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Showing articles 0 to 13 of 13 Filter Applied: gene mutation (Click to remove) Melas Syndrome Stat PearlsPubl Jan 25, Pia,S. & Lui,F., 2025 A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles Neurol 103:e209796, Bouchart,J.,et al, 2024 Characyeristic features and progression of abnormalities on MRI for CARASIL Neurol 85:459-463, Sekine, Y., etal, 2015 Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2 NEJM 370:911-920, Zhou, Q.,et al, 2014 Degenerative Diseases of the Nervous System, Alzheimer Disease Adams & Victors Principles of Neurology, Chp 39, pg 1063, Ropper, A.H.,et al, 2014 A Prematurely Aging Patient Presenting with Severe Leukoaraiosis and Stroke Neurol 78:e113-e114, Seixas,J.C.,et al, 2012 Clinical Spectrum of CADASIL and the Effect of Cardiovascular Risk Factors on Phenotype: Study in 200 Consecutively Recruited Individuals Stroke 41:630-634, Adib-Samii,P., et al, 2010 Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease NEJM 360:1729-1739, Hara,K.,et al, 2009 Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) NEJM 360:1656-1665, Case 12-2009, 2009 Role of COL4A1 in Small-Vessel Disease and Hemorrhagic Stroke NEJM 354:1489-1496, Gould,D.B.,et al, 2006 Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) Pract Neurology 4:50-55, Razvi,S.S.M. &Muir,K.W., 2004 De Novo Mutation in the Notch3 Gene Causing CADASIL Ann Neurol 47:388-391, Joutel,A.,et al, 2000 Distribution of Cranial MRI Abnormalities in Patients with Symptomatic and Subclinical CADASIL BJR 73:256-265, Coulthard, A.,et al, 2000 Showing articles 0 to 13 of 13