218 related articles for article (PubMed ID: 8956035)
1. Independent origin of single and double mutations in the human glucose 6-phosphate dehydrogenase gene.
Vulliamy T; Rovira A; Yusoff N; Colomer D; Luzzatto L; Vives-Corrons JL
Hum Mutat; 1996; 8(4):311-8. PubMed ID: 8956035
[TBL] [Abstract][Full Text] [Related]
2. [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]
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. 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]
5. Both mutations in G6PD A- are necessary to produce the G6PD deficient phenotype.
Town M; Bautista JM; Mason PJ; Luzzatto L
Hum Mol Genet; 1992 Jun; 1(3):171-4. PubMed ID: 1303173
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
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. Definition of the mutations of G6PD Wayne, G6PD Viangchan, G6PD Jammu, and G6PD 'LeJeune'.
Beutler E; Westwood B; Kuhl W
Acta Haematol; 1991; 86(4):179-82. PubMed ID: 1805484
[TBL] [Abstract][Full Text] [Related]
10. Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East.
Kurdi-Haidar B; Mason PJ; Berrebi A; Ankra-Badu G; al-Ali A; Oppenheim A; Luzzatto L
Am J Hum Genet; 1990 Dec; 47(6):1013-9. PubMed ID: 1978555
[TBL] [Abstract][Full Text] [Related]
11. Molecular heterogeneity of the glucose-6-phosphate dehydrogenase deficiency in the Hellenic population.
Menounos P; Zervas C; Garinis G; Doukas C; Kolokithopoulos D; Tegos C; Patrinos GP
Hum Hered; 2000; 50(4):237-41. PubMed ID: 10782016
[TBL] [Abstract][Full Text] [Related]
12. Molecular abnormality of G6PD Konan and G6PD Ube, the most common glucose-6-phosphate dehydrogenase variants in Japan.
Hirono A; Fujii H; Miwa S
Hum Genet; 1993 Jun; 91(5):507-8. PubMed ID: 8100211
[TBL] [Abstract][Full Text] [Related]
13. Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Eastern Province of Saudi Arabia.
Al-Ali AK; Al-Mustafa ZH; Al-Madan M; Qaw F; Al-Ateeq S
Clin Chem Lab Med; 2002 Aug; 40(8):814-6. PubMed ID: 12392311
[TBL] [Abstract][Full Text] [Related]
14. Two new class III G6PD variants [G6PD Tunis (c.920A>C: p.307Gln>Pro) and G6PD Nefza (c.968T>C: p.323 Leu>Pro)] and overview of the spectrum of mutations in Tunisia.
Benmansour I; Moradkhani K; Moumni I; Wajcman H; Hafsia R; Ghanem A; Abbès S; Préhu C
Blood Cells Mol Dis; 2013 Feb; 50(2):110-4. PubMed ID: 22963789
[TBL] [Abstract][Full Text] [Related]
15. Three new mutations account for the prevalence of glucose 6 phosphate deshydrogenase (G6PD) deficiency in Tunisia.
Bendaoud B; Hosni I; Mosbahi I; Hafsia R; Prehu C; Abbes S
Pathol Biol (Paris); 2013 Apr; 61(2):64-9. PubMed ID: 22552160
[TBL] [Abstract][Full Text] [Related]
16. Detection of point mutations in exon 2 of the G6PD gene in Chinese G6PD variants.
Xu W; Wang J; Hua X; Du C
Chin Med Sci J; 1994 Mar; 9(1):20-3. PubMed ID: 8086629
[TBL] [Abstract][Full Text] [Related]
17. Heterogeneity of "Mediterranean type" glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain and description of two new variants associated with favism.
Vives Corrons JL; Pujades A
Hum Genet; 1982; 60(3):216-21. PubMed ID: 7106752
[TBL] [Abstract][Full Text] [Related]
18. Molecular heterogeneity of G6PD deficiency in an Amazonian population and description of four new variants.
Hamel AR; Cabral IR; Sales TS; Costa FF; Olalla Saad ST
Blood Cells Mol Dis; 2002; 28(3):399-406. PubMed ID: 12367584
[TBL] [Abstract][Full Text] [Related]
19. Molecular characterization of G6PD deficiency in Southern Italy: heterogeneity, correlation genotype-phenotype and description of a new variant (G6PD Neapolis).
Alfinito F; Cimmino A; Ferraro F; Cubellis MV; Vitagliano L; Francese M; Zagari A; Rotoli B; Filosa S; Martini G
Br J Haematol; 1997 Jul; 98(1):41-6. PubMed ID: 9233561
[TBL] [Abstract][Full Text] [Related]
20. Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in the south of Thailand and identification of a novel variant (G6PD Songklanagarind).
Laosombat V; Sattayasevana B; Janejindamai W; Viprakasit V; Shirakawa T; Nishiyama K; Matsuo M
Blood Cells Mol Dis; 2005; 34(2):191-6. PubMed ID: 15727905
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
