These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
111 related articles for article (PubMed ID: 4430155)
1. Detection of inborn errors of metabolism. II. Defects in propionic acid metabolism. Hill HZ; Goodman SI Clin Genet; 1974; 6(2):73-8. PubMed ID: 4430155 [No Abstract] [Full Text] [Related]
2. Detection of inborn errors of metabolism. III. Defects in urea cycle metabolism. Hill HZ; Goodman SI Clin Genet; 1974; 6(2):79-81. PubMed ID: 4430156 [No Abstract] [Full Text] [Related]
3. Methylmalonyl coenzyme A racemase defect: another cause of methylmalonic aciduria. Kang ES; Snodgrass PJ; Gerald PS Pediatr Res; 1972 Dec; 6(12):875-9. PubMed ID: 4643536 [No Abstract] [Full Text] [Related]
11. Methylmalonic aciduria: metabolic block localization and vitamin B 12 dependency. Rosenberg LE; Lilljeqvist A; Hsia YE Science; 1968 Nov; 162(3855):805-7. PubMed ID: 5686220 [TBL] [Abstract][Full Text] [Related]
12. Genetic defects of cobalamin metabolism. Rennert OM Ann Clin Lab Sci; 1980; 10(4):356-60. PubMed ID: 7447389 [TBL] [Abstract][Full Text] [Related]
13. Inherited defects of B12 metabolism. Mahoney MJ; Rosenberg LE Am J Med; 1970 May; 48(5):584-93. PubMed ID: 4912932 [No Abstract] [Full Text] [Related]
14. Vitamin B12-dependent methylmalonicaciduria: amino acid toxicity, long chain ketonuria, and protective effect of vitamin B12. Hsia YE; Lilljeqvist AC; Rosenberg LE Pediatrics; 1970 Oct; 46(4):497-507. PubMed ID: 5503685 [No Abstract] [Full Text] [Related]
15. Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells. Willard HF; Ambani LM; Hart AC; Mahoney MJ; Rosenberg LE Hum Genet; 1976 Dec; 34(3):277-83. PubMed ID: 1002151 [TBL] [Abstract][Full Text] [Related]
16. Studies on cultured fibroblasts from patients with defects of biotin-dependent carboxylation. Bartlett K; Ng H; Dale G; Green A; Leonard JV J Inherit Metab Dis; 1981; 4(4):183-9. PubMed ID: 6118468 [No Abstract] [Full Text] [Related]
17. Methylmalonic and propionic acidemias: lipid profiles of normal and affected human skin fibroblasts incubated with [1-14C]propionate. Giudici TA; Chen RG; Oizumi J; Shaw KN; Ng WG; Donnell GN Biochem Med Metab Biol; 1986 Jun; 35(3):384-98. PubMed ID: 2872907 [TBL] [Abstract][Full Text] [Related]
18. Beta-ketothiolase deficiency as a cause of the "ketotic hyperglycinemia syndrome". Hillman RE; Keating JP Pediatrics; 1974 Feb; 53(2):221-5. PubMed ID: 4812006 [No Abstract] [Full Text] [Related]
19. Evaluation of biotin responsiveness in cultured fibroblasts from patients with propionic acidemia: absence of response by structurally altered carboxylases. Wolf B Biochem Genet; 1979 Aug; 17(7-8):709-13. PubMed ID: 540014 [TBL] [Abstract][Full Text] [Related]
20. Metabolic cooperation among cell lines from patients with inborn errors of vitamin B12 metabolism: differential response of cblC and cblD. Byck S; Rosenblatt DS Clin Invest Med; 1991 Apr; 14(2):153-9. PubMed ID: 1676355 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]