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Showing articles 0 to 8 of 8 Filter Applied: gene mutation (Click to remove) MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study AJNR 29:1638-1643, Fulbright,R.K.,et al, 2008 Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease NEJM 386;674-687, Case 5-2022, 2022 Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease Neurol 92:101-103, Kang, M.J.,et al, 2019 Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3 NEJM 377:2376-2385, Case 38-2017, 2017 MRI Findings of Biotin-Responsive Basal Ganglia Disease Before and After Treatment Neurol 86:e71-e72, Saeedan, M.B. & Dogar, M.A., 2016 A 27-Year Old Man with Rapidly Progressive Coma Neurol 85:e74-e78, Wong,J.M.,et al, 2015 Sturge-Weber Syndrome UptoDate , Nov, Bodensteiner, J.B., 2014 Sturge-Weber Syndrome MedLink Neurology, July, Comi, A.M., 2013 Showing articles 0 to 8 of 8