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Journal Abstract Search


175 related items for PubMed ID: 1612673

  • 1. Spectrum of neonatal hyperbilirubinemia: an analysis of 454 cases.
    Singhal PK, Singh M, Paul VK, Deorari AK, Ghorpade MG.
    Indian Pediatr; 1992 Mar; 29(3):319-25. PubMed ID: 1612673
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  • 2. Intravenous immunoglobulin G (IVIG) therapy for significant hyperbilirubinemia in ABO hemolytic disease of the newborn.
    Miqdad AM, Abdelbasit OB, Shaheed MM, Seidahmed MZ, Abomelha AM, Arcala OP.
    J Matern Fetal Neonatal Med; 2004 Sep; 16(3):163-6. PubMed ID: 15590442
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  • 3. Exchange transfusion in neonatal hyperbilirubinemia.
    Dikshit SK, Gupta PK.
    Indian Pediatr; 1989 Nov; 26(11):1139-45. PubMed ID: 2630476
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  • 4. Intravenous immunoglobulin in ABO and Rh hemolytic diseases of newborn.
    Nasseri F, Mamouri GA, Babaei H.
    Saudi Med J; 2006 Dec; 27(12):1827-30. PubMed ID: 17143357
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  • 5. 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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  • 7. [Neonatal ABO incompatibility underlies a potentially severe hemolytic disease of the newborn and requires adequate care].
    Senterre T, Minon JM, Rigo J.
    Arch Pediatr; 2011 Mar; 18(3):279-82. PubMed ID: 21255989
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  • 9. [Current validity of the exchange transfusion intervention by the classic indication. Our 15 years' experience].
    Zuppa AA, Vento G, Tornesello A, Papacci P, Micanti M, Coviello C, Palusci A, Mazzotta M, Fundarò C, Romagnoli C.
    Minerva Pediatr; 1990 Apr; 42(4):135-41. PubMed ID: 2115969
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  • 10. Exchange transfusion in newborn infants with perinatal hemolytic disease. Efficacy of the procedure.
    Ceccon ME, Diniz EM, Ramos JL, Vaz FA.
    Rev Paul Med; 1993 Apr; 111(2):348-53. PubMed ID: 8284577
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  • 12. [Perinatal management and neurological outcome of newborns hospitalized with Rhesus hemolytic disease].
    Gobalakichenane P, Lardennois C, Galène-Gromez S, Brossard V, Marpeau L, Verspyck E, Marret S, le Réseau de périnatalité de Haute-Normandie.
    Gynecol Obstet Fertil; 2008 Oct; 36(10):984-90. PubMed ID: 18804397
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  • 13. Hemolytic disease of the newborn caused by irregular blood subgroup (Kell, C, c, E, and e) incompatibilities: report of 106 cases at a tertiary-care centre.
    Karagol BS, Zenciroglu A, Okumus N, Karadag N, Dursun A, Hakan N.
    Am J Perinatol; 2012 Jun; 29(6):449-54. PubMed ID: 22399212
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  • 14. Sn-Mesoporphyrin interdiction of severe hyperbilirubinemia in Jehovah's Witness newborns as an alternative to exchange transfusion.
    Kappas A, Drummond GS, Munson DP, Marshall JR.
    Pediatrics; 2001 Dec; 108(6):1374-7. PubMed ID: 11731664
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  • 15. [Clinico-statistical considerations on newborn infants treated with exchange transfusions for hemolytic disease caused by Rh isoimmunization or ABO incompatibility and for hyperbilirubinemia of non-immunological causes in full-term newborn infant. (Examination of 462 cases)].
    Di Piero G, Mencarini L, Ottaviano S, Lapi AS.
    Riv Clin Pediatr; 1967 Dec; 80(4):89-112. PubMed ID: 4974851
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  • 16. Glucose-6-phosphate dehydrogenase deficiency in the newborn: its prevalence and relation to neonatal jaundice.
    Tanphaichitr VS, Pung-amritt P, Yodthong S, Soongswang J, Mahasandana C, Suvatte V.
    Southeast Asian J Trop Med Public Health; 1995 Dec; 26 Suppl 1():137-41. PubMed ID: 8629093
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  • 18. Genetic interactions in the pathogenesis of neonatal hyperbilirubinemia: Gilbert's Syndrome and glucose-6-phosphate dehydrogenase deficiency.
    Kaplan M.
    J Perinatol; 2001 Dec; 21 Suppl 1():S30-4; discussion S35-9. PubMed ID: 11803413
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