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The Prevention of Neurogenetic Disease
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Trinucleotide Repeat Expansion in Neurological Disease
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Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
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Myotonic Dystrophy with No Trinucleotide Repeat Expansion
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Facioscapulohumeral Muscular Dystrophy in Early Childhood
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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 Nondystrophic Myotonias
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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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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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Skeletal Muscle Toxoplasmosis in Patients with Acquired Immunodeficiency Syndrome:A Clinicopath Study
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Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
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ELISA Quantitation of Dystrophin for the Diagnosis of Duchenne and Becker Muscular Dystrophies
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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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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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Fasioscapulohumeral and Scapuloperoneal Syndromes
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Serial MRI in Fukuyama Type Congenital Muscular Dystrophy
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Response to Treatment with Antihistamines in a Family with Myotonia Congenita
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Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
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The Effect of Spine Fusion on Respiratory Function in Duchenne Muscular Dystrophy
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Long-Term Benefit from Prednisone Therapy in 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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Hearing Loss in Facioscapulohumeral Muscular Dystrophy
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