Advances in chemical diagnosis and treatment of metabolic disorders

Partial table of contents: LACTIC ACIDEMIA. Biochemical Defects in Pyruvate Dehydrogenase Complex Deficiency (Y. Kuroda, et al.). Urinary Organic Acid Profiles of Melas Patients with Complex 1 Deficiency (Y. Kusunoki, et al.). ORGANIC ACIDEMIA. Multiple Carboxylase Deficiency: A Case Report (H. Chikaoka, et al.). The ''Unspecified Syndrome'' Type of 3-Methylglutaconic Aciduria (H. Tanaka, et al.). UREA CYCLE DISORDER. Mass Spectrometry in the Diagnosis and Treatment of Ornithine Transcarbamylase Deficiency in Two Brothers (S. Murao). DRUG-INDUCED METABOLIC DEFECT. Metabolic Changes in a Case of Acute Encephalopathy Associated with Administration of Calcium Hopantenate (M. Kajita, et al.). ANALYTICAL TECHNIQUES. High-Performance Liquid Chromatographic Determination of Urinary Acylcarnitine (T. Shinka, et al.). Indexes.