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Hemoglobin|August 11, 2022
Thalassemia in ThailandKittiphong Paiboonsukwong, Yupin Jopang, Pranee Winichagoon, et al.Hemoglobin|August 18, 2022
β-Thalassemia Intermedia Caused by the β-Globin Gene 3' Untranslated Region: Another Case ReportFan Jiang, Gui-Lan Chen, Jian Li, et al.Hemoglobin|August 12, 2022
Hb Kirikiriroa [α57(E6)Gly→Cys; HBA1: c.172G>T]: A Novel Unstable α-Globin Variant with Oxidized Derivatives Interfering with Hb A1cJordyn A Moore, Beverley M Pullon, Darrell Wang, et al.Hemoglobin|August 4, 2022
Levels of Serum Ferritin and Hepcidin in Patients with Uncomplicated Falciparum Malaria in Hodeidah, Yemen: Considerations for Assessing Iron StatusAmal A Al-Azazi, Rashad Abdul-Ghani, Mona H El-Sayad, et al.Hemoglobin|August 5, 2022
A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 LevelsTaner Karakaya, Fatma Silan, Ozturk OzdemirHemoglobin|February 23, 2023
Severe Hb H Disease Caused by Hb Zürich-Albisrieden (HBA1: c.178G>C): Another Case ReportShao-Min Wu, Su-Ran Huang, Chan Li, et al.Hemoglobin|March 3, 2023
Novel Promoter Mutation (HBB:C.-139_-138del) Associated with β-Thalassemia Trait Detected by Next-Generation Sequencing in Southern ChinaLei Pan, Peirun Tian, Shiping Chen, et al.Hemoglobin|June 6, 2020
Severe α-Thalassemia Due to Compound Heterozygosity for Hb Adana (α59 Gly>Asp) (HBA1: c.179G > A) and Codon 127 (A > T) (HBA2: c.382A > T) in an Iranian FamilyAzam Azimi, Susan Tahmasebi, Keivan Moradi, et al.Hemoglobin|May 26, 2020
Proficiency Testing Program for Hb E (HBB: c.79G>A) Screening in Thailand Using Lyophilized Hb E Control MaterialsSakorn Pornprasert, Sirithorn Surajinda, Panida Pongpunyayuen, et al.Pageof 238