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24. Occurrences of methylmalonic aciduria and Hartnup disorder in the same family. Shih VE; Coulombe JT; Wadman SK; Duran M; Waelkens JJ Clin Genet; 1984 Sep; 26(3):216-20. PubMed ID: 6478642 [TBL] [Abstract][Full Text] [Related]
25. Heart failure in a patient with methylmalonic acidemia. Azar MR; Shakiba M; Tafreshi RI; Rashed MS Mol Genet Metab; 2007; 92(1-2):188. PubMed ID: 17591451 [No Abstract] [Full Text] [Related]
26. Creatine metabolism in combined methylmalonic aciduria and homocystinuria. Bodamer OA; Sahoo T; Beaudet AL; O'Brien WE; Bottiglieri T; Stöckler-Ipsiroglu S; Wagner C; Scaglia F Ann Neurol; 2005 Apr; 57(4):557-60. PubMed ID: 15786446 [TBL] [Abstract][Full Text] [Related]
27. Methylmalonic acidemia, cobalamin C type, presenting with cutaneous manifestations. Howard R; Frieden IJ; Crawford D; McCalmont T; Levy ML; Rosenblatt DS; Sweetman L; Goodman SI; Ohnstad C; Hart K; Berrios M; Packman S Arch Dermatol; 1997 Dec; 133(12):1563-6. PubMed ID: 9420542 [TBL] [Abstract][Full Text] [Related]
28. Erythroblastopenia associated with methylmalonic aciduria. Case report and in vitro studies. Corazza F; Blum D; Clercx A; Mardens Y; Fondu P Biol Neonate; 1996; 70(5):304-10. PubMed ID: 8955917 [TBL] [Abstract][Full Text] [Related]
31. Genetic and biochemical approach to early prenatal diagnosis in a family with mut methylmalonic aciduria. Cavicchi C; Donati MA; Funghini S; la Marca G; Malvagia S; Ciani F; Poggi GM; Pasquini E; Zammarchi E; Morrone A Clin Genet; 2006 Jan; 69(1):72-6. PubMed ID: 16451139 [TBL] [Abstract][Full Text] [Related]
32. Continuous hemodiafiltration in the treatment of hyperammonemia due to methylmalonic acidemia. Chen CY; Tsai TC; Lee WJ; Chen HC Ren Fail; 2007; 29(6):751-4. PubMed ID: 17763173 [TBL] [Abstract][Full Text] [Related]
33. Mild form of methylmalonic aciduria misdiagnosed as propionic acidaemia during a ketotic crisis. de Almeida IT; Duran M; Silva MF; Portela R; Cabral A; Tasso T; Eusébio F; Silveira C J Inherit Metab Dis; 1991; 14(2):259-62. PubMed ID: 1886409 [No Abstract] [Full Text] [Related]
34. [Neonatal onset methylmalonic aciduria and homocystinuria:Biochemical and clinical improvement with betaine therapy]. Urbón Artero A; Aldana Gómez J; Reig Del Moral C; Nieto Conde C; Merinero Cortés B An Esp Pediatr; 2002 Apr; 56(4):337-41. PubMed ID: 11927078 [TBL] [Abstract][Full Text] [Related]
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38. [Vitamin B 12 responsive methylmalenic aciduria. Apropos of a new case]. Sann L; Divry P; Rolland MO; Bourgeois J; Bethenod M Pediatrie; 1980; 35(3):205-12. PubMed ID: 7393687 [No Abstract] [Full Text] [Related]
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40. A homozygous nonsense mutation in the methylmalonyl-CoA epimerase gene (MCEE) results in mild methylmalonic aciduria. Bikker H; Bakker HD; Abeling NG; Poll-The BT; Kleijer WJ; Rosenblatt DS; Waterham HR; Wanders RJ; Duran M Hum Mutat; 2006 Jul; 27(7):640-3. PubMed ID: 16752391 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]