BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

212 related articles for article (PubMed ID: 5503685)

  • 1. Vitamin B12-dependent methylmalonicaciduria: amino acid toxicity, long chain ketonuria, and protective effect of vitamin B12.
    Hsia YE; Lilljeqvist AC; Rosenberg LE
    Pediatrics; 1970 Oct; 46(4):497-507. PubMed ID: 5503685
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. American Academy of Pediatrics. Committee on Nutrition: special diets for infants with inborn errors of amino acid metabolism.
    Pediatrics; 1976 May; 57(5):783-92. PubMed ID: 940719
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Vitamin B12 dependency and cobalt-dependent metabolism.
    Scriver CR
    Pediatrics; 1970 Oct; 46(4):493-6. PubMed ID: 5503684
    [No Abstract]   [Full Text] [Related]  

  • 6. Methylmalonic acid excretion in methylmalonic acidemia.
    Kelly S; Cowger M
    N Y State J Med; 1980 Feb; 80(2):240-3. PubMed ID: 6929423
    [No Abstract]   [Full Text] [Related]  

  • 7. Beta-ketothiolase deficiency as a cause of the "ketotic hyperglycinemia syndrome".
    Hillman RE; Keating JP
    Pediatrics; 1974 Feb; 53(2):221-5. PubMed ID: 4812006
    [No Abstract]   [Full Text] [Related]  

  • 8. Response to dietary therapy in B 12 unresponsive methylmalonic acidemia.
    Nyhan WL; Fawcett N; Ando T; Rennert OM; Julius RL
    Pediatrics; 1973 Mar; 51(3):539-48. PubMed ID: 4707869
    [No Abstract]   [Full Text] [Related]  

  • 9. [Dietetics in hereditary enzyme deficiencies].
    Royer P
    Sem Hop; 1970 Feb; 46(10):653-9. PubMed ID: 4314674
    [No Abstract]   [Full Text] [Related]  

  • 10. Propionicacidemia (ketotic hyperglycinemia): dietary treatment resulting in normal growth and development.
    Brandt IK; Hsia YE; Clement DH; Provence SA
    Pediatrics; 1974 Mar; 53(3):391-5. PubMed ID: 4815259
    [No Abstract]   [Full Text] [Related]  

  • 11. Inborn errors of organic acid metabolism.
    Gompertz D
    Clin Endocrinol Metab; 1974 Mar; 3(1):107-30. PubMed ID: 4609643
    [No Abstract]   [Full Text] [Related]  

  • 12. [Value of peritoneal dialysis in the emergency treatment of metabolic diseases of constitutional origin revealed in the neonatal period].
    Saudubray JM; Fournet JP; Cloup M
    Ann Med Interne (Paris); 1971 Dec; 122(12):1279-83. PubMed ID: 5151629
    [No Abstract]   [Full Text] [Related]  

  • 13. [13C]Valine metabolism in methylmalonicacidemia using nuclear magnetic resonance: propinonate as an obligate intermediate.
    Tanaka K; Armitage IM; Ramsdell HS; Hsia YE; Lipsky SR; Rosenberg LE
    Proc Natl Acad Sci U S A; 1975 Sep; 72(9):3692-6. PubMed ID: 1059159
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Effects of protein or amino acid deprivation on the tissue distribution of vitamin B12.
    Aschkenasy A
    Isr J Med Sci; 1965 Jul; 1(4):709-11. PubMed ID: 5856102
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Studies in a patient with methylmalonic acidemia.
    Morrow G; Barness LA
    J Pediatr; 1969 May; 74(5):691-8. PubMed ID: 5778825
    [No Abstract]   [Full Text] [Related]  

  • 18. [Prognosis of congenital methylmalonic aciduria. Correlations between tolerance to proteins, response to vitamin B12 and enzymatic defect (author's transl)].
    Saudubray JM; Charpentier C; Coude FX; Ogier H; Pham Dinh D; Bartlett K; Gompertz D
    Arch Fr Pediatr; 1980; 37 Suppl 2():IX-XIV. PubMed ID: 6108749
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hyperglycinemia with ketosis due to a defect in isoleucine metabolism: a preliminary report.
    Keating JP; Feigin RD; Tenenbaum SM; Hillman RE
    Pediatrics; 1972 Dec; 50(6):890-5. PubMed ID: 4636454
    [No Abstract]   [Full Text] [Related]  

  • 20. Clinical consequences of disorders in the intermediate metabolism of branched chain amino acids (valine, leucine and isoleucine).
    Mogoş T; Cheţa CP; Mincu IT
    Rom J Intern Med; 1994; 32(1):57-61. PubMed ID: 8081313
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.