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OhuraTKobayashiKAbukawaDTazawaYAikawaJSakamotoOet alA novel inborn error of metabolism detected by elevated methionine and/or galactose in newborn screening: neonatal intrahepatic cholestasis caused by citrin deficiency

Disorders of Branched-Chain Amino Acid Metabolism Details of the various diseases resulting from mutations in the enzymes of branched-chain amino acid catabolism are presented in the Branched-Chain Amino Acid Metabolism Disorders page as well as in specific pages for individual diseases, for example Maple Syrup Urine Disease, MSUD

Risk of health status worsening in primary infertile men: A prospective 10-year follow-up study

a c , ATP depletion with sodium arsenate (Ars