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Journal Abstract Search

78 related items for PubMed ID: 132644

  • 1. [Neo-natal hyperbilirubinemia and G-6-PD Ankara deficiency, a new enzymatic variant discovered in a Turkish family (author's transl)].
    North ML, Kahn A, Messer KJ, Willard D, Boivin P.
    Nouv Rev Fr Hematol; 1975; 15(4):454-9. PubMed ID: 132644
    [Abstract] [Full Text] [Related]

  • 2. [Deficiency of red cell glucose-6-phosphate-dehydrogenase due to a slow variant in a French family. Relationship with the Gd (-) Seattle variant (author's transl)].
    Kahn A, Boivin P, Lagneau J, Cruveiller J.
    Nouv Rev Fr Hematol; 1973; 13(2):163-71. PubMed ID: 4270706
    [No Abstract] [Full Text] [Related]

  • 3. A glucose 6-phosphate dehydrogenase Gd (-) Castilla variant characterized by mild deficiency associated with drug-induced hemolytic anemia.
    Lisker R, Briceno RP, Zavala C, Navarrette JI, Wessels M, Yoshida A.
    J Lab Clin Med; 1977 Oct; 90(4):754-9. PubMed ID: 903703
    [Abstract] [Full Text] [Related]

  • 4. G-6PD "ankara". a new G-6PD variant with deficiency found in a Turkish family.
    Kahn A, North ML, Messer J, Boivin P.
    Humangenetik; 1975 Oct; 27(3):247-50. PubMed ID: 1150245
    [Abstract] [Full Text] [Related]

  • 5. Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency in Switzerland. Demonstration of a new variant (G-6-PD Aarau) with chronic nonsphaerocytic haemolytic anaemia.
    Gahr M, Schröter W, Sturzenegger M, Bornhalm D, Marti HR.
    Helv Paediatr Acta; 1976 Aug; 31(2):159-66. PubMed ID: 955939
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Frequency and origin of G-6-PD deficiency among icteric newborns in the metropolitan area of Monterrey, Nuevo León, Mexico.
    González-Quiroga G, Ramirez-Del Rio JL, Cerda-Flores RM, Garza-Chapa R.
    Gene Geogr; 1994 Dec; 8(3):157-64. PubMed ID: 7662606
    [Abstract] [Full Text] [Related]

  • 8. 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 Dec; 24(4):440-3. PubMed ID: 19023210
    [Abstract] [Full Text] [Related]

  • 9. Glucose-6-phosphate dehydrogenase deficiency and hyperbilirubinemia in the newborn.
    Lopez R, Cooperman JM.
    Med Chir Dig; 1973 Dec; 2(2):111-7. PubMed ID: 4743207
    [No Abstract] [Full Text] [Related]

  • 10. [Glucose-6-phosphate dehydrogenase deficiency of the mediterranean type B minus. 2. Etiological basis for severe hyperbilirubinemia in the newborn].
    Schulz D, Rothenhöfer C.
    Fortschr Med; 1978 Mar 23; 96(11):565-70. PubMed ID: 631693
    [Abstract] [Full Text] [Related]

  • 11. [A family of new glucose 6-phosphate dehydrogenase (G 6 PD) variant associated with chronic nonspherocytic hemolytic anemia: G 6 PD Kurume (author's transl)].
    Kaneto A, Motokawa M, Koga T, Shimokawa Y, Tanikawa K, Fujii H, Miwa S.
    Rinsho Ketsueki; 1979 Jan 23; 20(1):82-9. PubMed ID: 423378
    [No Abstract] [Full Text] [Related]

  • 12. Neonatal hyperbilirubinemia and glucose-6-phosphate dehydrogenase deficiency.
    Milbauer B, Peled N, Svirsky S.
    Isr J Med Sci; 1973 Jan 23; 9(11):1547-52. PubMed ID: 4778402
    [No Abstract] [Full Text] [Related]

  • 13. Combined glucose phosphate isomerase and glucose-6-phosphate dehydrogenase deficiency of erythrocytes.
    Steiman I, Kaufman S, Zaidman JL, Leiba H.
    Isr J Med Sci; 1978 Nov 23; 14(11):1186-90. PubMed ID: 750548
    [Abstract] [Full Text] [Related]

  • 14. Cord plasma alpha-fetoprotein values and neonatal jaundice.
    Tan KL, Loganath A, Roy AC, Goh HH, Karim SM, Ratnam SS.
    Pediatrics; 1984 Dec 23; 74(6):1065-8. PubMed ID: 6209608
    [Abstract] [Full Text] [Related]

  • 15. [Clinical studies on glucose-6-phosphate dehydrogenase activity in neonatal hyperbilirubinemia].
    Takahashi H.
    Igaku Kenkyu; 1970 Feb 23; 40(1):105-15. PubMed ID: 5463372
    [No Abstract] [Full Text] [Related]

  • 16. [Various genetic and clinical aspects of patients with hemolytic anemia caused by glucosephosphate dehydrogenase deficiency (DG6F)].
    Toro AH, Soto Allande R, Bello González A.
    Bol Med Hosp Infant Mex; 1975 Feb 23; 32(2):211-25. PubMed ID: 1138706
    [Abstract] [Full Text] [Related]

  • 17. Effect of phenobarbital treatment on erythrocyte glucose-6-phosphate dehydrogenase in human newborns.
    Laconi E, Dessì S, Batetta B, Pani P, Pirisi L, Andria C, Macciotta A.
    Pediatr Pharmacol (New York); 1983 Feb 23; 3(2):59-62. PubMed ID: 6674910
    [Abstract] [Full Text] [Related]

  • 18. [Postoperative haemolytic jaundice due to deficiency of G-6-PD (author's transl)].
    Tschen HH, Michot F, Villiger KJ.
    Zentralbl Chir; 1977 Feb 23; 102(20):1266-9. PubMed ID: 595942
    [Abstract] [Full Text] [Related]

  • 19. [Frequency and complications of erythrocyte glucose-6-phosphate dehydrogenase deficiency in the African newborn in Dakar. Preliminary study].
    Tchernia G, Zucker JM, Oudart JL, Boal MR, Kuakuvi N.
    Nouv Rev Fr Hematol; 1971 Feb 23; 11(1):145-57. PubMed ID: 4252101
    [No Abstract] [Full Text] [Related]

  • 20. Heterozygous erythrocyte glutathione peroxidase deficiency associated with neonatal hyperbilirubinemia found in a Japanese family.
    Miwa S, Nakashima K, Ariyoshi K, Uemura M, Murashima N.
    Nihon Ketsueki Gakkai Zasshi; 1974 Jun 23; 37(3):266-70. PubMed ID: 4479916
    [No Abstract] [Full Text] [Related]

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