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Hemoglobin|November 20, 2018
Frequency of α-Globin Gene Triplications and Coinheritance with β-Globin Gene Mutations in the Iranian PopulationSeyedeh Sedigheh Abedini, Fatemeh Forouzesh Pour, Keyvan Karimi, et al.Hemoglobin|April 8, 2017
A Comprehensive Molecular Investigation of α-Thalassemia in an Iranian Cohort from Different Provinces of North IranHajar Eftekhari, Ahmad Tamaddoni, Hassan Mahmoudi Nesheli, et al.Hemoglobin|July 13, 2019
Quadrupole-Time-of-Flight Mass Spectrometric Identification of Hemoglobin Subunits α, β, γ and δ in Unknown Peaks of High Performance Liquid Chromatography of Hemoglobin in β-ThalassemiasUday Y H Abdullah, Hishamshah M Ibrahim, Noraesah B Mahmud, et al.Hemoglobin|July 16, 2019
First Description of Hb San Diego (HBB: c.328G>A) in a Chinese Family with Congenital ErythrocytosisHuixia Xiong, Suning ChenHemoglobin|February 16, 2008
Effects of combined deferiprone and deferoxamine chelation therapy on iron load indices in beta-thalassemiaMaria Tsironi, George Assimakopoulos, Katerina Polonofi, et al.Hemoglobin|February 16, 2008
Effects of chelation therapy on cardiac function improvement in thalassemia patients: literature review and the Taiwanese experienceChing-Tien Peng, Chang-Hai Tsai, Kang-Hsi WuHemoglobin|February 16, 2008
Can iron chelators influence the progression of atherosclerosis?Joannes J M Marx, Apriliana E R Kartikasari, Niki A GeorgiouHemoglobin|February 16, 2008
A new approach for potential combined chelation therapy using mono- and bis-hydroxypyridinonesM Amélia Santos, Sofia Gama, Marco Gil, et al.Hemoglobin|February 16, 2008
Chelators controlling metal metabolism and toxicity pathways: applications in cancer prevention, diagnosis and treatmentGeorge J Kontoghiorghes, Aglaia Efstathiou, Stella Ioannou-Loucaides, et al.Hemoglobin|November 9, 2021
A Case of Fat Embolism Syndrome with Cerebral Involvement in Sickle Cell AnemiaRochelle G Melvin, Zachary Liederman, Sumedha Arya, et al.Pageof 240