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Hemoglobin|February 21, 2025
Hypersplenism Affects Growth and Haematology in HbSS: Observations from the Jamaican Birth CohortIan Hambleton, Karlene Mason, Beryl Serjeant, et al.
Hemoglobin|December 17, 2020
Exploration of Barriers and Facilitators to Optimal Emergency Department Care of Sickle Cell Disease: Opportunities for Patient-Physician Partnerships to Improve CareZachary Liederman, Naa Kwarley Quartey, Richard Ward, et al.
Hemoglobin|October 29, 2019
Association of the CCR5Δ32 Mutant Genotype with Sickle Cell Disease in Egyptian PatientsMaha H El Sissy, Ahmed A Hafez, Sherif E A Moneim, et al.
Hemoglobin|October 14, 2020
Hematopoietic Stem Cell Transplantation in Patients with HemoglobinopathiesM Akif Yesilipek
Hemoglobin|July 27, 2021
Hb Calgary (HBB: c.194G>T): A Highly Unstable Hemoglobin Variant with a β-Thalassemia Major PhenotypeGeorgina Martin, Runa M Grimholt, Doan Le, et al.
Hemoglobin|June 14, 2021
Correlation Between Serum Ferritin and Viral Hepatitis in Thalassemia PatientsNatthapat Rujeerapaiboon, Adisak Tantiworawit, Pokpong Piriyakhuntorn, et al.
Hemoglobin|January 1, 1986
Hemoglobinopathies in XinjiangH J Li, D X Liu, L Li, et al.
Hemoglobin|May 27, 2021
First Report of Nondeletional Hb H Disease Caused by an α2-Globin Gene Mutation: HBA2: c.184A>TQi Tian, Ya-Li Lei, Li-Li Xu, et al.
Hemoglobin|January 1, 1985
Hemoglobin kenitra alpha 2 beta 2 69 (E13) Gly----Arg. A new beta variant of elevated expression associated with alpha-thalassemia, found in a Moroccan womanJ Delanoe-Garin, N Arous, Y Blouquit, et al.
Hemoglobin|January 1, 1985
A new unstable, high oxygen affinity hemoglobin: Hb Nagoya or beta 97 (FG4) His----ProY Ohba, M Imanaka, M Matsuoka, et al.
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