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Hemoglobin|December 23, 2011
Secondary mutation (c.94_95delAG) in a -α3.7 allele associated with Hb H disease in two unrelated African American individuals homozygous for the -α(3.7) deletion (-α3.7/-α3.7T)Po Zhao, Arlene M Buller-Burckle, Mei Peng, et al.Hemoglobin|December 23, 2011
Towards a prevention program for β-thalassemia. The molecular spectrum in East Java, IndonesiaPratika Yuhyi Hernanda, Luluk Tursilowati, Sandra G J Arkesteijn, et al.Hemoglobin|July 30, 2011
Molecular analysis of β-thalassemia patients: first identification of mutations HBB:c.93-2A>G and HBB:c.114G>A in BrazilAndrea Cristina Fernandes, Marily Maria Azevedo Shimmoto, Gilberto Koiti Furuzawa, et al.Hemoglobin|July 30, 2011
Sickle cell/β0-thalassemia associated with the 1393 bp deletion can be associated with a severe phenotypeYvonne Daniel, Kim Hill, Baba Inusa, et al.Hemoglobin|May 24, 2011
Sequential alternating deferiprone and deferoxamine treatment compared to deferiprone monotherapy: main findings and clinical follow-up of a large multicenter randomized clinical trial in -thalassemia major patientsGaetano Restivo Pantalone, Aurelio Maggio, Angela Vitrano, et al.Hemoglobin|May 24, 2011
A quantitative evaluation of redox-active compounds in human blood lipidsAlexander V Lebedev, Vaclav Pelouch, Marina V Ivanova, et al.Hemoglobin|May 24, 2011
Stability and reactivity of free radicals: a physicochemical perspective with biological implicationsTatiana Yu Karogodina, Svetlana V Sergeeva, Dmitri V StassHemoglobin|January 1, 1990
Spin label probes of the environment of cysteine beta-93 in hemoglobinP T Manoharan, J T Wang, K Alston, et al.Hemoglobin|November 30, 2011
Effect of co-inheritance of β-thalassemia and hemochromatosis mutations on iron overloadHerminio López-Escribano, Joana F Ferragut, Maria M Parera, et al.Pageof 240