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Showing articles 0 to 9 of 9 Filter Applied: gene (Click to remove) A Hereditary Moyamoya Syndrome With Multisystemic Manifestations Neurol 75:259-264, Herv�,D., et al, 2010 New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy JNNP 81:946-953, Klinge,L.,et al, 2010 Amyotrophic Lateral Sclerosis Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007 Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene Brain 129:1674-1684, Horvath, R.,et al, 2006 Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope BMJ 326:1078-1079, Plunkett,A.,et al, 2003 Clinical and Genetic Aspects of Distal Myopathies Muscle Nerve 24:1440-1450, Saperstein,D.S.,et al, 2001 Distal Myopathies:Clinical and Molecular Diagnosis and Classification JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999 A Novel Mutation in Exon 3 of the Proteolipid Protein Gene in Pelizaeus-Merzabacher Disease Neurol 45:394-395, Pratt,V.M.,et al, 1995 Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy Neurol 41:823-828, Olney,R.K.,et al, 1991 Showing articles 0 to 9 of 9