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Showing articles 0 to 14 of 14 Filter Applied: genetic testing (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 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 Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy JAMA Neurol 81:83-84, Hua,L.,et al, 2024 Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023 A 48-Year-Old Man With Spasticity and Progressive Ataxia Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023 Spinal Muscular Atrophy UpToDate, Oct, Bodamer,O.A., 2022 Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement AJNR 40:903-907, Hartin, I.,et al, 2019 Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism NEJM 372:1151-1162, Miller, B.L.,et al, 2015 Non-Alzheimers Dementia 1 Frontotemporal Dementia Lancet 386:1672-1682, Bang, Jee.,et al, 2015 Showing articles 0 to 14 of 14