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248 related items for PubMed ID: 21205543
1. 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 [Abstract] [Full Text] [Related]
9. [Favism in Polish families]. Jabłońska-Skwiecińska E, Pogłód R, Skrobowska A. Pol Tyg Lek; 2010 Dec; 45(38-39):778-81. PubMed ID: 2095545 [Abstract] [Full Text] [Related]
10. Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Kurdish population of Western Iran. Rahimi Z, Vaisi-Raygani A, Nagel RL, Muniz A. Blood Cells Mol Dis; 2006 Dec; 37(2):91-4. PubMed ID: 16938474 [Abstract] [Full Text] [Related]
17. Unsuspected glucose-6-phosphate dehydrogenase deficiency presenting as symptomatic methemoglobinemia with severe hemolysis after fava bean ingestion in a 6-year-old boy. Odièvre MH, Danékova N, Mesples B, Chemouny M, Couque N, Parez N, Ducrocq R, Elion J. Int J Hematol; 2011 May; 93(5):664-666. PubMed ID: 21479984 [Abstract] [Full Text] [Related]
18. 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 May; 60(3):216-21. PubMed ID: 7106752 [Abstract] [Full Text] [Related]