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Journal Abstract Search

100 related items for PubMed ID: 6452554

  • 1. [Hypergalactosemia in newborns as uncovered by the Austrian screening program in 12 years (author's transl)].
    Thalhammer O, Scheibenreiter S, Knoll E, Wehle E.
    Klin Padiatr; 1980 Nov; 192(6):613-9. PubMed ID: 6452554
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  • 4. [Pathological findings in galactosemia caused by a galactose-1-phosphaturidyltransferase defect (author's transl)].
    Gathmann HA.
    Klin Padiatr; 1977 Mar; 189(2):177-84. PubMed ID: 558474
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  • 5. [Ophthalmologic follow-up examination in galactosemia (author's transl)].
    Zehetbauer G, Scheibenreiter S.
    Klin Padiatr; 1977 Nov; 189(6):451-4. PubMed ID: 563943
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  • 6. [Screening for galactose-1-phosphate uridyltransferase deficiency (classic galactosemia) in newborns].
    Ahlbehrendt I, Wagenknecht C.
    Acta Biol Med Ger; 1977 Nov; 36(5-6):797-800. PubMed ID: 602584
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  • 7. [Clinical and biochemical diagnosis of galactosemia among our cases].
    Bozkowa K, Zbieg-Sendecka E, Grodzka Z, Cabalska B.
    Probl Med Wieku Rozwoj; 1979 Nov; 8():63-9. PubMed ID: 263527
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  • 8. Screening for galactosemia: Philippines experience. Newborn Screening Study Group.
    Lee JY, Padilla CD, Chua EL.
    Southeast Asian J Trop Med Public Health; 1999 Nov; 30 Suppl 2():66-8. PubMed ID: 11405207
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  • 9. Galactosemia as a result of galactose-1-phosphate uridyltransferase deficiency.
    Vaca G, Sanchez-Corona J, Medina C, Olivares N, Rivera H, Hernández A, Ibarra B, Sotomayor JM, Cantú JM.
    Arch Invest Med (Mex); 1978 Nov; 9(3):477-84. PubMed ID: 568459
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  • 10. [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
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  • 11. An unexpectedly high frequency of hypergalactosemia in an immigrant Bosnian population revealed by newborn screening.
    Reich S, Hennermann J, Vetter B, Neumann LM, Shin YS, Söling A, Mönch E, Kulozik AE.
    Pediatr Res; 2002 May; 51(5):598-601. PubMed ID: 11978883
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  • 13. [Long-term results in children with classical galactosemia].
    Scheibenreiter S, Knoll E, Widhalm K.
    Wien Klin Wochenschr; 1992 May; 104(16):514-7. PubMed ID: 1413810
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  • 17. Curious neurologic sequelae in galactosemia.
    Lo W, Packman S, Nash S, Schmidt K, Ireland S, Diamond I, Ng W, Donnell G.
    Pediatrics; 1984 Mar; 73(3):309-12. PubMed ID: 6701054
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  • 19. [Screening of newborns for inborn errors of galactose metabolism. Methods and results].
    Gitzelmann R.
    Monatsschr Kinderheilkd (1902); 1976 Sep; 129(9):654-7. PubMed ID: 185513
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