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PUBMED FOR HANDHELDS

Journal Abstract Search

123 related items for PubMed ID: 872388

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  • 3. 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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  • 5. [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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  • 9. Human erythrocyte galactose-1-phosphate uridylyltransferase. Evidence for a uridylyl-enzyme intermediate by kinetic and exchange reaction studies.
    Markus HB, Wu JW, Boches FS, Tedesco TA, Mellman WJ, Kallen RG.
    J Biol Chem; 1977 Aug 10; 252(15):5363-9. PubMed ID: 889611
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  • 10. 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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  • 13. [Organization of a screening program for congenital metabolic disorders in newborn infants in Berlin--problems, results and experiences. 1. Screening tests for classical galactosemia].
    Ahlbehrendt I, Wagenknecht C.
    Z Med Lab Diagn; 1977 Dec 22; 18(6):350-5. PubMed ID: 607656
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  • 19. [Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)].
    Brivet M, Moatti N, Lemonnier A.
    Ann Biol Clin (Paris); 1979 Dec 22; 37(5):259-70. PubMed ID: 232826
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