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Journal Abstract Search

274 related items for PubMed ID: 6273670

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

  • 2. [Double heterozygosity (transferase-/epimerase-defect) and galactosemia cataract].
    Heyne K, Shin YS, Schwinger E.
    Monatsschr Kinderheilkd; 1988 Dec; 136(12):828-30. PubMed ID: 2853298
    [Abstract] [Full Text] [Related]

  • 3. [Identification of inborn errors of galactose metabolism in patients with cataracts].
    Vaca-Pacheco G, Medina C, García-Cruz D, Sánchez-Corona J, Chávez-Anaya E, Jaimes C, Hernández-Córdova A.
    Arch Invest Med (Mex); 1990 Dec; 21(2):127-32. PubMed ID: 2103700
    [Abstract] [Full Text] [Related]

  • 4. Laboratory screening in the assessment of human cataract.
    Winder AF.
    Trans Ophthalmol Soc U K (1962); 1981 Dec; 101(1):127-30. PubMed ID: 6964219
    [Abstract] [Full Text] [Related]

  • 5. Galactosaemia and the problem of galactose toxicity.
    Schwarz V.
    Biochem Soc Trans; 1975 Dec; 3(2):234-8. PubMed ID: 165990
    [No Abstract] [Full Text] [Related]

  • 6. [Galactokinase deficiency].
    Colin J, Voyer M, Thomas D, Charlas J.
    Ann Pediatr (Paris); 1976 May 02; 23(5):371-7. PubMed ID: 16104211
    [No Abstract] [Full Text] [Related]

  • 7. Galactose and cataract.
    Stambolian D.
    Surv Ophthalmol; 1988 May 02; 32(5):333-49. PubMed ID: 3043741
    [Abstract] [Full Text] [Related]

  • 8. [The frequency of uridyl transferase deficiency in patients with galactose intolerance].
    Fernekorn A, Fiehring C.
    Dtsch Gesundheitsw; 1976 Dec 04; 31(52):2455-60. PubMed ID: 1009846
    [No Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. [Pathological findings in galactosemia caused by a galactose-1-phosphaturidyltransferase defect (author's transl)].
    Gathmann HA.
    Klin Padiatr; 1977 Mar 07; 189(2):177-84. PubMed ID: 558474
    [Abstract] [Full Text] [Related]

  • 11. [Tests for galactose metabolism].
    Ohya N.
    Nihon Rinsho; 1997 Mar 07; 55 Suppl 1():244-7. PubMed ID: 9097598
    [No Abstract] [Full Text] [Related]

  • 12. Galactose intolerance and the risk of cataract.
    Winder AF, Fells P, Jones RB, Kissun RD, Menzies IS, Mount JN.
    Br J Ophthalmol; 1982 Jul 07; 66(7):438-41. PubMed ID: 7093182
    [Abstract] [Full Text] [Related]

  • 13. A case of cataract formation during the lactating period associated with galactose-1-phosphate uridyl transferase deficiency.
    Avisar RA, Schwartzman S, Levinsky H, Allalouf D, Goldman J, Ninio A, Savir H.
    Metab Pediatr Syst Ophthalmol; 1982 Jul 07; 6(1):45-8. PubMed ID: 6290834
    [No Abstract] [Full Text] [Related]

  • 14. Partial galactose disorders in families with premature cataracts.
    Winder AF, Claringbold LJ, Jones RB, Jay BS, Rice NS, Kissun RD, Menzies IS, Mount JN.
    Arch Dis Child; 1983 May 07; 58(5):362-6. PubMed ID: 6859916
    [Abstract] [Full Text] [Related]

  • 15. Presenile cataract formation and decreased activity of galactosemic enzymes.
    Skalka HW, Prchal JT.
    Arch Ophthalmol; 1980 Feb 07; 98(2):269-73. PubMed ID: 7352874
    [Abstract] [Full Text] [Related]

  • 16. Molecular basis of disorders of human galactose metabolism: past, present, and future.
    Novelli G, Reichardt JK.
    Mol Genet Metab; 2000 Feb 07; 71(1-2):62-5. PubMed ID: 11001796
    [Abstract] [Full Text] [Related]

  • 17. [Screening of newborns for inborn errors of galactose metabolism. Methods and results].
    Gitzelmann R.
    Monatsschr Kinderheilkd (1902); 1976 Sep 07; 129(9):654-7. PubMed ID: 185513
    [Abstract] [Full Text] [Related]

  • 18. Direct and maternal aspects of the risk of cataract with partial disorders of galactose metabolism.
    Winder AF, Fielder AR, Mount JN, Menzies JS.
    Clin Genet; 1985 Sep 07; 28(3):199-206. PubMed ID: 4064358
    [Abstract] [Full Text] [Related]

  • 19. Possible role of galactose-1-P-uridyl transferase activity deficiency in red blood cells in the development of the presenile and senile cataract.
    Simonelli F, De Rosa G, Rinaldi E, Auricchio L.
    Ophthalmic Res; 1986 Sep 07; 18(5):309-12. PubMed ID: 3027641
    [Abstract] [Full Text] [Related]

  • 20. [Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)].
    Brivet M, Moatti N, Lemonnier A.
    Ann Biol Clin (Paris); 1979 Sep 07; 37(5):259-70. PubMed ID: 232826
    [Abstract] [Full Text] [Related]

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