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Journal Abstract Search

195 related items for PubMed ID: 8490627

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  • 6. [Favism in Polish families].
    Jabłońska-Skwiecińska E, Pogłód R, Skrobowska A.
    Pol Tyg Lek; ; 45(38-39):778-81. PubMed ID: 2095545
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  • 7. Identification of Mediterranean mutation in Egyptian favism patients.
    Osman HG, Zahran FM, El-Sokkary AM, El-Said A, Sabry AM.
    Eur Rev Med Pharmacol Sci; 2014 Oct; 18(19):2821-7. PubMed ID: 25339475
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  • 8. G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotype.
    Cappellini MD, Sampietro M, Toniolo D, Carandina G, Martinez di Montemuros F, Tavazzi D, Fiorelli G.
    Hum Genet; 1994 Feb; 93(2):139-42. PubMed ID: 7906668
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  • 9. Glucose-6-phosphate dehydrogenase variants associated with favism in Thai children.
    Laosombat V, Sattayasevana B, Chotsampancharoen T, Wongchanchailert M.
    Int J Hematol; 2006 Feb; 83(2):139-43. PubMed ID: 16513531
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  • 10. Molecular genetics of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain: identification of two new point mutations in the G6PD gene.
    Rovira A, Vulliamy T, Pujades MA, Luzzatto L, Corrons JL.
    Br J Haematol; 1995 Sep; 91(1):66-71. PubMed ID: 7577654
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  • 11. Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia.
    Vulliamy TJ, D'Urso M, Battistuzzi G, Estrada M, Foulkes NS, Martini G, Calabro V, Poggi V, Giordano R, Town M.
    Proc Natl Acad Sci U S A; 1988 Jul; 85(14):5171-5. PubMed ID: 3393536
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  • 13. Family investigations of erythrocyte glucose-6-phosphate dehydrogenase in favism.
    Rozynkowa D, Gebala A, Zagórski Z.
    Pol Med J; 1970 Jul; 9(5):1093-9. PubMed ID: 5510280
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  • 15. Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Tunisia.
    Daoud BB, Mosbehi I, Préhu C, Chaouachi D, Hafsia R, Abbes S.
    Pathol Biol (Paris); 2008 Jul; 56(5):260-7. PubMed ID: 18226470
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  • 16. [Molecular analysis of glucose-6-dehydrogenase deficiency in Spain].
    Vives Corrons JL, Zarza R, Aymerich JM, Boixadera J, Carrera A, Colomer D, Corbella M, Castro M, Crespo JM, Del Arco A, Erkiaga S, Font L, González I, Juncá J, Lausin A, Manrubia E, Martín Núñez G, Murga MJ, Oliva E, Pérez de Mendiguren B, Pujades MA, Remacha A, Rovira A, Villegas A.
    Sangre (Barc); 1997 Oct; 42(5):391-8. PubMed ID: 9424740
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  • 17. Molecular heterogeneity underlying the G6PD Mediterranean phenotype.
    Corcoran CM, Calabrò V, Tamagnini G, Town M, Haidar B, Vulliamy TJ, Mason PJ, Luzzatto L.
    Hum Genet; 1992 Mar; 88(6):688-90. PubMed ID: 1551674
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  • 18. Glucose-6-phosphate dehydrogenase (G6PD) deficiency in southern Italy: a case of G6PD A(-) associated with favism.
    Calabrò V, Cascone A, Malaspina P, Battistuzzi G.
    Haematologica; 1989 Mar; 74(1):71-3. PubMed ID: 2498187
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  • 19. Neonatal jaundice in Saudi newborns with G6PD Aures.
    Niazi GA, Adeyokunnu A, Westwood B, Beutler E.
    Ann Trop Paediatr; 1996 Mar; 16(1):33-7. PubMed ID: 8787363
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