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Journal Abstract Search

452 related items for PubMed ID: 6511919

  • 21. Methionine auxotrophy in inborn errors of cobalamin metabolism.
    Garovic-Kocic V, Rosenblatt DS.
    Clin Invest Med; 1992 Aug; 15(4):395-400. PubMed ID: 1516297
    [Abstract] [Full Text] [Related]

  • 22. Cobalamins in fibroblasts cultured from normal control subjects and patients with methylmalonic aciduria.
    Linnell JC, Matthews DM, Mudd SH, Uhlendorf BW, Wise IJ.
    Pediatr Res; 1976 Mar; 10(3):179-83. PubMed ID: 2896
    [Abstract] [Full Text] [Related]

  • 23. Folate-responsive homocystinuria and megaloblastic anaemia in a female patient with functional methionine synthase deficiency (cblE disease).
    Fowler B, Schutgens RB, Rosenblatt DS, Smit GP, Lindemans J.
    J Inherit Metab Dis; 1997 Nov; 20(6):731-41. PubMed ID: 9427140
    [Abstract] [Full Text] [Related]

  • 24. Inherited defects of cobalamin metabolism.
    Watkins D, Rosenblatt DS.
    Vitam Horm; 2022 Nov; 119():355-376. PubMed ID: 35337626
    [Abstract] [Full Text] [Related]

  • 25. Preoperative methionine loading enhances restoration of the cobalamin-dependent enzyme methionine synthase after nitrous oxide anesthesia.
    Christensen B, Guttormsen AB, Schneede J, Riedel B, Refsum H, Svardal A, Ueland PM.
    Anesthesiology; 1994 May; 80(5):1046-56. PubMed ID: 8017644
    [Abstract] [Full Text] [Related]

  • 26. Nitrous oxide has multiple deleterious effects on cobalamin metabolism and causes decreases in activities of both mammalian cobalamin-dependent enzymes in rats.
    Kondo H, Osborne ML, Kolhouse JF, Binder MJ, Podell ER, Utley CS, Abrams RS, Allen RH.
    J Clin Invest; 1981 May; 67(5):1270-83. PubMed ID: 6112240
    [Abstract] [Full Text] [Related]

  • 27. 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 May; 34(5):465-82. PubMed ID: 528229
    [Abstract] [Full Text] [Related]

  • 28. The cblD defect causes either isolated or combined deficiency of methylcobalamin and adenosylcobalamin synthesis.
    Suormala T, Baumgartner MR, Coelho D, Zavadakova P, Kozich V, Koch HG, Berghaüser M, Wraith JE, Burlina A, Sewell A, Herwig J, Fowler B.
    J Biol Chem; 2004 Oct 08; 279(41):42742-9. PubMed ID: 15292234
    [Abstract] [Full Text] [Related]

  • 29. [A rare inborn error of intracellular processing of cobalamine presenting with microcephalus and megaloblastic anemia: a report of 3 children].
    Müller P, Horneff G, Hennermann JB.
    Klin Padiatr; 2007 Oct 08; 219(6):361-7. PubMed ID: 18050048
    [Abstract] [Full Text] [Related]

  • 30. Megaloblastic anaemia and disorders affecting utilisation of vitamin B12 and folate in childhood.
    Cooper BA.
    Clin Haematol; 1976 Oct 08; 5(3):631-59. PubMed ID: 788982
    [No Abstract] [Full Text] [Related]

  • 31. Clinical and molecular heterogeneity in patients with the cblD inborn error of cobalamin metabolism.
    Miousse IR, Watkins D, Coelho D, Rupar T, Crombez EA, Vilain E, Bernstein JA, Cowan T, Lee-Messer C, Enns GM, Fowler B, Rosenblatt DS.
    J Pediatr; 2009 Apr 08; 154(4):551-6. PubMed ID: 19058814
    [Abstract] [Full Text] [Related]

  • 32. Mitochondrial vitamin B12-binding proteins in patients with inborn errors of cobalamin metabolism.
    Moras E, Hosack A, Watkins D, Rosenblatt DS.
    Mol Genet Metab; 2007 Feb 08; 90(2):140-7. PubMed ID: 17011224
    [Abstract] [Full Text] [Related]

  • 33. 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 08; 57(4):557-60. PubMed ID: 15786446
    [Abstract] [Full Text] [Related]

  • 34. Transcobalamin II deficiency presenting with methylmalonic aciduria and homocystinuria and abnormal absorption of cobalamin.
    Barshop BA, Wolff J, Nyhan WL, Yu A, Prodanos C, Jones G, Sweetman L, Leslie J, Holm J, Green R.
    Am J Med Genet; 1990 Feb 08; 35(2):222-8. PubMed ID: 2309761
    [Abstract] [Full Text] [Related]

  • 35. Gene identification for the cblD defect of vitamin B12 metabolism.
    Coelho D, Suormala T, Stucki M, Lerner-Ellis JP, Rosenblatt DS, Newbold RF, Baumgartner MR, Fowler B.
    N Engl J Med; 2008 Apr 03; 358(14):1454-64. PubMed ID: 18385497
    [Abstract] [Full Text] [Related]

  • 36. The effects of nitrous oxide on cobalamins, folates, and on related events.
    Chanarin I.
    Crit Rev Toxicol; 1982 Sep 03; 10(3):179-213. PubMed ID: 6127188
    [Abstract] [Full Text] [Related]

  • 37. Changes in cobalamin metabolism are associated with the altered methionine auxotrophy of highly growth autonomous human melanoma cells.
    Liteplo RG, Hipwell SE, Rosenblatt DS, Sillaots S, Lue-Shing H.
    J Cell Physiol; 1991 Nov 03; 149(2):332-8. PubMed ID: 1748723
    [Abstract] [Full Text] [Related]

  • 38. Lessons in biology from patients with inborn errors of vitamin B12 metabolism.
    Watkins D, Rosenblatt DS.
    Biochimie; 2013 May 03; 95(5):1019-22. PubMed ID: 23402785
    [Abstract] [Full Text] [Related]

  • 39. Identification and perturbation of mutant human fibroblasts based on measurements of methylmalonic acid and total homocysteine in the culture media.
    Kolhouse JF, Stabler SP, Allen RH.
    Arch Biochem Biophys; 1993 Jun 03; 303(2):355-60. PubMed ID: 8099783
    [Abstract] [Full Text] [Related]

  • 40. Structure of Human B12 Trafficking Protein CblD Reveals Molecular Mimicry and Identifies a New Subfamily of Nitro-FMN Reductases.
    Yamada K, Gherasim C, Banerjee R, Koutmos M.
    J Biol Chem; 2015 Dec 04; 290(49):29155-66. PubMed ID: 26364851
    [Abstract] [Full Text] [Related]

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