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Showing articles 0 to 11 of 11 Filter Applied: familial (Click to remove) A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia Neurol 105:e213993, Shen,F.,et al, 2025 A 28-Year-Old Woman with Vision Loss and an Unusual Gait Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021 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 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes Ann Neurol 77:1-7, Scripko, P.,et al, 2015 Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014 Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family Neurol 45:325-331, Fink,J.K.,et al, 1995 X-Linked Pure Familial Spastic Paraparesis Arch Neurol 52:665-669, Cambi,F.,et al, 1995 Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis Neurol 41:174-181, Nygaard,T.G.,et al, 1991 Hallervorden-Spatz Syndrome and Brain Iron Metabolism Arch Neurol 48:1285-1293, Swaiman,K.F., 1991 Showing articles 0 to 11 of 11