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Showing articles 0 to 12 of 12 Filter Applied: familial (Click to remove) Fatal Avian Influenza A (H5N1) in a Child Presenting with Diarrhea Followed by Coma NEJM 352:686-691, de Jong,M.D., et al, 2005 Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis UptoDate 2022 Jan, Darras, B.T., 2022 Recurrent Cerebral Ischemia During Pregnancies Neurol 95:e2453-e2457, Bulwa, Z.,et al, 2020 Red Papules on the Tongue of a Patient with Hemiparesis JAMA 312:741-742, Chiu, H.Y. & Lin, S.J., 2014 An unusual cause of stroke and hypoxia BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011 Presence of Diarrhea and Absence of Tendon Xanthomas in Patients With Cerebrotendinous Xanthomatosis Arch Neurol 57:520-524, Verrips,A.,et al, 2000 Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation JNNP 69: 5-12, Gray,R.G.F. et al, 2000 Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy Arch Neurol 52:25-31, Ricker,K.,et al, 1995 Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases Neurol 45:1405-1408, Heckmann,J.M.,et al, 1995 Liver Transplantation as a Treatment for Familial Amyloidotic Polyneuropathy Ann Int Med 120:133-134, Skinner,M.,et al, 1994 A Disorder of Azonal Development, Necrotizing Myopathy, Cardiomyopathy, and Cataracts:A New Familial Disease Ann Neurol 27:193-199, Lyon,G.,et al, 1990 Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features Arch Neurol 45:1118-1122, Uitti,R.J.,et al, 1988 Showing articles 0 to 12 of 12