Last Updated: 09/26/2026
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Found 57 publications
Transient neonatal hemolytic anemia due to the novel gamma globin gene mutation HBG2:C.290T>C, p.Leu97Pro (hemoglobin Wareham).
Journal: Pediatric blood & cancer
Published: July 12, 2022
Clinical phenotypes of three children with sickle cell disease caused by HbS/Sicilian (δβ)0 -thalassemia deletion.
Journal: American journal of hematology
Published: October 25, 2021
Pharmacologic induction of PGC-1α stimulates fetal haemoglobin gene expression.
Journal: British journal of haematology
Published: September 29, 2021
Strategies to improve pharmacogenomic-guided treatment options for patients with β-hemoglobinopathies.
Journal: Expert review of hematology
Published: September 07, 2021
A Novel β0-Thalassemia Mutation, HBB: c.356_357delTT [Codon 118 (-TT)] in an Iraqi Kurd.
Journal: Hemoglobin
Published: June 25, 2021
Alpha-thalassemia. Case report alpha-thalassemia in a Costa Rican family, A case report.
Journal: Clinical case reports
Published: September 26, 2020
When Hemoglobin Reported to Be A, S, and F Are Neither A, S, Nor F: A Tale of Two Patients.
Journal: The journal of applied laboratory medicine
Published: January 16, 2020
Interference of Hemoglobin A1c Due to Hemoglobin Franklin Park.
Journal: The journal of applied laboratory medicine
Published: October 23, 2019
An Unusual Case of Low Hemoglobin Oxygen Saturation.
Journal: Annals of the American Thoracic Society
Published: June 01, 2019
Inhibition of LSD1 by small molecule inhibitors stimulates fetal hemoglobin synthesis.
Journal: Blood
Published: April 18, 2019
BCL2L1 is associated with γ-globin gene expression.
Journal: Blood advances
Published: January 24, 2019
Last Updated: 09/26/2026