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Showing articles 0 to 8 of 8 Filter Applied: genetic screening (Click to remove) The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale Stroke 43:2871-2876, Pescini, F.,et al, 2012 Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019 Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability NEJM 367:1921-1929, Ligt, J.,et al, 2012 Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome) UpToDate, Feb, Shovlin, C., 2011 Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts & Leukoencephalopathy (CADASIL) UpToDate (www.uptodate.com) Aug 21, Dichgans,M.,et al., 2007 Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997 Clinical Spectrum of CADASIL:A Study of 7 Families Lancet 346:934-939, Chabriat,H.,et al, 1995 Screening for von Hippel-Lindau Disease by DNA Polymorphism Analysis JAMA 267:1226-1231, Glenn,G.M.,et al, 1992 Showing articles 0 to 8 of 8