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Hemoglobin|May 22, 2020
Hb Westmead (HBA2: c.369C>G): Hematological Characteristics in Heterozygotes with and without α0-ThalassemiaFan Jiang, Ai-Ping Ju, Jian Li, et al.Hemoglobin|August 5, 2022
Adherence to Iron Chelation Therapy among Adults with Thalassemia: A Systematic ReviewMargaret Locke, Paavani S Reddy, Sherif M BadawyHemoglobin|August 5, 2022
Hepcidin-to-Ferritin Ratio as an Early Diagnostic Index of Iron Overload in β-Thalassemia Major PatientsBurhan A Zaman, Shereen A IbrahimHemoglobin|January 1, 1978
Hemoglobin Hoshida (beta43 (cd-2) Glu leads to Gln), a new hemoglobin variant discovered in JapanI Iuchi, S Ueda, K Hidaka, et al.Hemoglobin|January 1, 1978
Hemoglobin Legnano (alpha2 141 (HC3) Arg replaced by Leu beta2): a new abnormal human hemoglobin with high oxygen affinityF Mavilio, M Marinucci, L Tentori, et al.Hemoglobin|January 1, 1989
Hb Fontainebleau [alpha 21(B2)Ala----pro], a new silent mutant hemoglobinH Wajcman, Y Blouquit, G Gombaud-Saintonge, et al.Hemoglobin|June 2, 2015
Heart Rate Variability for Early Detection of Iron Overload Cardiomyopathy in β-Thalassemia PatientsNut Koonrungsesomboon, Adisak Tantiworawit, Arintaya Phrommintikul, et al.Hemoglobin|April 22, 2015
Hb H Hydrops Fetalis Syndrome Caused by Association of the - -(SEA) Deletion and Hb Constant Spring (HBA2: c.427T > C) Mutation in a Chinese FamilySheng He, Chenguang Zheng, Dahua Meng, et al.Hemoglobin|May 7, 2020
Hb S (HBB: c.20A>T) and α- and β-Thalassemia Coinheritance in Iranian PatientsAzita Azarkeivan, Nader Cohan, Hamid Reza Niazkar, et al.Hemoglobin|May 2, 2020
Concomitant Existence of Paroxysmal Nocturnal Hemoglobinuria in a Patient with Hb E (HBB: c.79G>A) TraitRohan Halder, Uday Kumar D Sundaram, Karthika K Veetil, et al.Pageof 240