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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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related] Page: [Next] [New Search]