BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 4812006)

  • 1. 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]  

  • 2. A defect in l-isoleucine metabolism associated with alpha-methyl-beta-hydroxybutyric and alpha-methylacetoacetic aciduria: quantitative in vivo and in vitro studies.
    Gompertz D; Saudubray JM; Charpentier C; Bartlett K; Goodey PA; Draffan GH
    Clin Chim Acta; 1974 Dec; 57(3):269-81. PubMed ID: 4434646
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. A block in glycine cleavage reaction as a common mechanism in ketotic and nonketotic hyperglycinemia.
    Tada K
    Pediatr Res; 1974 Jul; 8(7):721-3. PubMed ID: 4837569
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. The identification of (E)-2-methylglutaconic acid, a new isoleucine metabolite, in the urine of patients with beta-ketothiolase deficiency, propionic acidaemia and methylmalonic acidaemia.
    Duran M; Bruinvis L; Ketting D; Kamerling JP; Wadman SK; Schutgens RB
    Biomed Mass Spectrom; 1982 Jan; 9(1):1-5. PubMed ID: 7059658
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Acute neonatal nonketotic hyperglycinemia: normal propionate and methylmalonate metabolism.
    Baumgartner ER; Bachmann C; Brechbühler T; Wick H
    Pediatr Res; 1975 Jul; 9(7):559-64. PubMed ID: 240144
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An inherited disorder of isoleucine catabolism causing accumulation of alpha-methylacetoacetate and alpha-methyl-beta -hydroxybutyrate, and intermittent metabolic acidosis.
    Daum RS; Scriver CR; Mamer OA; Delvin E; Lamm P; Goldman H
    Pediatr Res; 1973 Mar; 7(3):149-60. PubMed ID: 4690360
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Propionic acidemia in patients with ketotic hyperglycinemia.
    Ando T; Rasmussen K; Nyhan WL; Donnell GN; Barnes ND
    J Pediatr; 1971 May; 78(5):827-32. PubMed ID: 5581587
    [No Abstract]   [Full Text] [Related]  

  • 12. The oxidation of glycine and propionic acid in propionic acidemia with ketotic hyperglycinemia.
    Ando T; Nyhan WL; Connor JD; Rasmussen K; Donnell G; Barnes N; Cottom D; Hull D
    Pediatr Res; 1972 Jun; 6(6):576-83. PubMed ID: 5046977
    [No Abstract]   [Full Text] [Related]  

  • 13. Normal propionate metabolism in "non-ketotic hyperglycinemia".
    Baumgartner ER; Wick H
    N Engl J Med; 1972 Apr; 286(14):784-5. PubMed ID: 5025792
    [No Abstract]   [Full Text] [Related]  

  • 14. Inhibition of glycine oxidation in cultured fibroblasts by isoleucine.
    Hillman RE; Sowers LH; Cohen JL
    Pediatr Res; 1973 Dec; 7(12):945-7. PubMed ID: 4753048
    [No Abstract]   [Full Text] [Related]  

  • 15. [Propionic acidemia. New concept of hyperglycinemia with ketosis].
    Guibaud P
    Pediatrie; 1972 Mar; 27(2):217-20. PubMed ID: 4557792
    [No Abstract]   [Full Text] [Related]  

  • 16. Non-ketotic hyperglycinemia in two sibs with mild psycho-neurological symptoms.
    Holmgren G; son Blomquist HK
    Neuropadiatrie; 1977 Feb; 8(1):67-72. PubMed ID: 576734
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Acetoacetyl CoA thiolase deficiency presenting as ketotic hypoglycemia.
    Leonard JV; Middleton B; Seakins JW
    Pediatr Res; 1987 Feb; 21(2):211-3. PubMed ID: 2881245
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Beta-ketothiolase deficiency brought with lethargy: case report.
    Arica V; Arica SG; Dag H; Onur H; Obut O; Gülbayzar S
    Hum Exp Toxicol; 2011 Oct; 30(10):1724-7. PubMed ID: 21247997
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Beta-ketothiolase deficiency: a case of ketoacidosis with hyperglycinemia].
    Elleau C; Parrot-Roulaud F; Perel Y; Divry P; Rolland MO; Zabot MT; Middleton R; Guillard JM
    Pediatrie; 1992; 47(3):185-9. PubMed ID: 1319041
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 2-Ethylhydracrylic acid: a newly described urinary organic acid.
    Mamer OA; Tjoa SS
    Clin Chim Acta; 1974 Sep; 55(2):199-204. PubMed ID: 4458986
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.