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

Showing articles 0 to 12 of 12 Filter Applied: gene (Click to remove) Fibromuscular Dysplasia and Its Neurologic Manifestations JAMA Neurol 76:217-226, Touze, E.,et al, 2019 A Hereditary Moyamoya Syndrome With Multisystemic Manifestations Neurol 75:259-264, Herv�,D., et al, 2010 Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023 Ehlers-Danlos Syndromes BMJ 366:I4966, Ghali, N.,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 The Autosomal Recessive Cerebellar Ataxias NEJM 366:636-646, Anheim,M.,et al, 2012 Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease NEJM 360:1729-1739, Hara,K.,et al, 2009 Autosomal Dominant Moyamoya Disease Maps to Chromosome 17q25.3 Neurol 70:2357-2363, Mineharu,Y.,et al, 2008 Hereditary Hemorrhagic Telangiectasia NEJM 333:918-924, Guttmacher,A.E.,et al, 1995 Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred Medicine 68:1-29, Lamiell,J.M.,et al, 1989 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 Showing articles 0 to 12 of 12