluation of Clinically Normal Subjects with Chronic hyperCKemia
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Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
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The Phenotype of Limb-Girdle Muscular Dystrophy Type 21
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Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
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Mutations in the Sarcoglycan Genes in Patients with Myopathy
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Investigation of Muscle Disease
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The Heart in Myotonic Dystrophy
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Autosomal Recessive Distal Dystrophy
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Molecular Genetics of Duchenne and Becker Muscular Dystrophy
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DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
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Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
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