612 related articles for article (PubMed ID: 16513531)
1. 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]
2. 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]
3. Molecular basis of favism triggered by ingestion of frozen pumpkin cross-contaminated with fava beans.
Minucci A; Onori ME; Mazzuccato G; Urbani A; Capoluongo E
Clin Biochem; 2019 Jul; 69():45-47. PubMed ID: 31152693
[No Abstract] [Full Text] [Related]
4. 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]
5. Favism, the commonest form of severe hemolytic anemia in Palestinian children, varies in severity with three different variants of G6PD deficiency within the same community.
Reading NS; Sirdah MM; Shubair ME; Nelson BE; Al-Kahlout MS; Al-Tayeb JM; Aboud LN; Shaban MA; Luzzatto L; Prchal JT
Blood Cells Mol Dis; 2016 Sep; 60():58-64. PubMed ID: 27519946
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. [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]
9. Favism: looking for an autosomal gene associated with glucose-6-phosphate dehydrogenase deficiency.
Mareni C; Repetto L; Forteleoni G; Meloni T; Gaetani GF
J Med Genet; 1984 Aug; 21(4):278-80. PubMed ID: 6436490
[TBL] [Abstract][Full Text] [Related]
10. Three major glucose-6-phosphate dehydrogenase-deficient polymorphic variants identified in Mazandaran state of Iran.
Mesbah-Namin SA; Sanati MH; Mowjoodi A; Mason PJ; Vulliamy TJ; Noori-Daloii MR
Br J Haematol; 2002 Jun; 117(3):763-4. PubMed ID: 12028056
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Prevalence and molecular characterization of glucose-6-phosphate dehydrogenase deficiency in northern Thailand.
Charoenkwan P; Tantiprabha W; Sirichotiyakul S; Phusua A; Sanguansermsri T
Southeast Asian J Trop Med Public Health; 2014 Jan; 45(1):187-93. PubMed ID: 24964669
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Malays.
Ainoon O; Yu YH; Amir Muhriz AL; Boo NY; Cheong SK; Hamidah NH
Hum Mutat; 2003 Jan; 21(1):101. PubMed ID: 12497642
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Possible association of 3' UTR +357 A>G, IVS11-nt 93 T>C, c.1311 C>T polymorphism with G6PD deficiency.
Sirdah MM; Shubair ME; Al-Kahlout MS; Al-Tayeb JM; Prchal JT; Reading NS
Hematology; 2017 Jul; 22(6):370-374. PubMed ID: 28059001
[TBL] [Abstract][Full Text] [Related]
17. [Favism after ingestion of fava beans in a three-year-old child with glucose-6-phosphate dehydrogenase deficiency].
Sköld MB; Svendsen RP; Pedersen EB
Ugeskr Laeger; 2017 May; 179(20):. PubMed ID: 28504635
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [The genotype analysis of glucose-6-phosphate dehydrogenase deficiency in Yunnan province].
Yang Z; Chu J; Ban G; Huang X; Xu S; Li M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Aug; 18(4):259-63. PubMed ID: 11484161
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]