Last Updated: 09/26/2026
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Found 18 publications
Testing the Accuracy of Administrative Case Definitions to Identify Thalassemia.
Journal: Public health reports (Washington, D.C. : 1974)
Published: January 28, 2026
Newborn Screening for Sickle Cell Disease and Thalassemia.
Journal: JAMA health forum
Published: March 07, 2025
Transfusion management in thalassemia.
Journal: Annals of the New York Academy of Sciences
Published: August 02, 2023
Decision-making about gene therapy in transfusion dependent thalassemia.
Journal: BMC pediatrics
Published: May 07, 2022
Lessons Learned from OpenNotes Learning Mode and Subsequent Implementation across a Pediatric Health System.
Journal: Applied clinical informatics
Published: January 26, 2022
Influence of user-centered clinical decision support on pediatric blood product ordering errors.
Journal: Blood transfusion = Trasfusione del sangue
Published: November 25, 2021
A synonymous coding variant that alters ALAS2 splicing and causes X-linked sideroblastic anemia.
Journal: Pediatric blood & cancer
Published: August 05, 2021
An update on the US adult thalassaemia population: a report from the CDC thalassaemia treatment centres.
Journal: British journal of haematology
Published: June 17, 2021
SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature.
Journal: Human mutation
Published: January 26, 2021
Eculizumab for complement mediated thrombotic microangiopathy in sickle cell disease.
Journal: Haematologica
Published: July 30, 2020
Formative Usability Testing Reduces Severe Blood Product Ordering Errors.
Journal: Applied clinical informatics
Published: December 26, 2019
Mutations in the iron-sulfur cluster biogenesis protein HSCB cause congenital sideroblastic anemia.
Journal: The Journal of clinical investigation
Published: December 06, 2019
Last Updated: 09/26/2026