These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

89 related articles for article (PubMed ID: 7421860)

  • 1. [Convulsions in an infant with biotin-dependent 3-methylcrotonylglycinuria].
    Lehnert W; Niederhoff H; Saule H
    Monatsschr Kinderheilkd (1902); 1980 May; 128(5):380-1. PubMed ID: 7421860
    [No Abstract]   [Full Text] [Related]  

  • 2. Child with a defect in leucine metabolism associated with beta-hydroxyisovaleric aciduria and beta-methylcrotonylglycinuria.
    Gompertz D; Bartlett K; Blair D; Stern CM
    Arch Dis Child; 1973 Dec; 48(12):975-7. PubMed ID: 4765660
    [No Abstract]   [Full Text] [Related]  

  • 3. A case of biotin-responsive 3-methylcrotonylglycin- and 3-hydroxyisovaleric aciduria.
    Lehnert W; Niederhoff H; Junker A; Saule H; Frasch W
    Eur J Pediatr; 1979 Oct; 132(2):107-14. PubMed ID: 499258
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Biotin-responsive beta-methylcrotonylglycinuria.
    Gompertz D; Draffan GH; Watts JL; Hull D
    Lancet; 1971 Jul; 2(7714):22-4. PubMed ID: 4103667
    [No Abstract]   [Full Text] [Related]  

  • 5. Inherited disorders of 3-methylcrotonyl CoA carboxylation.
    Leonard JV; Seakins JW; Bartlett K; Hyde J; Wilson J; Clayton B
    Arch Dis Child; 1981 Jan; 56(1):53-9. PubMed ID: 7469453
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Leucine-sensitive hypoglycaemia and its treatment with diazoxide (author's transl)].
    Reich H; Schünke W
    Monatsschr Kinderheilkd (1902); 1976 Sep; 129(9):673-6. PubMed ID: 979990
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Evidence for the enzymic defect in beta-methylcrotonylglycinuria.
    Gompertz D; Goodey PA; Bartlett K
    FEBS Lett; 1973 May; 32(1):13-4. PubMed ID: 4715674
    [No Abstract]   [Full Text] [Related]  

  • 8. Use of cofactors in inborn errors of amino acid metabolism.
    Rosenberg LE
    Curr Concepts Nutr; 1979; 8():55-64. PubMed ID: 160862
    [No Abstract]   [Full Text] [Related]  

  • 9. [Association of leucinosis and fibroelastosis. Findings on a clinical case].
    Feldioreanu T; Ciofu C; Ciofu E; Eşanu M
    Pediatria (Bucur); 1973; 22(5):461-8. PubMed ID: 4275222
    [No Abstract]   [Full Text] [Related]  

  • 10. [Inborn errors of amino acid metabolism and convulsions].
    Endo F
    Ryoikibetsu Shokogun Shirizu; 2002; (37 Pt 6):157-61. PubMed ID: 12483852
    [No Abstract]   [Full Text] [Related]  

  • 11. The neonatal form of biotin-responsive multiple carboxylase deficiency.
    Packman S; Sweetman L; Baker H; Wall S
    J Pediatr; 1981 Sep; 99(3):418-20. PubMed ID: 7264798
    [No Abstract]   [Full Text] [Related]  

  • 12. Biotin-responsive multiple carboxylase deficiency of infantile onset.
    Packman S; Sweetman L; Yoshino M; Baker H; Cowan M
    J Pediatr; 1981 Sep; 99(3):421-3. PubMed ID: 7264799
    [No Abstract]   [Full Text] [Related]  

  • 13. Beta-methylcrotonyl-CoA carboxylase deficiency: a new metabolic error in leucine degradation.
    Stokke O; Eldjarn L; Jellum E; Pande H; Waaler PE
    Pediatrics; 1972 May; 49(5):726-35. PubMed ID: 5035417
    [No Abstract]   [Full Text] [Related]  

  • 14. Propionyl-CoA carboxylase deficiency in a patient with biotin-responsive 3-methylcrotonylglycinuria.
    Sweetman L; Bates SP; Hull D; Nyhan WL
    Pediatr Res; 1977 Nov; 11(11):1144-7. PubMed ID: 917614
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Inborn errors of amino acid metabolism treatable with B group vitamins: synoptic aspects].
    Cardi E
    Acta Vitaminol Enzymol; 1980; 2(3-4):124-9. PubMed ID: 7246391
    [No Abstract]   [Full Text] [Related]  

  • 16. Organic aciduria. Treatable cause of floppy infant syndrome.
    Keeton BR
    Arch Dis Child; 1976 Aug; 51(8):636-8. PubMed ID: 962376
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Secondary cystathioninuria.
    von Studnitz W
    Acta Paediatr Scand; 1969 Mar; 58(2):173-7. PubMed ID: 5385504
    [No Abstract]   [Full Text] [Related]  

  • 18. [Strychnine in non-ketotic hyperglycinemia].
    Arenz B; Rister M; Sanchez A
    Monatsschr Kinderheilkd; 1982 Aug; 130(8):621-3. PubMed ID: 7133018
    [No Abstract]   [Full Text] [Related]  

  • 19. [Inborn disorders of amino acid metabolism as etiologic factors in progressive encephalopathy in the early neonatal period].
    Branković D; Karović D; Jovanović R; Sindić V; Erac O; Ganović R; Tomović S
    Jugosl Ginekol Perinatol; 1989; 29(1-2):33-6. PubMed ID: 2739435
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Isovaleric acidemia combined with hypertrophic pylorstenosis (author's transl)].
    Lehnert W; Schenck W; Niederhoff H
    Klin Padiatr; 1979 Sep; 191(5):477-82. PubMed ID: 574579
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.