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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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Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
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Facioscapulohumeral Muscular Dystrophy in Early Childhood
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Peripheral Nerve Injury and Causalgia Secondary to Routine Venipuncture
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Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
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Rapid Direct Diagnosis of Deletions Carriers of Duchenne and Becker Muscular Dystrophies
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The Shoulder-Hand Syndrome after Stroke:A Prospective Clinical Trial
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Post-Traumatic Movement Disorders:Central and Peripheral Mechanisms
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Trinucleotide Repeat Expansion in Neurological Disease
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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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Signs and Symptoms of Reflex Sympathetic Dystrophy:Prospective Study of 829 Patients
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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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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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Acquired Ocular Visual Impairment in Children, 1960-1989
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Abnormal Expression of Dystrophin-Associated Proteins in Fukuyama-Type Congenital Muscular Dystrophy
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Diag of Occult Muscular Dystrophy:"Chance"Finding of Elevated Serum Aminotransferase Act
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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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Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
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Upper Gastrointestinal Tract Motility in Children with Progressive Muscular Dystrophy
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Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
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The Use of Magnetic Resonance Imaging in Diagnosing Infantile Neuroaxonal Dystrophy
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Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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