BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 8490627)

  • 1. G6PD Aures: a new mutation (48 Ile-->Thr) causing mild G6PD deficiency is associated with favism.
    Nafa K; Reghis A; Osmani N; Baghli L; Benabadji M; Kaplan JC; Vulliamy TJ; Luzzatto L
    Hum Mol Genet; 1993 Jan; 2(1):81-2. PubMed ID: 8490627
    [No Abstract]   [Full Text] [Related]  

  • 2. Favism in GdMediterranean heterozygous females.
    Sanna G; De Virgiliis S; Palmas C; Argiolu F; Frau F; Cao A
    Pediatr Res; 1979 Jul; 13(7):812-6. PubMed ID: 481952
    [No Abstract]   [Full Text] [Related]  

  • 3. Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism.
    Jablonska-Skwiecinska E; Lewandowska I; Plochocka D; Topczewski J; Zimowski JG; Klopocka J; Burzynska B
    Hum Mutat; 1999; 14(6):477-84. PubMed ID: 10571945
    [TBL] [Abstract][Full Text] [Related]  

  • 4. At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria.
    Nafa K; Reghis A; Osmani N; Baghli L; Aït-Abbes H; Benabadji M; Kaplan JC; Vulliamy T; Luzzatto L
    Hum Genet; 1994 Nov; 94(5):513-7. PubMed ID: 7959686
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Favism - a familial enzymatic defect of the red blood cells in a 7-year-old girl].
    Pohorecka J; Jabłońska-Skwiecińska E; Powiertowska-Ryszka G
    Pediatr Pol; 1982; 57(9):731-4. PubMed ID: 7170153
    [No Abstract]   [Full Text] [Related]  

  • 6. [Favism in Polish families].
    Jabłońska-Skwiecińska E; Pogłód R; Skrobowska A
    Pol Tyg Lek; 1990 Sep 17-24; 45(38-39):778-81. PubMed ID: 2095545
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Favism in a Portuguese family due to a deficient glucose-phosphate dehydrogenase variant (Canton) or (cpanton-like) type.
    Kahn A; Marie J; Desbois JC; Boivin P
    Acta Haematol; 1976; 56(1):58-64. PubMed ID: 822676
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Family investigations of erythrocyte glucose-6-phosphate dehydrogenase in favism.
    Rozynkowa D; Gebala A; Zagórski Z
    Pol Med J; 1970; 9(5):1093-9. PubMed ID: 5510280
    [No Abstract]   [Full Text] [Related]  

  • 14. Two commonly occurring nucleotide base substitutions in Chinese G6PD variants.
    Chiu DT; Zuo L; Chen E; Chao L; Louie E; Lubin B; Liu TZ; Du CS
    Biochem Biophys Res Commun; 1991 Oct; 180(2):988-93. PubMed ID: 1953767
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 74(1):71-3. PubMed ID: 2498187
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mediterranean glucose-6-phosphate dehydrogenase (G6PD(C563T)) mutation among Jordanian females with acute hemolytic crisis.
    Al-Alimi AA; Kanakiri N; Kamil M; Al-Rimawi HS; Zaki AH; Yusoff NM
    J Coll Physicians Surg Pak; 2010 Dec; 20(12):794-7. PubMed ID: 21205543
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.