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PUBMED FOR HANDHELDS

Journal Abstract Search


162 related items for PubMed ID: 4370029

  • 1. Fructose-1,6-diphosphatase deficiency: another enzyme defect which can present itself with the clinical features of "tyrosinosis".
    Bakker HD, de Bree PK, van Sprang FJ, Wadman SK.
    Clin Chim Acta; 1974 Aug 30; 55(1):41-7. PubMed ID: 4370029
    [No Abstract] [Full Text] [Related]

  • 2. Fructosaemia-"acute-tyrosinosis".
    Lindemann R, Gjessing LR, Merton B, Halvorsen S.
    Lancet; 1969 Apr 26; 1(7600):891. PubMed ID: 4180556
    [No Abstract] [Full Text] [Related]

  • 3. Fructose I,6 diphosphatase deficiency.
    Tarlow MJ, Patrick AD, Carlton DR, Barton ME.
    Proc Nutr Soc; 1979 Dec 26; 38(3):111A. PubMed ID: 231259
    [No Abstract] [Full Text] [Related]

  • 4. Detection of fructose-1,6-diphosphatase deficiency with use of white blood cells.
    Melancon SB, Nadler HL.
    N Engl J Med; 1972 Mar 30; 286(13):731-2. PubMed ID: 4334313
    [No Abstract] [Full Text] [Related]

  • 5. Metabolic and biochemical studies in fructose 1,6-diphosphatase deficiency.
    Melancon SB, Khachadurian AK, Nadler HL, Brown BI.
    J Pediatr; 1973 Apr 30; 82(4):650-7. PubMed ID: 4349063
    [No Abstract] [Full Text] [Related]

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  • 7. Diagnosis and treatment of tyrosinosis.
    Fairney A, Francis D, Ersser RS, Seakins JW, Cottom D.
    Arch Dis Child; 1968 Oct 30; 43(231):540-7. PubMed ID: 5696464
    [No Abstract] [Full Text] [Related]

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  • 10. Abnormal tyrosine metabolism in hereditary fructose intolerance.
    Grant DB, Alexander FW, Seakins JW.
    Acta Paediatr Scand; 1970 Jul 30; 59(4):432-4. PubMed ID: 5447686
    [No Abstract] [Full Text] [Related]

  • 11. Glycerol-3-phosphate excretion in fructose-1,6-diphosphatase deficiency.
    Krywawych S, Katz G, Lawson AM, Wyatt S, Brenton DP.
    J Inherit Metab Dis; 1986 Jul 30; 9(4):388-92. PubMed ID: 3031364
    [Abstract] [Full Text] [Related]

  • 12. [Lactic acidosis, hypoglycemia and hepatomegaly due to hereditary defect in hepatic fructose-1, 6-diphosphatase].
    Saudubray JM, Dreyfus JC, Cepanec C, Le Lo'ch H, Trung PH, Mozziconacci P.
    Arch Fr Pediatr; 1973 Jul 30; 30(6):609-32. PubMed ID: 4156164
    [No Abstract] [Full Text] [Related]

  • 13. [Hypertyrosinemia with hypermethioninemia in the newborn in a case of fructose intolerance].
    Willems C, Heusden A, Renson P, Legat C, Monard Y, Stainier L.
    Helv Paediatr Acta; 1971 Oct 30; 26(4):467-81. PubMed ID: 5123311
    [No Abstract] [Full Text] [Related]

  • 14. Biochemical studies in a patient with "tyrosinosis".
    Louis WJ, Pitt DD, Davies H.
    Aust N Z J Med; 1974 Jun 30; 4(3):281-6. PubMed ID: 4531904
    [No Abstract] [Full Text] [Related]

  • 15. Infantile lactic acidosis due to hereditary fructose 1,6-diphosphatase deficiency.
    Baerlocher K, Gitzelmann R, Nüssli R, Dumermuth G.
    Helv Paediatr Acta; 1971 Dec 30; 26(5):489-506. PubMed ID: 4335192
    [No Abstract] [Full Text] [Related]

  • 16. Recovery after dietary treatment of an infant with features of tyrosinosis.
    Harries JT, Seakins JW, Ersser RS, Lloyd JK.
    Arch Dis Child; 1969 Apr 30; 44(234):258-67. PubMed ID: 5779435
    [No Abstract] [Full Text] [Related]

  • 17. Recurrent attacks of ketotic acidosis associated with fructose-1,6-diphosphatase deficiency.
    Corbeel L, Eggermont E, Eeckels R, Jaeken J, Casteels-Van Daele M, Devlieger H, Delmontte B.
    Acta Paediatr Belg; 1976 Apr 30; 29(1):29-34. PubMed ID: 189564
    [No Abstract] [Full Text] [Related]

  • 18. An exceptional case of tyrosinosis.
    Wadman SK, van Sprang FJ, Maas JW, Ketting D.
    J Ment Defic Res; 1968 Dec 30; 12(4):269-81. PubMed ID: 5729527
    [No Abstract] [Full Text] [Related]

  • 19. [Differential diagnosis between hereditary fructose intolerance and fructose-1,6-diphosphatase deficiency].
    Méndez Aparicio FM.
    Rev Clin Esp; 1968 Dec 30; 161(5-6):289-96. PubMed ID: 6270745
    [No Abstract] [Full Text] [Related]

  • 20. Detection of heterozygotes for fructose 1,6-diphosphatase deficiency by measuring fructose 1,6-diphosphatase activity in their cultured peripheral lymphocytes.
    Ito M, Kuroda Y, Kobashi H, Watanabe T, Takeda E, Toshima K, Miyao M.
    Clin Chim Acta; 1984 Aug 15; 141(1):27-32. PubMed ID: 6088124
    [Abstract] [Full Text] [Related]


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