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Showing articles 0 to 12 of 12 Filter Applied: familial (Click to remove) Inherited Metabolic Diseases of the Nervous System, Hepatolenticular Degeneration (Wilson Disease) Adams & Victors Principles of Neurology, Chp 37, pg 982, Ropper, A.H.,et al, 2014 Middle Cerebral Artery Main Stem Thrombosis in Two Siblings with Familial Thrombotic Thrombocytopenic Purpura Neurol 50:1157-1160, Kelly,P.J.,et al, 1998 Cerebromeningeal Haemophagocytic Lymphohistiocytosis Lancet 239:104-107, Henter,J.&Elinder,G., 1992 Erythromelalgia:Review of Clinical Characteristics and Pathophysiology Am J Med 91:416-422, Jurzrock,R.&Cohen,P.R., 1991 Mendelian Etiologies of Stroke Ann Neurol 22:175-192, Natowicz,M.&Kelley,R.I., 1987 A 14-Year-Old Girl with Headache, Seizures, and Confusion Neurol 92:e161-e167, Xiao, L.,et al, 2019 FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018 Neuromyelitis Optica Spectrum Disorders UpToDate, May, Glisson,C.C., 2016 Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2 NEJM 370:911-920, Zhou, Q.,et al, 2014 An unusual cause of stroke and hypoxia BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011 Aicardi-Gouti�res Syndrome Br Med Bull 89:183-201, Orcesi, S.,et al, 2009 Recurrent Meningitis in a Patient with Congenital Deficiency of the C9 Component of Complement Arch Int Med 150:2395-2399, Zoppi,M.,et al, 1990 Showing articles 0 to 12 of 12