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Showing articles 0 to 8 of 8 Filter Applied: gene (Click to remove) Recurrent Cerebral Ischemia During Pregnancies Neurol 95:e2453-e2457, Bulwa, Z.,et al, 2020 An unusual cause of stroke and hypoxia BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011 Reduced Penetrance,Variable Expressivity,and Genetic Heterogeneity of Familial Atrial Septal Defects Circulation 97:2043-2048, Benson,D.W.,et al, 1998 Degenerative Diseases of the Nervous System, Friedreich Ataxia Adams & Victors Principles of Neurology, Chp 39, pg 1102, Ropper, A.H.,et al, 2014 Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients Medicine 86:1-7, Cottin,V.,et al, 2007 Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope BMJ 326:1078-1079, Plunkett,A.,et al, 2003 Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene NEJM 342:770-780, Dalakas,M.C.,et al, 2000 Hereditary Hemorrhagic Telangiectasia NEJM 333:918-924, Guttmacher,A.E.,et al, 1995 Showing articles 0 to 8 of 8