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Hemoglobin|May 14, 2020
Distribution of Red Blood Cell Alloantibodies Among Transfusion-Dependent β-Thalassemia Patients in Different Population of Iran: Effect of EthnicityReyhaneh Sarihi, Naser Amirizadeh, Arezoo Oodi, et al.Hemoglobin|July 16, 2015
Five Years of Deferasirox Therapy for Cardiac Iron in β-Thalassemia MajorEfthymia Vlachaki, Alexandra Agapidou, Georgios Spanos, et al.Hemoglobin|July 22, 2015
The Prevalence and Spectrum of α-Thalassemia in Guizhou Province of South ChinaSheng-Wen Huang, Yin Xu, Xing-Mei Liu, et al.Hemoglobin|July 22, 2015
Homozygosity for the AATAAA > AATA- - Polyadenylation Site Mutation on the α2-Globin Gene Causing Transfusion-Dependent Hb H Disease in an Iranian Patient: A Case ReportSamaneh Farashi, Negin F Garous, Mehri Ashki, et al.Hemoglobin|January 1, 1985
High performance liquid chromatographic separation of the globin chains of non-human hemoglobinsW A Schroeder, J B Shelton, J R Shelton, et al.Hemoglobin|August 19, 2016
A novel 6.3 kb deletion and the Rare 27.6 kb Deletion Causing α+-Thalassemia in two Chinese PatientsXian-Yao Wang, Ming-Xiang Lin, Min LinHemoglobin|August 19, 2016
Phenotypic Diversity of Sickle Cell Disease in Patients with a Double Heterozygosity for Hb S and Hb D-PunjabLidiane S Torres, Jéssika V Okumura, Édis Belini-Júnior, et al.Hemoglobin|August 19, 2016
A Number of Cases in Iran Presenting with Coinheritance of Hemoglobin-H Disease and Beta-Thalassemia MinorTahereh Zarei, Javad Dehbozorgian, Jaber Imanifard, et al.Hemoglobin|June 20, 2020
COVID-19 in a Patient with β-Thalassemia Major and Severe Pulmonary Arterial HypertensionValeria M Pinto, Giorgio E Derchi, Lorenzo Bacigalupo, et al.Hemoglobin|June 20, 2020
Further Characterization of Hb Bronovo [α103(G10)His→Leu; HBA2: c.311A>T] and First Report of the Homozygous StateNikita Mehta, J Martin Johnston, Molly Hein, et al.Pageof 240