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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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Mitochondrial DNA and Disease
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Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
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Hypoglycaemia in Spinal Muscular Atrophy
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Evaluation of the Cardiomyopathy in Becker Muscular Dystrophy
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The Prevention of Neurogenetic Disease
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Myoblast Transfer in the Tratment of Duchenne's Muscular Dystrophy
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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Facioscapulohumeral Muscular Dystrophy in Early Childhood
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Trinucleotide Repeat Expansion in Neurological Disease
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Cardiomyopathy May Be the Only Clinical Manifestation in Female Carriers of Duchenne Muscular Dystrophy
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Sudden Death of a Carrier of X-Linked Emery-Dreifuss Muscular Dystrophy
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Molecular Genetics in Neurology
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The Polymerase Chain Reaction:Application to Nervous System Disease
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Analysis of Dystrophin Expression after Activation of Myogenesis in Amniocytes, Chorionic-Villus Cells, and Fibroblasts
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Duchenne Muscular Dystrophy:Deficiency of Dystrophin-Associated Proteins in the Sarcolemma
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Gene Therapy for Duchenne Dystrophy
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Myoblast Transfer in Duchenne Muscular Dystrophy
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Cerebral Abnormalities in Myotonic Dystrophy
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Ophthalmologic Manifestations in MELAS Syndrome
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Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
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Experience with Screening Newborns for Duchenne Muscular Dystrophy in Wales
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Duchenne Dystrophy:Randomized, Controlled Trial of Prednisone (18 months) & Azathioprine (12 months)
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Cyclosporine Increases Muscular Force Generation in Duchenne Muscular Dystrophy
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Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker
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Brief Report:Reverse Mutation in Myotonic Dystrophy
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Genetics and Physiology of the Myotonic Muscle Disorders
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Abnormal Expression of Dystrophin-Associated Proteins in Fukuyama-Type Congenital Muscular Dystrophy
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Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
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Upper Gastrointestinal Tract Motility in Children with Progressive Muscular Dystrophy
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Dystrophinopathy in Isolated Cases of Myopathy in Females
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Detection of Duchenne and Becker MD Carriers by Quant Multiplex Polymerase Chain Reaction
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Diagnosis of Duchenne & Becker Muscular Dystrophies by Polymerase Chain Reaction
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Oculomotor, Auditory, and Vestib ular Responses in Myotonic Dystrophy
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Unstable DNA Sequence in Myotonic Dystrophy
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Phenotypic Expression of the Myotonic Dystrophy Gene in Monozygotic Twins
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The Heart in Myotonic Dystrophy
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Fasioscapulohumeral and Scapuloperoneal Syndromes
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