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Showing articles 0 to 6 of 6 Filter Applied: trinucleotide repeats (Click to remove) A 48-Year-Old Man With Spasticity and Progressive Ataxia Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023 Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis UptoDate 2022 Jan, Darras, B.T., 2022 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 and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,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 Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy Arch Neurol 52:25-31, Ricker,K.,et al, 1995 Showing articles 0 to 6 of 6