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Hemoglobin|June 1, 2005
Hb Geldrop St. Anna [beta94(FG1)Asp --> Tyr]: a new hemoglobin variant observed in a diabetic patientCornelis L Harteveld, Marc H M Thelen, Johannes J A Rutten, et al.Hemoglobin|June 1, 2005
Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of PalestineHisham M Darwish, Fadia F El-Khatib, Suhail AyeshHemoglobin|September 22, 2006
Observation of a rare hemoglobin variant [Hb Lulu island, beta107(G9)Gly-->Asp, GGC-->GAC] co-inherited with a beta+-thalassemia mutation [IVS-I-110 (G-->A)] or in the heterozygous state in a Greek-Albanian familyIoannis Papassotiriou, Alexandra Stamoulakatou, Henri Wajcman, et al.Hemoglobin|June 27, 2006
Liver fibrosis and iron levels during long-term deferiprone treatment of thalassemia major patientsShu-Fen Wu, Ching-Tien Peng, Kang-Hsi Wu, et al.Hemoglobin|June 27, 2006
A randomized controlled study evaluating the safety and efficacy of deferiprone treatment in thalassemia major patients from Hong KongShau-Yin Ha, Ki-Wai Chik, Siu-Cheung Ling, et al.Hemoglobin|June 27, 2006
Thalassemia treatment and prevention in Uva Province, Sri Lanka: a public opinion surveyRasnayaka M MudiyanseHemoglobin|May 9, 2007
Molecular basis of thalassemia in QatarAisha Al-Obaidli, Mowafak Hamodat, Zainab Fawzi, et al.Hemoglobin|May 9, 2007
Two new alpha-thalassemia frameshift mutationsHong-Yuang Luo, Adeboye H Adewoye, Monika Pilichowska, et al.Hemoglobin|May 9, 2007
A moderately severe alpha-thalassemia condition resulting from a combination of the alpha2 polyadenylation signal (AATAAA-->AATA- -) mutation and a 3.7 Kb alpha gene deletion in an Australian familyJohn F Prior, Erna Lim, Neela Lingam, et al.Hemoglobin|May 9, 2007
Sickle cell disease: a multigenic perspective of a single gene disorderAbdullah KutlarPageof 239