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Showing articles 0 to 11 of 11 Filter Applied: metabolic disorder,primary (Click to remove) 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 Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998 NEJM 339:1914-1923, , 1998 Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem Neurol 23:1030, Sipe,J.C., 1973 Neonatal Seizures NEJM 388:1692-1700, Ropper.A.H., 2023 Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 Cerebrospinal Fluid Analysis in the Workup of GLUT1 Deficiency Syndrome JAMA Neurol 70:1440-1444, Leen, W.G.,et al, 2013 Acute Intermittent Porphyria Presenting as Acute Pancreatitis and Posterior Reversible Encephalopathy Syndrome Acta Neurol Taiwan 17:177-183, Shen, F.,et al, 2008 Neonatal Epileptic Encephalopathy Lancet 361:1614, Clayton,P.T.,et al, 2003 Diagnostic Yield of the Neurologic Assessment of the Developmentally Delayed Child J Pediatr 127:193-199, Majnemer,A.&Shevell,M.I., 1995 Conditions That Mimic Stroke in the Emergency Department Arch Neurol 52:1119-1122, Libman,R.B.,et al, 1995 Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin NEJM 304:817-820, Thoene,J.,et al, 1981 Showing articles 0 to 11 of 11