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Showing articles 0 to 11 of 11 Filter Applied: metabolic disorder,primary (Click to remove) Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency NEJM 375:1879-1890, Case 34-2016, 2016 Neonatal Seizures NEJM 388:1692-1700, Ropper.A.H., 2023 Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 Inherited Metabolic Diseases of the Nervous System, Pyridoxine Dependent Seizures Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,et al, 2014 Inherited Metabolic Diseases of the Nervous System, Biopterine Deficiency Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,et al, 2014 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 Neonatal Epileptic Encephalopathy Lancet 361:1614, Clayton,P.T.,et al, 2003 Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998 NEJM 339:1914-1923, , 1998 Prenatal Genetic Diagnosis NEJM 283:1370, Milunsky,A.,et al, 1970 Screening for Inborn Errors of Metabolism Associated with Mental Deficiency or Neurologic Disorders or Both NEJM 274:384, Renuart,A., 1966 Showing articles 0 to 11 of 11