BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

469 related articles for article (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; 310(11):686-90. PubMed ID: 6700644
    [TBL] [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; 74(6):2149-56. PubMed ID: 6511919
    [TBL] [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; 78(1):51-4. PubMed ID: 3725502
    [TBL] [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; 26(2):377-83. PubMed ID: 3812589
    [TBL] [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; 69(4):1128-33. PubMed ID: 3828532
    [TBL] [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; 17(2):94-9. PubMed ID: 2873525
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    [TBL] [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; 81(6):1690-4. PubMed ID: 3384945
    [TBL] [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; 20(6):731-41. PubMed ID: 9427140
    [TBL] [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; 34(3):427-34. PubMed ID: 2688421
    [TBL] [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; 14(2):153-9. PubMed ID: 1676355
    [TBL] [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; 34(5):483-96. PubMed ID: 43301
    [TBL] [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; 71(4):384-90. PubMed ID: 9286442
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lessons in biology from patients with inborn errors of vitamin B12 metabolism.
    Watkins D; Rosenblatt DS
    Biochimie; 2013 May; 95(5):1019-22. PubMed ID: 23402785
    [TBL] [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; 157C(1):33-44. PubMed ID: 21312325
    [TBL] [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; 3(4):329-44. PubMed ID: 8775094
    [TBL] [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; 59(4):832-7. PubMed ID: 7037072
    [TBL] [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; 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; 119():355-376. PubMed ID: 35337626
    [TBL] [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; 151(11):818-20. PubMed ID: 1468456
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.