170 related articles for article (PubMed ID: 7959695)
1. A novel single-base mutation in the glucose 6-phosphate dehydrogenase gene is associated with chronic non-spherocytic haemolytic anaemia.
Filosa S; Cai W; Galanello R; Cao A; de Mattia D; Schettini F; Martini G
Hum Genet; 1994 Nov; 94(5):560-2. PubMed ID: 7959695
[TBL] [Abstract][Full Text] [Related]
2. Molecular basis of chronic non-spherocytic haemolytic anaemia: a new G6PD variant (393 Arg----His) with abnormal KmG6P and marked in vivo instability.
Filosa S; Calabrò V; Vallone D; Poggi V; Mason P; Pagnini D; Alfinito F; Rotoli B; Martini G; Luzzatto L
Br J Haematol; 1992 Jan; 80(1):111-6. PubMed ID: 1536798
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Molecular characterisation of an Italian G6PD variant responsible for chronic non-spherocytic haemolytic anaemia.
Martinez di Montemuros F; Cappellini MD; Dotti C; Tavazzi D; De Bellis G; Debernardi S; Fiorelli G
Clin Genet; 1994 Nov; 46(5):357-9. PubMed ID: 7889645
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. G6PD (Dublin): chronic non-spherocytic haemolytic anaemia resulting from glucose-6-phosphate dehydrogenase deficiency in an Irish kindred.
McCann SR; Smithwick AM; Temperley IJ; Tipton K
J Med Genet; 1980 Jun; 17(3):191-3. PubMed ID: 7401130
[TBL] [Abstract][Full Text] [Related]
7. Chronic non-spherocytic haemolytic disorders associated with glucose-6-phosphate dehydrogenase variants.
Fiorelli G; Martinez di Montemuros F; Cappellini MD
Baillieres Best Pract Res Clin Haematol; 2000 Mar; 13(1):39-55. PubMed ID: 10916677
[TBL] [Abstract][Full Text] [Related]
8. Chronic nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency: report of two families with novel mutations causing G6PD Bangkok and G6PD Bangkok Noi.
Tanphaichitr VS; Hirono A; Pung-amritt P; Treesucon A; Wanachiwanawin W
Ann Hematol; 2011 Jul; 90(7):769-75. PubMed ID: 21302115
[TBL] [Abstract][Full Text] [Related]
9. Two new mutations of the glucose-6-phosphate dehydrogenase (G6PD) gene associated with haemolytic anaemia: clinical, biochemical and molecular relationships.
Zarza R; Pujades A; Rovira A; Saavedra R; Fernandez J; Aymerich M; Vives Corrons JL
Br J Haematol; 1997 Sep; 98(3):578-82. PubMed ID: 9332310
[TBL] [Abstract][Full Text] [Related]
10. G6PD sumaré: a novel mutation in the G6PD gene (1292 T-->G) associated with chronic nonspherocytic anemia.
Saad ST; Salles TS; Arruda VR; Sonati MF; Costa FF
Hum Mutat; 1997; 10(3):245-7. PubMed ID: 9298828
[No Abstract] [Full Text] [Related]
11. Direct detection for G6PD Bangkok and G6PD Bangkok Noi mutations in the families with chronic nonspherocytic hemolytic anemia (CNSHA).
Glomglao W; Chansing K; Treesucon A; Siraprapapat P; Thongnoppakhun W; Sanpakit K; Tanphaichitr VS
Int J Lab Hematol; 2015 Apr; 37(2):e21-4. PubMed ID: 24923766
[No Abstract] [Full Text] [Related]
12. Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemia.
Vulliamy TJ; Kaeda JS; Ait-Chafa D; Mangerini R; Roper D; Barbot J; Mehta AB; Athanassiou-Metaxa M; Luzzatto L; Mason PJ
Br J Haematol; 1998 Jun; 101(4):670-5. PubMed ID: 9674740
[TBL] [Abstract][Full Text] [Related]
13. Glucose-6-phosphate dehydrogenase Durham: a de novo mutation associated with chronic hemolytic anemia.
Zimmerman SA; Ware RE; Forman L; Westwood B; Beutler E
J Pediatr; 1997 Aug; 131(2):284-7. PubMed ID: 9290617
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Molecular analysis of eight biochemically unique glucose-6-phosphate dehydrogenase variants found in Japan.
Hirono A; Fujii H; Takano T; Chiba Y; Azuno Y; Miwa S
Blood; 1997 Jun; 89(12):4624-7. PubMed ID: 9192788
[TBL] [Abstract][Full Text] [Related]
16. Three new exon 10 glucose-6-phosphate dehydrogenase mutations.
Beutler E; Westwood B; Melemed A; Dal Borgo P; Margolis D
Blood Cells Mol Dis; 1995; 21(1):64-72. PubMed ID: 7655862
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. 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]
19. G6Pd Kanazawa: a new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
Kitao T; Ito K; Hattori K; Matsuki T; Yoneyama Y
Acta Haematol; 1982; 68(2):131-5. PubMed ID: 6812368
[TBL] [Abstract][Full Text] [Related]
20. [The C1155G mutation of the red blood cell glucose-6-phosphate dehydrogenase gene in a subject with severe hereditary chronic nonspherocytic anaemia].
Burzyńska B; Adamowicz-Salach A; Płochocka D; Gołaszewska E; Witos I
Med Wieku Rozwoj; 2009; 13(2):136-9. PubMed ID: 19837994
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
