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.


PUBMED FOR HANDHELDS

Journal Abstract Search


102 related items for PubMed ID: 4734834

  • 21. Biochemical characteristics of galactokinase from adult and fetal human red cells.
    Mathai CK, Beutler E.
    Enzymologia; 1967 Oct 31; 33(3):224-30. PubMed ID: 5621948
    [No Abstract] [Full Text] [Related]

  • 22. Cataracts and galactokinase deficiency.
    Beutler E.
    N Engl J Med; 1972 Jul 27; 287(4):202-3. PubMed ID: 5033541
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. [Autoanalysis in the biochemical study of metabolic and hereditary diseases].
    Lemonnier A, Charpentier C.
    Ann Biol Clin (Paris); 1973 Jul 27; 31(6):509-24. PubMed ID: 4594986
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. [Determination of galactose-1-phosphate-uridyl-transferase activity in children with galactosemia and their relatives].
    Knapp W, Winkler G.
    Padiatr Grenzgeb; 1972 Jul 27; 11(1):35-47. PubMed ID: 5042112
    [No Abstract] [Full Text] [Related]

  • 28. Human hepatic uridine diphosphate galactose pyrophosphorylase. Its characterization and activity during development.
    Abraham HD, Howell RR.
    J Biol Chem; 1969 Feb 25; 244(4):545-50. PubMed ID: 5768855
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. Galactokinase in human red blood cells. Its dependency on galactose concentration.
    de Verdier CH.
    Scand J Clin Lab Invest Suppl; 1966 Feb 25; 18():156-7. PubMed ID: 5958515
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Hereditary orotic aciduria. I. A new case with family studies.
    Rogers LE, Warford LR, Patterson RB, Porter FS.
    Pediatrics; 1968 Sep 25; 42(3):415-22. PubMed ID: 5677482
    [No Abstract] [Full Text] [Related]

  • 33. [Determination of the galactose-1-phosphate-uridylytransferase activity in the erythocyte haemolysate of mongoloids (author's transl)].
    Nothjunge J, Most I, Hass I, Menne F.
    Z Klin Chem Klin Biochem; 1974 Feb 25; 12(2):59-61. PubMed ID: 4279511
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. [Galactokinase defect in a newborn infant].
    Linneweh F, Schaumlöffel E, Vetrella M.
    Klin Wochenschr; 1970 Jan 01; 48(1):31-3. PubMed ID: 5522111
    [No Abstract] [Full Text] [Related]

  • 36. Hyperammonemia due to a mutant enzyme of ornithine transcarbamylase.
    Matsuda I, Arashima S, Nambu H, Takekoshi Y, Anakura M.
    Pediatrics; 1971 Oct 01; 48(4):595-600. PubMed ID: 5114747
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. A fluorometric method for the assay of galactose-1-phosphate in red blood cells.
    Dahlqvist A.
    J Lab Clin Med; 1971 Dec 01; 78(6):931-8. PubMed ID: 5131857
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 6.