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Showing articles 0 to 12 of 12 Filter Applied: muscular dystrophy (Click to remove) Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996 Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988 Diseases of Muscles-Clinical Manifestations & Differential Diagnosis The New Physic 263, 1967, Oct., Boshes,L., 1967 Mechanisms, Causes, and Effects of Hypercapnia UptoDate Dec, Feller-Kopman, D.J. & Schwartzstein, R.M., 2016 Diagnostic Evaluation of Clinically Normal Subjects with Chronic hyperCKemia Neurol 66:1585-1587, Fernandez,C.,et al, 2006 The Prevention of Neurogenetic Disease Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995 Hypoglycaemia in Spinal Muscular Atrophy Lancet 346:609-610, Bruce,A.K.,et al, 1995 Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992 DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis Hum Genet 82:55-58, Defesche,J.C.,et al, 1989 Inflammatory Facioscapulohumeral Muscular Dystrophy & Coats Syndrome Ann Neurol 12:398-401, Wulff,J.D.,et al, 1982 Quadriceps Myopathy-Entity or Syndrome Arch Neurol 31:60, Boddie,H.,et al, 1974 Neuro CPC of MGH Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958 Showing articles 0 to 12 of 12