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Hemoglobin|August 19, 2016
Patient Involvement as Experts in the Development and Assessment of a Smartphone App as a Patient Education Tool for the Management of Thalassemia and Iron Overload SyndromesRichard Ward, Karim M Taha
Hemoglobin|April 21, 2020
Effect of the Hydoxyurea in Yemeni Transfusion-Dependent β-Thalassemia PatientsHafiz A Al-Nood, Rasha M Al-Nood, Najeeb S Ghanem, et al.
Hemoglobin|August 7, 2025
Therapeutic Response to Hydroxyurea in Beta-Thalassemia Intermedia with Rare Mutation: A Case ReportHassan Fawaz, Mohammad Hassan Hodroj, Nicole Charbel, et al.
Hemoglobin|August 13, 2025
HbH Disease in an Elderly Man Due to Compound Heterozygosity for Deletional α-Thalassemia and Hb Dubai (HBA2:c.368A > T)T Ruchika Devi, Prasad Dange, Roopam Deka, et al.
Hemoglobin|January 1, 1983
Characterization and properties of Hb York (beta 146 His leads to Pro)H Kosugi, A S Weinstein, K Kikugawa, et al.
Hemoglobin|May 13, 2021
Clinical Features and Outcome of Sickle Cell Disease in a Tertiary Center in Northern Lebanon: A Retrospective Cohort Study in a Local, Hospital-Associated RegistryAdlette Inati, Chadi Al Alam, Cristel El Ojaimi, et al.
Hemoglobin|May 26, 2021
Detection of the HBB: c.393T>G Mutation in Two Patients with Hypochromic Microcytic AnemiaQiang Zhao, Su-Min Zhao, Xue Zhang, et al.
Hemoglobin|July 2, 2025
A Rare Hemoglobin Variant Detected for the First Time in Türkiye (Hb Iraq-Halabja): Evaluation of the Effect of Variant Hemoglobins on HbA1c MethodsTevfik Balcı, Beyza Ünlü, Müşerref Başdemirci, et al.
Hemoglobin|July 27, 2025
Coexistence of Mycoplasma Pneumonia and Pulmonary Embolism as a Cause of Acute Chest Syndrome in a Child with Sickle Cell DiseaseLucía Rodríguez-Noriega Béjar, Clara Simón Bernaldo de Quirós, Soledad González Muñíz, et al.
Hemoglobin|December 11, 2025
Identification of a Patient with Transfusion-Dependent β-Thalassemia Caused by Compound Heterozygous Mutations of HBB: C.84_85insC and Common Linked Intronic Variants in HBBLang Qin, Xinyu Li, Yin Wang, et al.
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