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3. Inborn errors of metabolism in children referred with Reye's syndrome. A changing pattern. Rowe PC; Valle D; Brusilow SW JAMA; 1988 Dec; 260(21):3167-70. PubMed ID: 3184395 [TBL] [Abstract][Full Text] [Related]
4. 3-Methylglutaconyl-CoA hydratase, 3-methylcrotonyl-CoA carboxylase and 3-hydroxy-3-methylglutaryl-CoA lyase deficiencies: a coupled enzyme assay useful for their detection. Narisawa K; Gibson KM; Sweetman L; Nyhan WL Clin Chim Acta; 1989 Sep; 184(1):57-64. PubMed ID: 2480857 [TBL] [Abstract][Full Text] [Related]
5. Progress in Reye syndrome: epidemiology, biochemical mechanisms and animal models. Kilpatrick-Smith L; Hale DE; Douglas SD Dig Dis; 1989; 7(3):135-46. PubMed ID: 2659225 [No Abstract] [Full Text] [Related]
11. Isolated biotin-resistant deficiency of 3-methylcrotonyl-CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcome. Bannwart C; Wermuth B; Baumgartner R; Suormala T; Weismann UN J Inherit Metab Dis; 1992; 15(6):863-8. PubMed ID: 1293382 [TBL] [Abstract][Full Text] [Related]
12. A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiency. Wilson WG; Cass MB; Søvik O; Gibson KM; Sweetman L Eur J Pediatr; 1984 Sep; 142(4):289-91. PubMed ID: 6489380 [TBL] [Abstract][Full Text] [Related]
13. Propionyl-CoA carboxylase deficiency in a patient with biotin-responsive 3-methylcrotonylglycinuria. Sweetman L; Bates SP; Hull D; Nyhan WL Pediatr Res; 1977 Nov; 11(11):1144-7. PubMed ID: 917614 [TBL] [Abstract][Full Text] [Related]
14. Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency in two sibs. Beemer FA; Bartlett K; Duran M; Ghneim HK; Wadman SK; Bruinvis L; Ketting D Eur J Pediatr; 1982 Jul; 138(4):351-4. PubMed ID: 7128647 [TBL] [Abstract][Full Text] [Related]
15. The measurement of propionyl-CoA carboxylase and pyruvate carboxylase activity in hair roots: its use in the diagnosis of inherited biotin-dependent enzyme deficiencies. Wolf B; Raetz H Clin Chim Acta; 1983 May; 130(1):25-30. PubMed ID: 6851181 [TBL] [Abstract][Full Text] [Related]
16. A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria. Bartlett K; Ng H; Leonard JV Clin Chim Acta; 1980 Jan; 100(2):183-6. PubMed ID: 6766095 [TBL] [Abstract][Full Text] [Related]