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Hemoglobin|January 1, 1985
Some properties of hemoglobin mobile (alpha 2 beta 2 73 Asp----Val)J L Converse, V Sharma, G Reiss-Rosenberg, et al.Hemoglobin|September 22, 2006
Accurate measurements of fetal hemoglobin for neonates with different gestational agesShyang-Yun Pamela K Shiao, Ching-Nan OuHemoglobin|September 22, 2006
Delta-thalassemia in CyprusEleni Pavlou, Marios Phylactides, Andriani Kyrri, et al.Hemoglobin|September 22, 2006
A newly identified deletion of 970 bp at the alpha-globin locus that removes the promoter region of the alpha1 geneJeroen Poodt, Henk A M Martens, Ita B B Walsh, et al.Hemoglobin|September 22, 2006
Molecular characterization of beta-thalassemia in the Dohuk region of IraqNasir A S Al-Allawi, Jalaldet M S Jubrael, Michael HughsonHemoglobin|July 26, 2008
Unstable and thalassemic alpha chain hemoglobin variants: a cause of Hb H disease and thalassemia intermediaHenri Wajcman, Jan Traeger-Synodinos, Ioannis Papassotiriou, et al.Hemoglobin|June 27, 2006
Haplotypes linked to three rare beta-thalassemia mutations, originally reported in TunisiaAmina Bibi, Taieb Messaoud, Slaheddine FattoumHemoglobin|June 27, 2006
Effective combination therapy of deferiprone and deferoxamine for the rapid clearance of excess cardiac IRON and the prevention of heart disease in thalassemia. The Protocol of the International Committee on Oral ChelatorsAnnita Kolnagou, George J KontoghiorghesHemoglobin|June 27, 2006
Comparison of oral and subcutaneous iron chelation therapies in the prevention of major endocrinopathies in beta-thalassemia major patientsChung-Hsing Wang, Kang-Hsi Wu, Fuu-Jen Tsai, et al.Hemoglobin|June 27, 2006
Pilot study on the "quality of life" as reflected by psychosocial adjustment of children with thalassemia major undergoing iron-chelating treatment in western TaiwanHuang-Tsung Kuo, Ming-Yu Tsai, Ching-Tien Peng, et al.Pageof 238