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Showing articles 0 to 12 of 12 Filter Applied: CAG repeats (Click to remove) The Spectrum of Fragile X Disorders NEJM 393:281-288, Hagerman,R.H. & Hagerman,P.J., 2025 Family History and DNA Analysis in Patients With Suspected Huntington's Disease JNNP 69:54-59, Siesling,S. et al, 2000 Patients with Features Similar to Huntington's Disease, Without CAG Expansion in Huntingtin Neurol 51:215-220, Rosenblatt,A.,et al, 1998 Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families Neurol 51:1666-1671, Moseley,M.L.,et al, 1998 Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS Neurol 49:568-572, Parboosingh,J.S.,et al, 1997 Genetic Testing of Children at Risk for Huntington's Disease Neurol 49:1048-1053, Nance,M.A.,et al, 1997 Diagnosis of Patients Presenting to a Huntington Disease (HD) Clinic without a Family History of HD Neurol 47:1578-1580, Nance,M.A.,et al, 1996 Mutation Analysis in Patients with Possible but Apparently Sporadic Huntington's Disease Lancet 344:714-717, Davis,M.B.,et al, 1994 Trinucleotide Repeat Expansion in Neurological Disease Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994 A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes Ann Neurol 77:1-7, Scripko, P.,et al, 2015 iH NMR Spectroscopy Studies of Huntington's Disease, Correlations with CAG Repeat Numbers Neurol 50:1357-1365, Jenkins,B.G.,et al, 1998 The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997 Showing articles 0 to 12 of 12