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3. Prenatal therapy of a patient with vitamin-B12-responsive methylmalonic acidemia. Ampola MG; Mahoney MJ; Nakamura E; Tanaka K N Engl J Med; 1975 Aug; 293(7):313-7. PubMed ID: 239344 [TBL] [Abstract][Full Text] [Related]
4. [Methylmalonic acidemia. Diagnosis and treatment in various patients]. Bakker HD; Duran M; van Gennip AH; van Sprang FJ; Wadman SK Ned Tijdschr Geneeskd; 1978 May; 122(20):707-12. PubMed ID: 26029 [No Abstract] [Full Text] [Related]
5. Methylmalonic acidaemia due to mutase apoenzyme defect: responsive to vitamin B12 in intact fibroblasts but not in vivo. Baumgartner R; Giardini O; Cantani A; Sabetta G; Castro M J Inherit Metab Dis; 1982; 5(3):137-41. PubMed ID: 6133033 [TBL] [Abstract][Full Text] [Related]
6. Recent advances in the inherited methylmalonic acidemias. Mahoney MJ; Bick D Acta Paediatr Scand; 1987 Sep; 76(5):689-96. PubMed ID: 2889315 [TBL] [Abstract][Full Text] [Related]
7. Methylmalonic/beta-hydroxy-n-valeric aciduria due to methylmalonyl-CoA mutase deficiency. Goodman SI; McCabe ER; Fennessey PV; Miles BS; Mace JW; Jellum E Clin Chim Acta; 1978 Aug; 87(3):441-9. PubMed ID: 28187 [TBL] [Abstract][Full Text] [Related]
8. [Study of a case of methylmalonic acidemia of neonatal onset. Therapeutic value of peritoneal dialysis. Discussion of vitamin B 12 sensitivity]. Saudubray JM; Boisse J; Charpentier C; Lemonnier A; Mozziconacci P Arch Fr Pediatr; 1972; 29(6):676-7. PubMed ID: 5078375 [No Abstract] [Full Text] [Related]
9. Methylmalonyl-CoA mutase activity of leukocytes in variants and heterozygotes of methylmalonic acidemia. Narisawa K; Saito T; Hisa S; Suzuki H; Hayasaka K Tohoku J Exp Med; 1977 Sep; 123(1):1-8. PubMed ID: 21471 [TBL] [Abstract][Full Text] [Related]
10. Biochemical analysis of intact fibroblasts from two cases with methylmalonic acidaemia. Kakinuma H; Ogura N; Ohtake A; Takayanagi M; Nakajima H; Kondo H; Terada H; Okuda K; Nomoto Y J Inherit Metab Dis; 1985; 8(3):151-2. PubMed ID: 2879965 [No Abstract] [Full Text] [Related]
11. Methylmalonic aciduria: a variant form of methylmalonyl coenzyme A apomutase deficiency. Wilcken B; Kilham HA; Faull K J Pediatr; 1977 Sep; 91(3):428-30. PubMed ID: 19569 [TBL] [Abstract][Full Text] [Related]
12. Methylmalonic acid excretion in methylmalonic acidemia. Kelly S; Cowger M N Y State J Med; 1980 Feb; 80(2):240-3. PubMed ID: 6929423 [No Abstract] [Full Text] [Related]
13. The natural history of the inherited methylmalonic acidemias. Matsui SM; Mahoney MJ; Rosenberg LE N Engl J Med; 1983 Apr; 308(15):857-61. PubMed ID: 6132336 [TBL] [Abstract][Full Text] [Related]
14. First trimester diagnosis of methylmalonic aciduria. Fowler B; Giles L; Sardharwalla IB; Donnai P; Clayton JK Prenat Diagn; 1988 Mar; 8(3):207-13. PubMed ID: 2897685 [TBL] [Abstract][Full Text] [Related]
15. Inborn errors of cobalamin absorption and metabolism. Watkins D; Rosenblatt DS Am J Med Genet C Semin Med Genet; 2011 Feb; 157C(1):33-44. PubMed ID: 21312325 [TBL] [Abstract][Full Text] [Related]
16. Studies of methylmalonyl-coenzyme A carbonylmutase activity in methylmalonic acidemia. II. In vitro binding kinetics with adenosylcobalamin. Morrow G; Lebowitz J Biochem Med; 1976 Jun; 15(3):241-5. PubMed ID: 11786 [No Abstract] [Full Text] [Related]