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Showing articles 0 to 13 of 13 Filter Applied: trinucleotide repeats (Click to remove) Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022 Few Psychological Consequences of Presymptomatic Testing for Huntington Disease Lancet 349:4, Bundey,S., 1997 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 Clinical Genetics in Neurological Disease JNNP 57:7-15, MacMillan,J.C.&Harper,P.S., 1994 A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats NEJM 330:1401-1406, 14501994., Kremer,B.,et al, 1994 Myotonic Dystrophy In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994 Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test JAMA 270:1569-1575, Brown,W.,et al, 1993 Persistent Respiratory Failure Following Cardiac Arrest Neurol 90:e2174-e2178, Fullam, T. & Sladky, J.H., 2018 A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes Ann Neurol 77:1-7, Scripko, P.,et al, 2015 Clinical Features and Neuropathology of Autosomal Dominant Spinocerebellar Ataxia (SCA17) Ann Neurol 43:367-375, Rolfs,A.,et al, 2003 CAG Repeat Number Governs the Development Rate of Pathology in Huntington's Disease Ann Neurol 41:689-692, Penney,J.B.,et al, 1997 Relationship Between Trinucleotide Repeats and Neuropathological Changes in Huntington's Disease Ann Neurol 39:132-136, Furtado,S.,et al, 1996 Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp Neurol 45:24-30, Genis,D.,et al, 1995 Showing articles 0 to 13 of 13