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Implications of Diagnostic Delay in Duchenne Muscular Dystrophy
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Recognising & Preventing Duchenne Muscular Dystrophy
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Facioscapulohumeral Dystrophy Associated with Hearing Loss & Coats Syndrome
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A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
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Telemedicine in Neurology
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Duchenne Muscular Dystrophy
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Mechanisms, Causes, and Effects of Hypercapnia
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Palliative Care and Neurology
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LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
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Case 35-2006: A Newborn Boy with Hypotonia
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Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
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Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
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Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
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Hypoglycaemia in Spinal Muscular Atrophy
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Facioscapulohumeral Muscular Dystrophy in Early Childhood
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Congenital Muscular Dystrophy
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Practical Problems in the Respiratory Care of Patients with Muscular Dystrophy
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Facioscapulohumeral Dystrophy Presenting in Infancy with Facial Diplegia & Sensorineural Deafness
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Myotonic Dystrophy
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Abnormal Iris Vasculature in Myotonic Dystrophy
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