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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Serial MRI in Fukuyama Type Congenital Muscular Dystrophy
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Ventricular Late Potentials in Myotonic Dystrophy
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Hearing Loss in Facioscapulohumeral Muscular Dystrophy
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Autosomal Recessive Distal Dystrophy
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Welander's Distal Myopathy:Clinical Neurophysiol & Muscle Biopsy Obser in Young & Middle Aged Adults with Early Symptoms
JNNP 54:494-498, Borg,K., 1991
Prednisone in Duchenne Dystrophy, A Randomized, Controlled Trial Defining the Time Course & Dose Response
Arch Neurol 48:383-388, Griggs,R.C.,et al, 1991
Mononuclear Cell Analysis of Muscle Biopsies in Prednisone-Treated & Untreated Duchenne Muscular Dystrophy
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A Comparison of Daily and Alternate-Day Prednisone Therapy in the Treatment of Duchenne Muscular Dystrophy
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Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function
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Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
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Long-Term Benefit from Prednisone Therapy in Duchenne Muscular Dystrophy
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Myotonic Heart Disease:A Clinical Follow-Up
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The Effect of Spine Fusion on Respiratory Function in Duchenne Muscular Dystrophy
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Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
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Graves Orbitopathy:Correlation of CT and Clinical Findings
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Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudo-Obstruction:POLIP Syndrome
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Attitudes of Mothers to Neonatal Screening for Duchenne Muscular Dystrophy
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Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990
Location of Facioscapulohumeral Muscular Dystrophy Gene on Chromosome 4
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Adult Phosphorylase b Kinase Deficiency
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Night-Time Nasal Ventilation in Neuromuscular Disease
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Magnetic Resonance Imaging and Clinical Correlates of Intellectual Impairment in Myotonic Dystrophy
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Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
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Criteria for Establishing the Validity of Genetic Recombination in Myotonic Dystrophy
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Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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Gastric Hypomotility in Duchenne's Muscular Dystrophy
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Peripheral Neuropathy in Myotonic Dystrophy:A Nerve Biopsy Study
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Hydrops and Pleural Effusions in Congenital Myotonic Dystrophy
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Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
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Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
Lancet 2:425-427, Greenberg,C.R.,et al, 1988
Effect of Chronic Treatment with the Calcium Antagonist Diltiazem in Duchenne Muscular Dystrophy
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Hearing Loss in Myotonic Dystrophy
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Central Nervous System Magnetic Resonance Imaging Findings in Myotonic Dystrophy
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Life Spans of Duchenne Muscular Dystrophy Patients in the Hospital Care Program in Japan
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