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2. [Biotin deficiency in the germ-free rat and propionic acidemia]. Cherruau B, Sacquet E, Mangeot M, Demelier JF, Lemonnier A. Ann Nutr Metab; 1983; 27(1):48-56. PubMed ID: 6830142 [Abstract] [Full Text] [Related]
3. Differential effects of biotin deficiency and replenishment on rat liver pyruvate and propionyl-CoA carboxylases and on their mRNAs. Rodríguez-Meléndez R, Pérez-Andrade ME, Díaz A, Deolarte A, Camacho-Arroyo I, Cicerón I, Ibarra I, Velázquez A. Mol Genet Metab; 1999 Jan; 66(1):16-23. PubMed ID: 9973543 [Abstract] [Full Text] [Related]
6. Lymphocyte propionyl-CoA carboxylase is an early and sensitive indicator of biotin deficiency in rats, but urinary excretion of 3-hydroxypropionic acid is not. Mock DM, Mock NI. J Nutr; 2002 Jul; 132(7):1945-50. PubMed ID: 12097674 [Abstract] [Full Text] [Related]
7. Effect of valine on propionate metabolism in control and hyperglycinemic fibroblasts and in rat liver. Revsin B, Lebowitz J, Morrow G. Pediatr Res; 1977 Jun; 11(6):749-53. PubMed ID: 17092 [Abstract] [Full Text] [Related]
8. Abnormal metabolites of isoleucine in a patient with propionyl-CoA carboxylase deficiency. Sweetman L, Weyler W, Nyhan WL, de Céspedes C, Loria AR, Estrada Y. Biomed Mass Spectrom; 1978 Mar; 5(3):198-207. PubMed ID: 630060 [Abstract] [Full Text] [Related]
13. Dietary treatment and biochemical studies on a neonatal case of propionyl-CoA carboxylase deficiency. DelValle JA, Merinero B, Jiménez A, García MJ, Ugarte M, Omeñaca F, Neustadt G, Quero J. J Inherit Metab Dis; 1982 Apr; 5(2):121-4. PubMed ID: 6820422 [Abstract] [Full Text] [Related]
16. The identification of (E)-2-methylglutaconic acid, a new isoleucine metabolite, in the urine of patients with beta-ketothiolase deficiency, propionic acidaemia and methylmalonic acidaemia. Duran M, Bruinvis L, Ketting D, Kamerling JP, Wadman SK, Schutgens RB. Biomed Mass Spectrom; 1982 Jan; 9(1):1-5. PubMed ID: 7059658 [Abstract] [Full Text] [Related]
17. Propionic acidaemia. First case in the Finnish population. von Wendt L, Similä S, Ruostesuo J, Puukka M, Ruokonen A. Ann Clin Res; 1983 Jan; 15(5-6):194-6. PubMed ID: 6667016 [Abstract] [Full Text] [Related]
19. Coding sequence mutations in the alpha subunit of propionyl-CoA carboxylase in patients with propionic acidemia. Campeau E, Dupuis L, León-Del-Rio A, Gravel R. Mol Genet Metab; 1999 May; 67(1):11-22. PubMed ID: 10329019 [Abstract] [Full Text] [Related]