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PUBMED FOR HANDHELDS

Journal Abstract Search


185 related items for PubMed ID: 165990

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

  • 2. Biokinetics of galactose in the homozygotes and heterozygotes of both forms of galactosemia.
    Sitzmann FC, Kaloud H.
    Clin Chim Acta; 1976 Nov 01; 72(3):343-51. PubMed ID: 184990
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  • 3. Cataracts related to enzymes of galactose metabolism.
    Schoon DV.
    Metab Pediatr Ophthalmol; 1981 Nov 01; 5(3-4):219-23. PubMed ID: 6273670
    [No Abstract] [Full Text] [Related]

  • 4. [Double heterozygosity (transferase-/epimerase-defect) and galactosemia cataract].
    Heyne K, Shin YS, Schwinger E.
    Monatsschr Kinderheilkd; 1988 Dec 01; 136(12):828-30. PubMed ID: 2853298
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  • 5. Duarte variant-galactosemia heterozygote. Repository identification No. GM-1996.
    Donnell GN, Ng WG, Alfi OS, Greene AE, Coriell LL.
    Cytogenet Cell Genet; 1977 Dec 01; 19(1):53-4. PubMed ID: 891264
    [No Abstract] [Full Text] [Related]

  • 6. Hormonal status of galactosaemia homozygotes.
    Coulam CB.
    Lancet; 1981 Jan 17; 1(8212):165. PubMed ID: 6109851
    [No Abstract] [Full Text] [Related]

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  • 10. Prenatal diagnosis of galactosaemia in six pregnancies -- possible complications with rare alleles of the galactose 1-phosphate uridyl transferase locus.
    Benson PF, Brandt NJ, Christensen E, Fensom AH.
    Clin Genet; 1979 Nov 17; 16(5):311-6. PubMed ID: 519903
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  • 17. Evaluation of reduced activity galactose-1-phosphate uridyl transferase by combined radioisotopic assay and high-resolution isoelectric focusing.
    Kelley RI, Segal S.
    J Lab Clin Med; 1989 Aug 17; 114(2):152-6. PubMed ID: 2546999
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  • 18. GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE ASSAY BY USE OF RADIOACTIVE GALACTOSE-1-PHOSPHATE.
    NG WG, BERGEN WR, DONNELL GN.
    Clin Chim Acta; 1964 Oct 17; 10():337-43. PubMed ID: 14219578
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  • 19. Galactose-1-phosphate uridyl transferase deficiency due to Duarte/galactosemia combined variation: clinical and biochemical studies.
    Levy HL, Sepe SJ, Walton DS, Shih VE, Hammersen G, Houghton S, Beutler E.
    J Pediatr; 1978 Mar 17; 92(3):390-3. PubMed ID: 632977
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