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Showing articles 0 to 12 of 12 Filter Applied: trinucleotide repeats (Click to remove) Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis UptoDate 2022 Jan, Darras, B.T., 2022 A 48-Year-Old Man With Spasticity and Progressive Ataxia Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023 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 Brugada Syndrome in Spinal and Bulbar Muscular Atrophy Neurol 82:1813-1821, Araki, A.,et al, 2014 Degenerative Diseases of the Nervous System, Friedreich Ataxia Adams & Victors Principles of Neurology, Chp 39, pg 1102, Ropper, A.H.,et al, 2014 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy Arch Neurol 52:25-31, Ricker,K.,et al, 1995 Cardiac Involvement in a Large Kindred with Myotonic Dystrophy:Quant Assess & Relation to Size of CTG Repeat Expansion JAMA 274:813-819, Tokgozoglu,L.S.,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 Molecular Genetics in Neurology Ann Neurol 34:757-773, Martin,J.B., 1993 The Polymerase Chain Reaction:Application to Nervous System Disease Ann Neurol 34:513-523, Darnell,R.B., 1993 Showing articles 0 to 12 of 12