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Showing articles 0 to 12 of 12 Filter Applied: molecular genetics (Click to remove) The Autosomal Recessive Cerebellar Ataxias NEJM 366:636-646, Anheim,M.,et al, 2012 Diagnosis and New Treatment in Muscle Channelopathies JNNP 80:360-365, Meola,G.,et al, 2009 Fragile X Premutation With Atypical Symptoms at Onset Arch Neurol 63:1135-1138, Cellini,E.,et al, 2006 Distal Myopathies:Clinical and Molecular Diagnosis and Classification JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999 Misdiagnosis Revealed by Genetic Linkage Analysis in a Family with Wilson Disease Neurol 46:1485-1486, Vidaud,D.,et al, 1996 Myotonic Dystrophy In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994 The Nondystrophic Myotonias In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,R.,et al, 1994 Wilson Disease Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992 Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism NEJM 327:57, Cossu,P.,et al, 1992 Clinicopath Conf Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992 Homing in on Wilson's Disease Editorial, Lancet 1:822-8231989., , 1989 McArdle's Disease:Biochemical and Molecular Genetic Studies Ann Neurol 24:774-781, Servidei,S.,et al, 1988 Showing articles 0 to 12 of 12