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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Palliative Care in Neurology
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Pure Motor Hand Weakness
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Prenatal Diagnosis of Duchenne Muscular Dystrophy Using a Single Fetal Nucleated Erythrocyte in Maternal Blood
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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The Prevention of Neurogenetic Disease
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Deficiency of Brain Synaptic Dystrophin in Human Duchenne Muscular Dystrophy
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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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Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
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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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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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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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Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
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Trinucleotide Repeat Expansion in Neurological Disease
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Facioscapulohumeral Muscular Dystrophy in Early Childhood
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Myotonic Dystrophy with No Trinucleotide Repeat Expansion
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Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
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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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Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
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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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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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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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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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Skeletal Muscle Toxoplasmosis in Patients with Acquired Immunodeficiency Syndrome:A Clinicopath Study
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Dystrophinopathy in Isolated Cases of Myopathy in Females
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Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
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Oculomotor, Auditory, and Vestib ular Responses in Myotonic Dystrophy
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