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Showing articles 0 to 9 of 9 Filter Applied: metabolic disorder,primary-screening tests (Click to remove) Screening for Inherited Metabolic Diseases in Adults with Neurological Disease Lancet 1:1101, Wierzbicki,A.S.,et al, 1988 Inborn Errors of Metabolism Ann Neurol 11:221-232, Kolodny,E.H.,et al, 1982 Pyruvate Dehydrogenase Deficiency (PDCD) eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018 Cerebral Venous Sinus Thrombosis in Homocystinuria: Dietary Intervention in Conjunction with Anticoagulation Sage Open Med Case Reports 5:1-4, Yap, S.,et al, 2017 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, Maple Syrup Urine Disease Adams & Victors Principles of Neurology, Chp 37, pg 953, Ropper, A.H.,et al, 2014 Inherited Metabolic Diseases of the Nervous System, The Phenylketonuria Adams & Victors Principles of Neurology, Chp 37, pg 968, Ropper, A.H.,et al, 2014 Practice Parameter: Evaluation of the Child with Global Developmental Delay Neurol 60:367-380, Shevell,M.,et al, 2003 Clinical Findings in Four Children with Biotinidase Deficiency Detected Through a Statewide Neonatal Screening Program NEJM 313:16-19, 43-441985., Wolf,B.,et al, 1985 Showing articles 0 to 9 of 9