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

Showing articles 0 to 9 of 9 Filter Applied: gene mutation (Click to remove) Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease NEJM 360:1729-1739, Hara,K.,et al, 2009 Alexander Disease, Ventricular Garlands and Abnormalities of the Medulla and Spinal Cord Neurol 66:494-498,468, van der Knaap,M.S.,et al, 2006 Unusual Variants of Alexander's Disease Ann Neurol 57:327-338, van der Knaap,M.S., et al, 2005 Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997 Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker NEJM 328:471-475, Shelbourne,P.,et al, 1993 Molecular Genetics in Neurology Ann Neurol 34:757-773, Martin,J.B., 1993 Neurodegeneration with Brain Iron Accumulation AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019 Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019 Genetic Aspects of Alzheimer Disease The Neurologist 15:80-86, Williamson,J.,et al, 2009 Showing articles 0 to 9 of 9