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Journal Abstract Search

209 related items for PubMed ID: 4360930

  • 1. Galactokinase deficiency in twins: clinical and biochemical studies.
    Olambiwonnu NO, McVie R, Ng WG, Frasier SD, Donnell GN.
    Pediatrics; 1974 Mar; 53(3):314-8. PubMed ID: 4360930
    [No Abstract] [Full Text] [Related]

  • 2. Some inferences from galactokinase deficiency.
    Sidbury JB.
    Pediatrics; 1974 Mar; 53(3):309-10. PubMed ID: 4360929
    [No Abstract] [Full Text] [Related]

  • 3. Galactokinase deficiency as a cause of cataracts.
    Beutler E, Matsumoto F, Kuhl W, Krill A, Levy N, Sparkes R, Degnan M.
    N Engl J Med; 1973 Jun 07; 288(23):1203-6. PubMed ID: 4700553
    [No Abstract] [Full Text] [Related]

  • 4. The lens, cataracts, and galactosemia.
    Cogan DG.
    N Engl J Med; 1973 Jun 07; 288(23):1239-40. PubMed ID: 4700558
    [No Abstract] [Full Text] [Related]

  • 5. Galactokinase deficiency: clinical and biochemical findings in a new kindred.
    Pickering WR, Howell RR.
    J Pediatr; 1972 Jul 07; 81(1):50-5. PubMed ID: 5034870
    [No Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Galactokinase-deficiency cataracts in identical twins.
    Oberman AE, Wilson WA, Frasier SD, Donnell GN, Bergren WR.
    Am J Ophthalmol; 1972 Nov 27; 74(5):887-92. PubMed ID: 4644736
    [No Abstract] [Full Text] [Related]

  • 8. [Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)].
    Brivet M, Moatti N, Lemonnier A.
    Ann Biol Clin (Paris); 1979 Nov 27; 37(5):259-70. PubMed ID: 232826
    [Abstract] [Full Text] [Related]

  • 9. Hereditary galactokinase deficiency.
    Cook JG, Don NA, Mann TP.
    Arch Dis Child; 1971 Aug 27; 46(248):465-9. PubMed ID: 5109408
    [Abstract] [Full Text] [Related]

  • 10. Cataracts, galactosuria and hypergalactosemia due to galactokinase deficiency in a child. Studies of a kindred.
    Monteleone JA, Beutler E, Monteleone PL, Utz CL, Casey EC.
    Am J Med; 1971 Mar 27; 50(3):403-7. PubMed ID: 5553957
    [No Abstract] [Full Text] [Related]

  • 11. [Galactose intolerance in a newborn infant].
    Hessel D, Zöllner H, Türk E.
    Kinderarztl Prax; 1967 Jun 27; 35(6):263-7. PubMed ID: 5602226
    [No Abstract] [Full Text] [Related]

  • 12. Maternal enzymes of galactose metabolism and the "inexplicable" infantile cataract.
    Harley JD, Mutton P, Irvine S, Gupta JD.
    Lancet; 1974 Aug 03; 2(7875):259-61. PubMed ID: 4136146
    [No Abstract] [Full Text] [Related]

  • 13. Galactose and glucose metabolism in galactokinase deficient, galactose-1-P-uridyl transferase deficient and normal human fibroblasts.
    Friedman TB, Yarkin RJ, Merril CR.
    J Cell Physiol; 1975 Jun 03; 85(3):569-78. PubMed ID: 167035
    [Abstract] [Full Text] [Related]

  • 14. [Galactosemia: a hereditary galactose intolerance].
    Sychlowy A.
    Pediatr Pol; 1972 Jul 03; 47(7):901-6. PubMed ID: 4559957
    [No Abstract] [Full Text] [Related]

  • 15. Clinical features of galactokinase deficiency: a review of the literature.
    Bosch AM, Bakker HD, van Gennip AH, van Kempen JV, Wanders RJ, Wijburg FA.
    J Inherit Metab Dis; 2002 Dec 03; 25(8):629-34. PubMed ID: 12705493
    [Abstract] [Full Text] [Related]

  • 16. Cataracts related to enzymes of galactose metabolism.
    Schoon DV.
    Metab Pediatr Ophthalmol; 1981 Dec 03; 5(3-4):219-23. PubMed ID: 6273670
    [No Abstract] [Full Text] [Related]

  • 17. A patient with hereditary galactokinase deficiency.
    Dahlqvist A, Gamstorp I, Madsen H.
    Acta Paediatr Scand; 1970 Nov 03; 59(6):669-75. PubMed ID: 5482251
    [No Abstract] [Full Text] [Related]

  • 18. [Partial and transitory erythrocyte galactokinase deficiency in a newborn. Biochemical study].
    Vigneron C, Marchal C, Deifts C, Vidailhet M, Pierson M, Neimann N.
    Arch Fr Pediatr; 1970 May 03; 27(5):523-31. PubMed ID: 5425825
    [No Abstract] [Full Text] [Related]

  • 19. Disorders of galactose metabolism.
    Rennert OM.
    Ann Clin Lab Sci; 1977 May 03; 7(6):443-8. PubMed ID: 931348
    [Abstract] [Full Text] [Related]

  • 20. [Congenital enzyme deficiency in carbohydrate metabolism. Its significance for clinical pediatrics and human biochemical genetics (author's transl)].
    Schaub J, Osang M.
    MMW Munch Med Wochenschr; 1976 May 07; 118(19):609-14. PubMed ID: 180406
    [Abstract] [Full Text] [Related]

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