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Journal Abstract Search

117 related items for PubMed ID: 3038378

  • 1. Reagent that restores galactose-1-phosphate uridylyltransferase activity in dry blood spots.
    Berry HK, Croft CC.
    Clin Chem; 1987 Aug; 33(8):1471-2. PubMed ID: 3038378
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  • 2. A screening procedure and a specific quantitative method for UDPglucose: alpha-D-galactose-1-phosphate uridylyltransferase (EC 2.7.7.12).
    Ibbott FA.
    Clin Chem; 1977 Jul; 23(7):1348-55. PubMed ID: 872388
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  • 4. [Galactose 1-phosphate level in children with various types of hexosephosphate uridylyltransferase deficiency].
    Grodzka Z, Zbieg-Sendecka E, Mańkowski T.
    Pediatr Pol; 1985 Sep; 60(9):631-7. PubMed ID: 3008074
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  • 5. Pitfalls in the radioactive method of galactose-1-phosphate uridyltransferase activity measurement.
    Shin-Buehring YS, Schaub J.
    Clin Chim Acta; 1980 Sep 25; 106(2):231-4. PubMed ID: 6250747
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  • 7. [Enzymatic analysis for the diagnosis of inborn errors of carbohydrate metabolism].
    Kusunoki T, Soyama K, Oya N, Kinugasa A.
    Nihon Rinsho; 1979 Jun 29; Suppl():1619-23. PubMed ID: 290838
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  • 10. Biochemical studies of a human low-activity galactose-1-phosphate uridyl transferase variant.
    Ng WG, Kline F, Lin J, Koch R, Donnell GN.
    J Inherit Metab Dis; 1978 Jun 29; 1(4):145-51. PubMed ID: 117249
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  • 11. Human red cell galactose-1-phosphate uridylyltransferase (EC 2.7.7.12). Electrophoretically determined polymorphism in Denmark and its use in paternity cases.
    Eriksen B, Dissing J.
    Hum Hered; 1980 Jun 29; 30(1):27-32. PubMed ID: 6243609
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  • 12. Purification and characterization of human erythrocyte uridylyl transferase.
    Banroques J, Gregori C, Schapira F.
    Biochim Biophys Acta; 1981 Feb 13; 657(2):374-82. PubMed ID: 6260202
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  • 15. GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE ACTIVITY IN GALACTOSAEMIA.
    WONGIN NG, BERGREN WR, DONNELL GN.
    Nature; 1964 Aug 22; 203():845-7. PubMed ID: 14204065
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  • 18. [Clinical and biochemical diagnosis of galactosemia among our cases].
    Bozkowa K, Zbieg-Sendecka E, Grodzka Z, Cabalska B.
    Probl Med Wieku Rozwoj; 1979 Aug 22; 8():63-9. PubMed ID: 263527
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  • 19. Development of a protocol for newborn screening for disorders of the galactose metabolic pathway.
    Bowling FG, Brown AR.
    J Inherit Metab Dis; 1986 Aug 22; 9(1):99-104. PubMed ID: 3014213
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  • 20. Inexplicable infantile cataracts and partial maternal galactose disorder.
    Brivet M, Abadie V, Soni T, Cheron G, Dufier JL.
    Arch Dis Child; 1986 May 22; 61(5):445-8. PubMed ID: 3013103
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