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Showing articles 0 to 13 of 13 Filter Applied: genetic testing (Click to remove) A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025 The Spectrum of Fragile X Disorders NEJM 393:281-288, Hagerman,R.H. & Hagerman,P.J., 2025 A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia Neurol 105:e213993, Shen,F.,et al, 2025 Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia Neurol 105:e214099, Mizutani,H.,et al, 2025 A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency Neurol 100:206-212, Stamm,B.,et al, 2023 A 28-Year-Old Woman with Vision Loss and an Unusual Gait Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021 A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness Neurol 94:994-999, Wildman, J.,et al, 2020 Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019 FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018 Huntington Disease: Clinical Features and Diagnosis UptoDate Dec 2017, Oksana Suchowersky, 2017 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population J Pediatr 129:611-614, Giangreco,C.A.,et al, 1996 Advances in Molecular Analysis of Fragile X Syndrome 552, Warren,W.T.&Nelson,D.L.JAMA 271:536-553, 1994 Showing articles 0 to 13 of 13