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Showing articles 0 to 13 of 13 Filter Applied: gene mutation (Click to remove) 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 Pes Cavus and Neuropathy Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019 Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019 Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy Neurol 90:e1827-e1831, Xiao, F.,et al, 2018 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 A 35-year-old Woman with Hyperstartling Stiffness, and Accidental Falls Neurol 88:e38-e41, Russo, S.P.,et al, 2017 Leukodystrophy and Progressive Myoclonic Epilepsy Disclosing DRPLA Neurol 86:e58-e59, Sgobbi de Souza, P.V.,et al, 2016 Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014 Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014 GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease Neurol 77:1287-1294, Prust, M.,et al, 2011 Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia Neurol 49:1617-1620, Ragno,M.,et al, 1997 Showing articles 0 to 13 of 13