Enter your terms above and click the 'Search' button.

Showing articles 0 to 8 of 8 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 28-Year-Old Woman with Vision Loss and an Unusual Gait Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021 Persistent Respiratory Failure Following Cardiac Arrest Neurol 90:e2174-e2178, Fullam, T. & Sladky, J.H., 2018 Huntington Disease: Clinical Features and Diagnosis UptoDate Dec 2017, Oksana Suchowersky, 2017 Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997 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 Myotonic Dystrophy In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994 Showing articles 0 to 8 of 8