BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 5686220)

  • 1. Methylmalonic aciduria: metabolic block localization and vitamin B 12 dependency.
    Rosenberg LE; Lilljeqvist A; Hsia YE
    Science; 1968 Nov; 162(3855):805-7. PubMed ID: 5686220
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Methylmalonyl coenzyme A racemase defect: another cause of methylmalonic aciduria.
    Kang ES; Snodgrass PJ; Gerald PS
    Pediatr Res; 1972 Dec; 6(12):875-9. PubMed ID: 4643536
    [No Abstract]   [Full Text] [Related]  

  • 3. Vitamin B12 dependent methylmalonicaciduria: defective B12 metabolism in cultured fibroblasts.
    Rosenberg LE; Lilljeqvist AC; Hsia YE; Rosenbloom FM
    Biochem Biophys Res Commun; 1969 Nov; 37(4):607-14. PubMed ID: 5353892
    [No Abstract]   [Full Text] [Related]  

  • 4. In vitro "responsive" methylmalonic acidemia: a new variant.
    Kaye CI; Morrow G; Nadler HL
    J Pediatr; 1974 Jul; 85(1):55-9. PubMed ID: 4852378
    [No Abstract]   [Full Text] [Related]  

  • 5. Defective propionate carboxylation in ketotic hyperglycinaemia.
    Hsia YE; Scully KJ; Rosenberg LE
    Lancet; 1969 Apr; 1(7598):757-8. PubMed ID: 4180220
    [No Abstract]   [Full Text] [Related]  

  • 6. A derangement in B12 metabolism associated with homocystinemia, cystathioninemia, hypomethioninemia and methylmalonic aciduria.
    Levy HL; Mudd SH; Schulman JD; Dreyfus PM; Abeles RH
    Am J Med; 1970 Mar; 48(3):390-7. PubMed ID: 5435651
    [No Abstract]   [Full Text] [Related]  

  • 7. Methylmalonic aciduria without vitamin B12 deficiency in an adult sibship.
    Giorgio AJ; Trowbridge M; Boone AW; Patten RS
    N Engl J Med; 1976 Aug; 295(6):310-3. PubMed ID: 6909
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 3-hydroxypropionate: significance of -oxidation of propionate in patients with propionic acidemia and methylmalonic acidemia.
    Ando T; Rasmussen K; Nyhan WL; Hull D
    Proc Natl Acad Sci U S A; 1972 Oct; 69(10):2807-11. PubMed ID: 4507604
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Methylmalonic aciduria. An inborn error leading to metabolic acidosis, long-chain ketonuria and intermittent hyperglycinemia.
    Rosenberg LE; Lilljeqvist AC; Hsia YE
    N Engl J Med; 1968 Jun; 278(24):1319-22. PubMed ID: 5648598
    [No Abstract]   [Full Text] [Related]  

  • 10. Methylmalonic acid.
    Barness LA
    Pediatrics; 1973 Jun; 51(6):1012-5. PubMed ID: 4710435
    [No Abstract]   [Full Text] [Related]  

  • 11. [Methylmalonic aciduria. Classification, diagnosis and therapy (author's transl)].
    Leupold D
    Klin Wochenschr; 1977 Jan; 55(2):57-63. PubMed ID: 319293
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Congenital methylmalonic acidemia: enzymatic evidence for two forms of the disease.
    Morrow G; Barness LA; Cardinale GJ; Abeles RH; Flaks JG
    Proc Natl Acad Sci U S A; 1969 May; 63(1):191-7. PubMed ID: 5257962
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Vitamin-B12-dependent methylmalonic acidemia in twins].
    Karsten J; Hansen HG; Heuer R; Wulff UC; Kneer J
    Monatsschr Kinderheilkd; 1983 May; 131(5):289-92. PubMed ID: 6877249
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Effect of vitamin B 12 deprivation on CoA intermediates related to propionate metabolism.
    Nutr Rev; 1975 Mar; 33(3):85-7. PubMed ID: 235750
    [No Abstract]   [Full Text] [Related]  

  • 16. Congenital methylmalonic acidemia: a variant of the B12 'non-responsive' form with evidence for reduced affinity of methylmalonyl-CoA mutase for its B12-coenzyme.
    Baumgartner ER; Bachmann C; Wick H
    Enzyme; 1976; 21(6):553-67. PubMed ID: 12939
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Deranged B 12 metabolism: studies of fibroblasts grown in tissue culture.
    Mudd SH; Uhlendorf BW; Hinds KR
    Biochem Med; 1970 Nov; 4(3):215-39. PubMed ID: 5524065
    [No Abstract]   [Full Text] [Related]  

  • 18. Hereditary transcobalamin II deficiency: the role of transcobalamin II in vitamin B 12 -mediated reactions.
    Scott CR; Hakami N; Teng CC; Sagerson RN
    J Pediatr; 1972 Dec; 81(6):1106-11. PubMed ID: 4643028
    [No Abstract]   [Full Text] [Related]  

  • 19. Homocystinuria with methylmalonic aciduria: two cases in a sibship.
    Goodman SI; Moe PG; Hammond KB; Mudd SH; Uhlendorf BW
    Biochem Med; 1970 Dec; 4(5):500-15. PubMed ID: 5524089
    [No Abstract]   [Full Text] [Related]  

  • 20. Studies on cultured fibroblasts in a case of methylmalonic aciduria.
    Davidson JS; Lloyd A; Christianson A; Harley EH; Berger GM
    S Afr Med J; 1984 Feb; 65(7):257-60. PubMed ID: 6141644
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.