A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
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Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy
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New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
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Diagnosis and Etiology of Congenital Muscular Dystrophy
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Case 35-2006: A Newborn Boy with Hypotonia
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Mutations in the Sarcoglycan Genes in Patients with Myopathy
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Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
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Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
Neurol 46:461-465, North,K.N.,et al, 1996
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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Deficiency of Brain Synaptic Dystrophin in Human Duchenne Muscular Dystrophy
Ann Neurol 38:446-449, Kim,T.W.,et al, 1995
Brain Abnormalities in Duchenne Muscular Dystrophy:Phosphorus-31 Magnetic Resonance Spectroscopy & Neuropsych Study
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Myotonic Dystrophy
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Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
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Recognising & Preventing Duchenne Muscular Dystrophy
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Diagnostic Delay in Duchenne's Muscular Dystrophy
JAMA 247:478-480, Crisp,D.E.,et al, 1982
Mental Deficiency Associated with Muscular Dystrophy
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