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Showing articles 0 to 5 of 5 Filter Applied: multiple sclerosis,differential diagnosis of (Click to remove) Plasma R Binder Deficiency & Neurologic Disease NEJM 317:1330-1332, Sigal,S.H.,et al, 1987 Hereditary Defect of Cobalamin Metabolism (cblG Mutation) Presenting as a Neurologic Disorder in Adulthood NEJM 318:1738-1741, 1752-17541988., Carmel,R.,et al, 1988 Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) NEJM 360:1656-1665, Case 12-2009, 2009 Neurological Manifestations of Fabry Disease in Female Carriers Ann Neurol 4:537-540, Bird,T.D.,et al, 1978 Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem Neurol 23:1030, Sipe,J.C., 1973 Showing articles 0 to 5 of 5