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5. Congenital methylmalonic acidemia: a variant of the B12 'non-responsive' form with evidence for reduced affinity of methylmalonyl-CoA mutase for its B12-coenzyme. Baumgartner ER; Bachmann C; Wick H Enzyme; 1976; 21(6):553-67. PubMed ID: 12939 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Assay of methylmalonyl CoA mutase with high-performance liquid chromatography. Kikuchi M; Hanamizu H; Narisawa K; Tada K Clin Chim Acta; 1989 Oct; 184(3):307-13. PubMed ID: 2575466 [TBL] [Abstract][Full Text] [Related]
8. Novel mutation of methylmalonyl-CoA mutase gene causing the mut0 form of methylmalonic acidemia in a Japanese girl. Oyama C; Takahashi T; Matsumori M; Shoji Y; Tajima G; Sakura N; Hasegawa Y; Yamaguchi S; Kakinuma H; Takada G Pediatr Int; 2007 Apr; 49(2):232-4. PubMed ID: 17445044 [No Abstract] [Full Text] [Related]
18. Towards metabolic sink therapy for mut methylmalonic acidaemia: retrovirus-mediated transfer of the human methylmalonyl-CoA mutase cDNA into peripheral blood progenitor cells of a child with mut methylmalonic acidaemia. Chang CC; Hsiao KJ; Chen ML; Lin CM J Inherit Metab Dis; 1999 Dec; 22(8):951-2. PubMed ID: 10604156 [No Abstract] [Full Text] [Related]
19. Methylmalonic aciduria without vitamin B12 deficiency in an adult sibship. Giorgio AJ; Trowbridge M; Boone AW; Patten RS N Engl J Med; 1976 Aug; 295(6):310-3. PubMed ID: 6909 [TBL] [Abstract][Full Text] [Related]
20. Liver transplantation is not curative for methylmalonic acidopathy caused by methylmalonyl-CoA mutase deficiency. Kaplan P; Ficicioglu C; Mazur AT; Palmieri MJ; Berry GT Mol Genet Metab; 2006 Aug; 88(4):322-6. PubMed ID: 16750411 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]