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


141 related items for PubMed ID: 6859916

  • 1. 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; 58(5):362-6. PubMed ID: 6859916
    [Abstract] [Full Text] [Related]

  • 2. 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; 28(3):199-206. PubMed ID: 4064358
    [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 Sep; 21(2):127-32. PubMed ID: 2103700
    [Abstract] [Full Text] [Related]

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

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

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. 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 Jul; 18(5):309-12. PubMed ID: 3027641
    [Abstract] [Full Text] [Related]

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

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

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. [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]

  • 16. Galactose disorders: an overview.
    Holton JB.
    J Inherit Metab Dis; 1990 Dec; 13(4):476-86. PubMed ID: 2122114
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 20. Elevated plasma galactitol levels in patients with congenital cataracts without apparent enzyme defect.
    Jakobs C, Douwes AC, Kok R, de Jong A, Endres W, Shin YS.
    Eur J Pediatr; 1988 May; 147(4):446. PubMed ID: 3396605
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 8.