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Showing articles 0 to 15 of 15 Filter Applied: gene mutation (Click to remove) Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man Neurol 88:e26-e29, Qin, C.,et al, 2017 Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease NEJM 360:1729-1739, Hara,K.,et al, 2009 Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome NEJM 385:1317-1325, Case 30-2021, 2021 A Teenager with Persistent Headache Neurol 92:e1526-e1531, Hu, Y.,et al, 2019 Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018 The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification Neurol 87:e56-e57, Saini, A.G.,et al, 2016 Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency NEJM 375:1879-1890, Case 34-2016, 2016 Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use Neurol 84:e165-e169, Whitlock, J.B.,et al, 2015 A Prematurely Aging Patient Presenting with Severe Leukoaraiosis and Stroke Neurol 78:e113-e114, Seixas,J.C.,et al, 2012 MELAS MedLink.com, August, Klopstock, T., 2012 LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine Disease Models & Mechanisms 4:562-568, Lu,J.T., et al, 2011 Prothombotic Mutations as Risk Factors for Cryptogenic Ischemic Cerebrovascular Events in Young Subjects With Patent Foramen Ovale Stroke 38:2070-2073, Botto,N.,et al, 2007 A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review The Neurologist 8:302-312, Thambisetty,M.,et al, 2002 Fits and Strokes Lancet 358:120, Sharma,P.,et al, 2001 De Novo Mutation in the Notch3 Gene Causing CADASIL Ann Neurol 47:388-391, Joutel,A.,et al, 2000 Showing articles 0 to 15 of 15