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Showing articles 0 to 14 of 14 Filter Applied: genetic neurologic disorders (Click to remove) 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 MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study AJNR 29:1638-1643, Fulbright,R.K.,et al, 2008 Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q Neurol 62:87-90, Basel-Vanagaite,L.,et al, 2004 Familial Infantile Bilateral Striatal Necrosis Neurol 59:983-989, Straussberg,R.,et al, 2002 Acute Profound Dystonia in Infants with Glutaric Acidemia Pediatrics 83:228-234, Bergman,I.,et al, 1989 Leigh Disease (Subacute Necrotizing Encephalomyelopathy) :CT & MR in Five Cases J Comput Assist Tomogr 12:40-44, Geyer,C.A.,et al, 1988 Infantile Bilateral Striatal Necrosis, Clinicopathological Classification Arch Neurol 43:677-680, Mito,T.,et al, 1986 Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) NEJM 360:1656-1665, Case 12-2009, 2009 Update on Blepharospasm: Report from the BEBRF International Workshop Neurol 71:1275-1282, Hallett,M.,et al, 2008 Autosomal Dominant Acute Necrotizing Encephalopathy Neurol 61:226-230, Neilson,D.E.,et al, 2003 Multiple Sclerosis NEJM 343:938-952, Noseworthy,J.H. et al, 2000 Clinical Spectrum of CADASIL:A Study of 7 Families Lancet 346:934-939, Chabriat,H.,et al, 1995 Juvenile Parkinsonism Treated with Levodopa Arch Neurol 34:244, Sachdev,K.K.,et al, 1977 Showing articles 0 to 14 of 14