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42. Antibiotic therapy for improvement of metabolic control in methylmalonic aciduria. Koletzko B; Bachmann C; Wendel U J Pediatr; 1990 Jul; 117(1 Pt 1):99-101. PubMed ID: 2370620 [No Abstract] [Full Text] [Related]
43. [Outcomes of patients with combined methylmalonic acidemia and homocystinuria after treatment]. Huang Z; Han LS; Ye J; Qiu WJ; Zhang HW; Gao XL; Wang Y; Ji WJ; Li XY; Gu XF Zhonghua Er Ke Za Zhi; 2013 Mar; 51(3):194-8. PubMed ID: 23751581 [TBL] [Abstract][Full Text] [Related]
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45. [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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49. Modulation of B12 dosage and response in fetal treatment of methylmalonic aciduria (MMA): titration of treatment dose to serum and urine MMA. Evans MI; Duquette DA; Rinaldo P; Bawle E; Rosenblatt DS; Whitty J; Quintero RA; Johnson MP Fetal Diagn Ther; 1997; 12(1):21-3. PubMed ID: 9101216 [TBL] [Abstract][Full Text] [Related]
50. Homozygous nonsense mutation in the MCEE gene and siRNA suppression of methylmalonyl-CoA epimerase expression: a novel cause of mild methylmalonic aciduria. Dobson CM; Gradinger A; Longo N; Wu X; Leclerc D; Lerner-Ellis J; Lemieux M; Belair C; Watkins D; Rosenblatt DS; Gravel RA Mol Genet Metab; 2006 Aug; 88(4):327-33. PubMed ID: 16697227 [TBL] [Abstract][Full Text] [Related]
51. [Methylmalonic aciduria. A case report]. van Dyk JC; Meiring JL; Prinsloo JG S Afr Med J; 1982 Oct; 62(19):700-2. PubMed ID: 7135128 [TBL] [Abstract][Full Text] [Related]
52. [Mutation analysis of the MMACHC gene in a pedigree with methylmalonic aciduria]. Tang H; Hao H; Tang SH; Chen X; Liu F; Cha QB; Li YQ; Li HJ; Sun L; Yu M; Xiao X; Zhou TH Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):62-5. PubMed ID: 19199254 [TBL] [Abstract][Full Text] [Related]
53. Methylmalonic aciduria due to a new defect in adenosylcobalamin accumulation by cells. Cooper BA; Rosenblatt DS; Watkins D Am J Hematol; 1990 Jun; 34(2):115-20. PubMed ID: 2339678 [TBL] [Abstract][Full Text] [Related]
54. L-Carnitine insufficiency in disorders of organic acid metabolism: response to L-carnitine by patients with methylmalonic aciduria and 3-hydroxy-3-methylglutaric aciduria. Chalmers RA; Stacey TE; Tracey BM; de Sousa C; Roe CR; Millington DS; Hoppel CL J Inherit Metab Dis; 1984; 7 Suppl 2():109-10. PubMed ID: 6207380 [No Abstract] [Full Text] [Related]
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56. Congenital defect in intracellular cobalamin metabolism resulting in homocysteinuria and methylmalonic aciduria. I. Case report and histopathology. Baumgartner ER; Wick H; Maurer R; Egli N; Steinmann B Helv Paediatr Acta; 1979; 34(5):465-82. PubMed ID: 528229 [TBL] [Abstract][Full Text] [Related]
57. Accumulation of odd-numbered long-chain fatty acids in fetuses and neonates with inherited disorders of propionate metabolism. Wendel U; Baumgartner R; van der Meer SB; Spaapen LJ Pediatr Res; 1991 Apr; 29(4 Pt 1):403-5. PubMed ID: 1852536 [TBL] [Abstract][Full Text] [Related]
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60. 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] [Previous] [Next] [New Search]