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Hemoglobin|April 12, 2017
A Novel Mutation of the α2-Globin Gene Causing α+-Thalassemia: Hb Nanning (HBA2: c.369_370delinsGA)Biyan Chen, Li Lin, Shang Yi, et al.
Hemoglobin|November 11, 2021
Comparative Efficacy and Safety Between Deferiprone and Deferasirox with Special Reference to Serum Ferritin Level and Cardiac Function in Bengali β-Thalassemia Major ChildrenIsita Tripathy, Amrita Panja, Tuphan Kanti Dolai, et al.
Hemoglobin|August 20, 2019
Evaluation of the Effect of Support-Training System of Peer Group on Promotion of Self-Care in β-Thalassemia Major Patients in Southern IranSanaz Safaei, Heidarali Abedi, Shirin Parand, et al.
Hemoglobin|September 15, 2022
Hb Alessandria [β37(C3)Trp→Leu; HBB: c.113G>T]: a Novel Variant on the β-Globin Chain with Slightly Increased Affinity for Oxygen Detected by Capillary ElectrophoresisLara Calcagno, Maria M Ciriello, Monica Maccarini, et al.
Hemoglobin|February 19, 2021
Evaluation of the High Resolution Melting Approach for Detection of β-Thalassemia Gene MutationsAmna Tariq, Sana Khurshid, Muhammad Sajjad
Hemoglobin|September 13, 2022
Hemoglobinopathies and COVID-19: The Experience of a Center in Northern GreeceChristos Varelas, Eleni Gavriilaki, Ioanna Sakellari, et al.
Hemoglobin|November 1, 2022
Investigation of the Distribution of Thalassemia in Children in Jiangxi Province, the People's Republic of ChinaKe Wang, Ting Yi, Wen-Tao Wu, et al.
Hemoglobin|August 6, 2016
Electromobility Shift Assay Reveals Evidence in Favor of Allele-Specific Binding of RUNX1 to the 5' Hypersensitive Site 4-Locus Control RegionHossein Dehghani, Sepideh Ghobakhloo, Maryam Neishabury
Hemoglobin|August 6, 2016
Occurrence of the - -(SEA), - -(THAI) and - -(FIL) α-Thalassemia-1 Carriers from a 7-Year Study at Ramathibodi Hospital, Bangkok, ThailandKobkorn Pongjantharasatien, Wansa Banyatsuppasin, Sonnarong Pounsawat, et al.
Hemoglobin|August 6, 2016
Is Vitamin C Supplementation in Patients with β-Thalassemia Major Beneficial or Detrimental?Hadi Darvishi Khezri, Amir Emami Zeydi, Hassan Sharifi, et al.
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