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Journal Abstract Search


302 related items for PubMed ID: 18379570

  • 1. Severe hemolysis with normal blood count in a glucose-6-phosphate dehydrogenase deficient neonate.
    Kaplan M, Hammerman C, Vreman HJ, Wong RJ, Stevenson DK.
    J Perinatol; 2008 Apr; 28(4):306-9. PubMed ID: 18379570
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  • 2. Donor blood glucose 6-phosphate dehydrogenase deficiency reduces the efficacy of exchange transfusion in neonatal hyperbilirubinemia.
    Samanta S, Kumar P, Kishore SS, Garewal G, Narang A.
    Pediatrics; 2009 Jan; 123(1):e96-e100. PubMed ID: 19103674
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  • 3. Severe hyperbilirubinemia in a glucose-6-phosphate dehydrogenase-deficient preterm neonate: could prematurity be the main responsible factor?
    Costa S, De Carolis MP, De Luca D, Savarese I, Romagnoli C.
    Fetal Diagn Ther; 2008 Jan; 24(4):440-3. PubMed ID: 19023210
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  • 5. Neonatal hyperbilirubinemia associated with glucose-6-phosphate dehydrogenase deficiency in Sephardic-Jewish neonates: incidence, severity, and the effect of phototherapy.
    Kaplan M, Abramov A.
    Pediatrics; 1992 Sep; 90(3):401-5. PubMed ID: 1518696
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  • 8. Bilirubin conjugation, reflected by conjugated bilirubin fractions, in glucose-6-phosphate dehydrogenase-deficient neonates: a determining factor in the pathogenesis of hyperbilirubinemia.
    Kaplan M, Muraca M, Hammerman C, Vilei MT, Leiter C, Rudensky B, Rubaltelli FF.
    Pediatrics; 1998 Sep; 102(3):E37. PubMed ID: 9724685
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  • 9. G6PD-deficient donor blood as a cause of hemolysis in two preterm infants.
    Mimouni F, Shohat S, Reisner SH.
    Isr J Med Sci; 1986 Feb; 22(2):120-2. PubMed ID: 3949489
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  • 11. Glucose-6-phosphate dehydrogenase deficiency and Gilbert syndrome: a gene interaction underlies severe jaundice without severe hemolysis.
    Nicolaidou P, Kostaridou S, Mavri A, Galla A, Kitsiou S, Stamoulakatou A.
    Pediatr Hematol Oncol; 2005 Feb; 22(7):561-6. PubMed ID: 16166048
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  • 12. Implementation and analysis of a pilot in-hospital newborn screening program for glucose-6-phosphate dehydrogenase deficiency in the United States.
    Nock ML, Johnson EM, Krugman RR, Di Fiore JM, Fitzgerald S, Sandhaus LM, Walsh MC.
    J Perinatol; 2011 Feb; 31(2):112-7. PubMed ID: 20539275
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  • 14. Massive acute haemolysis and severe neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient preterm triplets.
    Shah VA, Yeo CL.
    J Paediatr Child Health; 2007 May; 43(5):411-3. PubMed ID: 17489836
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  • 17. Failure to predict hemolysis and hyperbilirubinemia by IgG subclass in blood group A or B infants born to group O mothers.
    Kaplan M, Na'amad M, Kenan A, Rudensky B, Hammerman C, Vreman HJ, Wong RJ, Stevenson DK.
    Pediatrics; 2009 Jan; 123(1):e132-7. PubMed ID: 19114458
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  • 18. Is it accurate to separate glucose-6-phosphate dehydrogenase activity in neonatal hyperbilirubinemia as deficient and normal?
    Kilicdag H, Gökmen Z, Ozkiraz S, Gulcan H, Tarcan A.
    Pediatr Neonatol; 2014 Jun; 55(3):202-7. PubMed ID: 24326153
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  • 19. (TA)n UGT 1A1 promoter polymorphism: a crucial factor in the pathophysiology of jaundice in G-6-PD deficient neonates.
    Kaplan M, Renbaum P, Vreman HJ, Wong RJ, Levy-Lahad E, Hammerman C, Stevenson DK.
    Pediatr Res; 2007 Jun; 61(6):727-31. PubMed ID: 17426648
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  • 20. Glucose-6-phosphate dehydrogenase deficiency in ethnic minorities in The Netherlands.
    Wolf BH, Schutgens RB, Nagelkerke NJ, Weening RS.
    Trop Geogr Med; 1988 Oct; 40(4):322-30. PubMed ID: 3227552
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