96 related articles for article (PubMed ID: 4454060)
1. Coexistence of defective activity in glycine-cleavage reaction and propionyl-CoA carboxylase in the liver of a hyperglycinemic child.
Nishimura Y; Tada K; Arakawa T
Tohoku J Exp Med; 1974 Jul; 113(3):267-71. PubMed ID: 4454060
[No Abstract] [Full Text] [Related]
2. 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
[TBL] [Abstract][Full Text] [Related]
3. Propionyl coenzyme A carboxylase deficiency presenting as non-ketotic hyperglycinaemia.
Harris DJ; Thompson RM; Wolf B; Yang BI
J Med Genet; 1981 Apr; 18(2):156-7. PubMed ID: 7241536
[TBL] [Abstract][Full Text] [Related]
4. Propionic acidaemia presenting with pancytopaenia in infancy.
Sweetman L; Nyhan WL; Cravens J; Zomer Y; Plunket DC
J Inherit Metab Dis; 1980; 2(3):65-9. PubMed ID: 6796762
[TBL] [Abstract][Full Text] [Related]
5. Identification of the insertion/deletion mutation in Spanish beta-propionyl-CoA carboxylase-deficient patients.
Pérez-Cerdá C; Rodríguez-Pombo P; Ugarte M
J Inherit Metab Dis; 1994; 17(6):661-3. PubMed ID: 7707688
[No Abstract] [Full Text] [Related]
6. Stimulation of propionyl CoA and beta-methylcrotonyl CoA carboxylase activities in human leukocytes and cultured fibroblasts by biotin.
Wolf B; Rosenberg LE
Pediatr Res; 1979 Nov; 13(11):1275-9. PubMed ID: 514693
[No Abstract] [Full Text] [Related]
7. Dipropylacetate and propionyl CoA carboxylase.
Wolf B
Lancet; 1978 Aug; 2(8085):369. PubMed ID: 79729
[No Abstract] [Full Text] [Related]
8. Biotin-dependent carboxylase deficiencies (propionyl-CoA and pyruvate carboxylases).
Gravel RA; Robinson BH
Ann N Y Acad Sci; 1985; 447():225-34. PubMed ID: 3925855
[No Abstract] [Full Text] [Related]
9. Propionic acidemia with severe hyperammonemia and defective glycine metabolism.
Shafai T; Sweetman L; Weyler W; Goodman SI; Fennessey PV; Nyhan WL
J Pediatr; 1978 Jan; 92(1):84-6. PubMed ID: 619088
[No Abstract] [Full Text] [Related]
10. Asymptomatic propionyl CoA carboxylase deficiency in a 13-year-old girl.
Wolf B; Paulsen EP; Hsia YE
J Pediatr; 1979 Oct; 95(4):563-5. PubMed ID: 480035
[No Abstract] [Full Text] [Related]
11. 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]
12. 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
[TBL] [Abstract][Full Text] [Related]
13. Leukocyte propionyl-CoA carboxylase deficiency in a patient with ketotic hyperglycinaemia.
Del Valle JA; Merinero B; Garciá MJ; Ugarte M; Omeñaca F; Neustadt G
J Inherit Metab Dis; 1980; 3(3):93. PubMed ID: 6775147
[No Abstract] [Full Text] [Related]
14. Heterozygote expression in propionyl coenzyme A carboxylase deficiency. Differences between major complementation groups.
Wolf B; Rosenberg LE
J Clin Invest; 1978 Nov; 62(5):931-6. PubMed ID: 711858
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Prenatal diagnosis and family studies in a case of propionicacidaemia.
Gompertz D; Goodey PA; Thom H; Russell G; Johnston AW; Mellor DH; MacLean MW; Ferguson-Smith ME; Ferguson-Smith MA
Clin Genet; 1975 Oct; 8(4):244-50. PubMed ID: 1183068
[TBL] [Abstract][Full Text] [Related]
17. Living-related liver transplantation for neonatal-onset propionic acidemia.
Yorifuji T; Muroi J; Uematsu A; Nakahata T; Egawa H; Tanaka K
J Pediatr; 2000 Oct; 137(4):572-4. PubMed ID: 11035841
[TBL] [Abstract][Full Text] [Related]
18. [Propionic acidemia: report of a case that is successfully managed by peritoneal dialysis and sodium benzoate therapy].
Hsu WC; Lin SP; Huang FY; Wang PA; Hsiao KJ
Zhonghua Yi Xue Za Zhi (Taipei); 1990 Nov; 46(5):306-10. PubMed ID: 2178070
[TBL] [Abstract][Full Text] [Related]
19. L-carnitine therapy in propionicacidaemia.
Roe CR; Bohan TP
Lancet; 1982 Jun; 1(8286):1411-2. PubMed ID: 6123699
[No Abstract] [Full Text] [Related]
20. Propionic acidemia--biochemical studies.
Barash V; Elpeleg O; Amit R; Gottfried S; Yatziv S; Gutman A
Isr J Med Sci; 1989 Feb; 25(2):103-6. PubMed ID: 2495260
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]