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Showing articles 0 to 15 of 15 Filter Applied: molecular genetics (Click to remove) The Autosomal Recessive Cerebellar Ataxias NEJM 366:636-646, Anheim,M.,et al, 2012 Fragile X Premutation With Atypical Symptoms at Onset Arch Neurol 63:1135-1138, Cellini,E.,et al, 2006 Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects Lancet Neurol 4:239-248, Shahwan, A., et al, 2005 Molecular Basis of the Neurodegenerative Disorders NEJM 340:1970-1980, Martin,J.B., 1999 Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts Neurol 48:482-485, Zhou,Y.X.,et al, 1997 Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan) Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997 Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997 The Inherited Ataxias and the New Genetics JNNP 61:327-332, Hammans,S.R., 1996 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995 Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus J Med Genet 32:25-31, Twist,E.C.,et al, 1995 Trinucleotide Repeat Length and Rate of Progression of Huntington's Disease Ann Neurol 36:630-635, Illarioshkin,S.N.,et al, 1994 Trinucleotide Repeat Expansion in Neurological Disease Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994 Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging Arch Neurol 50:803-806, Klockgether,T.,et al, 1993 Molecular Genetics in Neurology Ann Neurol 34:757-773, Martin,J.B., 1993 Showing articles 0 to 15 of 15