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Journal Abstract Search

469 related items for PubMed ID: 6700644

  • 1. Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism.
    Schuh S, Rosenblatt DS, Cooper BA, Schroeder ML, Bishop AJ, Seargeant LE, Haworth JC.
    N Engl J Med; 1984 Mar 15; 310(11):686-90. PubMed ID: 6700644
    [Abstract] [Full Text] [Related]

  • 2. Altered vitamin B12 metabolism in fibroblasts from a patient with megaloblastic anemia and homocystinuria due to a new defect in methionine biosynthesis.
    Rosenblatt DS, Cooper BA, Pottier A, Lue-Shing H, Matiaszuk N, Grauer K.
    J Clin Invest; 1984 Dec 15; 74(6):2149-56. PubMed ID: 6511919
    [Abstract] [Full Text] [Related]

  • 3. New disorder of vitamin B12 metabolism (cobalamin F) presenting as methylmalonic aciduria.
    Rosenblatt DS, Laframboise R, Pichette J, Langevin P, Cooper BA, Costa T.
    Pediatrics; 1986 Jul 15; 78(1):51-4. PubMed ID: 3725502
    [Abstract] [Full Text] [Related]

  • 4. Vitamin B12 responsive homocystinuria and megaloblastic anemia: heterogeneity in methylcobalamin deficiency.
    Rosenblatt DS, Thomas IT, Watkins D, Cooper BA, Erbe RW.
    Am J Med Genet; 1987 Feb 15; 26(2):377-83. PubMed ID: 3812589
    [Abstract] [Full Text] [Related]

  • 5. Vitamin B12-responsive neonatal megaloblastic anemia and homocystinuria with associated reduced methionine synthase activity.
    Hallam LJ, Sawyer M, Clark AC, Van der Weyden MB.
    Blood; 1987 Apr 15; 69(4):1128-33. PubMed ID: 3828532
    [Abstract] [Full Text] [Related]

  • 6. A cobalamin metabolic defect with homocystinuria, methylmalonic aciduria and macrocytic anemia.
    Mamlok RJ, Isenberg JN, Rassin DK, Norcross K, Tallan HH.
    Neuropediatrics; 1986 May 15; 17(2):94-9. PubMed ID: 2873525
    [Abstract] [Full Text] [Related]

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

  • 8. Genetic heterogeneity among patients with methylcobalamin deficiency. Definition of two complementation groups, cblE and cblG.
    Watkins D, Rosenblatt DS.
    J Clin Invest; 1988 Jun 15; 81(6):1690-4. PubMed ID: 3384945
    [Abstract] [Full Text] [Related]

  • 9. 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 15; 20(6):731-41. PubMed ID: 9427140
    [Abstract] [Full Text] [Related]

  • 10. Functional methionine synthase deficiency (cblE and cblG): clinical and biochemical heterogeneity.
    Watkins D, Rosenblatt DS.
    Am J Med Genet; 1989 Nov 15; 34(3):427-34. PubMed ID: 2688421
    [Abstract] [Full Text] [Related]

  • 11. Metabolic cooperation among cell lines from patients with inborn errors of vitamin B12 metabolism: differential response of cblC and cblD.
    Byck S, Rosenblatt DS.
    Clin Invest Med; 1991 Apr 15; 14(2):153-9. PubMed ID: 1676355
    [Abstract] [Full Text] [Related]

  • 12. Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria. II. Biochemical investigations.
    Baumgartner ER, Wick H, Linnell JC, Gaull GE, Bachmann C, Steinmann B.
    Helv Paediatr Acta; 1979 Apr 15; 34(5):483-96. PubMed ID: 43301
    [Abstract] [Full Text] [Related]

  • 13. Functional methionine synthase deficiency due to cblG disorder: a report of two patients and a review.
    Harding CO, Arnold G, Barness LA, Wolff JA, Rosenblatt DS.
    Am J Med Genet; 1997 Sep 05; 71(4):384-90. PubMed ID: 9286442
    [Abstract] [Full Text] [Related]

  • 14. Lessons in biology from patients with inborn errors of vitamin B12 metabolism.
    Watkins D, Rosenblatt DS.
    Biochimie; 2013 May 05; 95(5):1019-22. PubMed ID: 23402785
    [Abstract] [Full Text] [Related]

  • 15. Inborn errors of cobalamin absorption and metabolism.
    Watkins D, Rosenblatt DS.
    Am J Med Genet C Semin Med Genet; 2011 Feb 15; 157C(1):33-44. PubMed ID: 21312325
    [Abstract] [Full Text] [Related]

  • 16. Vitamin B12 in health and disease: part I--inherited disorders of function, absorption, and transport.
    Kapadia CR.
    Gastroenterologist; 1995 Dec 15; 3(4):329-44. PubMed ID: 8775094
    [Abstract] [Full Text] [Related]

  • 17. 5-Methyltetrahydrofolate related enzymes and DNA polymerase alpha activities in bone marrow cells from patients with vitamin B12 deficient megaloblastic anemia.
    Kano Y, Sakamoto S, Hida K, Suda K, Takaku F.
    Blood; 1982 Apr 15; 59(4):832-7. PubMed ID: 7037072
    [Abstract] [Full Text] [Related]

  • 18. Cobalamin E (cblE) disease: a severe neurological disorder with megaloblastic anaemia, homocystinuria and low serum methionine.
    Steen C, Rosenblatt DS, Scheying H, Braeuer HC, Kohlschütter A.
    J Inherit Metab Dis; 1997 Sep 15; 20(5):705-6. PubMed ID: 9323567
    [No Abstract] [Full Text] [Related]

  • 19. Inherited defects of cobalamin metabolism.
    Watkins D, Rosenblatt DS.
    Vitam Horm; 2022 Sep 15; 119():355-376. PubMed ID: 35337626
    [Abstract] [Full Text] [Related]

  • 20. Biochemical diagnosis and outcome of 2 years treatment in a patient with combined methylmalonic aciduria and homocystinuria.
    Bellini C, Cerone R, Bonacci W, Caruso U, Magliano CP, Serra G, Fowler B, Romano C.
    Eur J Pediatr; 1992 Nov 15; 151(11):818-20. PubMed ID: 1468456
    [Abstract] [Full Text] [Related]

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