Enter your terms above and click the 'Search' button.

Showing articles 0 to 8 of 8 Filter Applied: gene mutation (Click to remove) A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever Neurol 102:e209358, Barbosa,A.R.,et al, 2024 Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis UptoDate 2022 Jan, Darras, B.T., 2022 Progressive Proximal Weakness in a 56-year-old Man with Bone Pain Neurol 93:939-944, Torabi,T.,et al, 2019 Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation JAMA Neurol 74:114-118, , 2017 Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency NEJM 375:1879-1890, Case 34-2016, 2016 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 A Case of Refractory Nocturnal Seizures Neurol 84:e134-e136, Pavlakis, P.P. & Douglass, L.M., 2015 The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration Arch Neurol 67:161-170,145, Yu,C.-E.,et al, 2010 Showing articles 0 to 8 of 8