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Hemoglobin|November 30, 2018
Effect of Assorted Globin Haplotypes and α-Thalassemia on the Clinical Heterogeneity of Hb S-β-ThalassemiaPreetinanda M Dash, Praveen K Sahu, Siris Patel, et al.Hemoglobin|February 28, 2018
Complex Interaction of Hb Q-Thailand (HBA1: c.223G>C) with β-Thalassemia/Hb E (HBB: c.79G>A) DiseaseSitthichai Panyasai, Surada Satthakarn, Sakorn PornprasertHemoglobin|March 18, 2021
Relation of Serum Ferritin Level with Serum Hepcidin and Fucose Levels in Children with β-Thalassemia MajorSalah H Al-Zuhairy, Mohammed A Darweesh, Mohammed A-M OthmanHemoglobin|December 27, 2021
Dominant β-Thalassemia Phenotype Caused by Hb Dieppe (HBB: c.383A>G): Another Case ReportHuan-Qing Chen, Li-Sha Wu, Fan Jiang, et al.Hemoglobin|February 16, 2021
Venous Thromboembolism in Sickle Cell Disease is Associated with NeutrophiliaJahnavi Gollamudi, Shashank Sarvepalli, Animesh Vadaparti Binf, et al.Hemoglobin|February 9, 2021
Chronic Hemolysis May Adversely Affect Skeletal Health. A Cross-Sectional Study of a Pediatric PopulationArtemis Doulgeraki, Christine Fragodimitri, Helen Athanasopoulou, et al.Hemoglobin|February 24, 2021
Hb S (HBB: c.20A>T) Characteristics by High Performance Liquid Chromatography in Patients with Sickle Cell Disease Receiving the Novel Agent VoxelotorDimitris A Tsitsikas, Mawlid Kamal, Adeyinka Braimoh, et al.Hemoglobin|April 1, 2017
Lactate Dehydrogenase: A Marker of the Severity of Vaso-Occlusive Crisis in Children with Sickle Cell Disease Presenting at the Emergency DepartmentMarina García-Morin, Carolina López-Sangüos, Paula Vázquez, et al.Hemoglobin|April 1, 2017
First Report of a Chinese Family Carrying a Double Heterozygosity for Hb Q-Thailand and Hb J-BangkokFan Jiang, Jian-Ying Zhou, Jin-Mei Yan, et al.Hemoglobin|April 1, 2017
A Case of Fatal Agranulocytosis That Developed in a Patient with β-Thalassemia Major Treated with DeferiproneMaria Mainou, Aggeliki Kotsiafti, Philippos Klonizakis, et al.Pageof 239