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16. Reliability of biochemical parameters used in prenatal diagnosis of combined methylmalonic aciduria and homocystinuria. Merinero B; Pérez-Cerdá C; Garcia MJ; Chadefaux-Vekemans B; Kamoun P; Tonetti C; Zittoun J; Jakobs C; Ugarte M Prenat Diagn; 1998 Sep; 18(9):947-52. PubMed ID: 9793978 [TBL] [Abstract][Full Text] [Related]
17. [Neonatal hemolytic-uremic syndrome, methylmalonic aciduria and homocystinuria caused by intracellular vitamin B 12 deficiency. Value of etiological diagnosis]. Chenel C; Wood C; Gourrier E; Zittoun J; Casadevall I; Ogier H Arch Fr Pediatr; 1993 Nov; 50(9):749-54. PubMed ID: 8060203 [TBL] [Abstract][Full Text] [Related]
18. Congenital methylmalonic aciduria--homocystinuria with megaloblastic anemia: observations on response to hydroxocobalamin and on the effect of homocysteine and methionine on the deoxyuridine suppression test. Carmel R; Bedros AA; Mace JW; Goodman SI Blood; 1980 Apr; 55(4):570-9. PubMed ID: 7357085 [No Abstract] [Full Text] [Related]
19. Ventricular septal defect closure in a neonate with combined methylmalonic aciduria/homocystinuria. Heinemann MK; Tomaske M; Trefz FK; Bosk A; Baden W; Ziemer G Ann Thorac Surg; 2001 Oct; 72(4):1391-2. PubMed ID: 11603477 [TBL] [Abstract][Full Text] [Related]
20. Marfanoid features in a child with combined methylmalonic aciduria and homocystinuria (CblC type). Heil SG; Hogeveen M; Kluijtmans LA; van Dijken PJ; van de Berg GB; Blom HJ; Morava E J Inherit Metab Dis; 2007 Oct; 30(5):811. PubMed ID: 17768669 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]