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Showing articles 0 to 11 of 11 Filter Applied: metabolic disorder,primary (Click to remove) Neonatal Seizures NEJM 388:1692-1700, Ropper.A.H., 2023 Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency NEJM 375:1879-1890, Case 34-2016, 2016 MRI Characteristics of Globus Pallidus Infarcts in Isolated Methylmalonic Acidemia AJNR 36:194-201, Baker, E.H.,et al, 2015 Cerebrospinal Fluid Analysis in the Workup of GLUT1 Deficiency Syndrome JAMA Neurol 70:1440-1444, Leen, W.G.,et al, 2013 Practice Parameter: Evaluation of the Child with Global Developmental Delay Neurol 60:367-380, Shevell,M.,et al, 2003 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 Conditions That Mimic Stroke in the Emergency Department Arch Neurol 52:1119-1122, Libman,R.B.,et al, 1995 Cardioembolic Stroke in Primary Oxalosis with Cardiac Involvement DiPasquale. G. , et al, Stroke 20:1403-14069., , 1989 Cerebellar Hemorrhage Complication Methylmalonic & Propionic Acidemia Arch Neurol 41:1293-1296, Dave,P.,et al, 1984 Angiokeratoma Corporis Diffusum Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962 Showing articles 0 to 11 of 11