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Showing articles 0 to 8 of 8 Filter Applied: genetic screening (Click to remove) 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 Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019 The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale Stroke 43:2871-2876, Pescini, F.,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 Adrenoleukodystrophy JAMA 294:3131-3134, Moser,H.W.,et al, 2005 Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations Neurol 47:1269-1277, Baser,M.E., 1996 Showing articles 0 to 8 of 8