Results 141 to 150 of about 78,171 (294)

Electronic heath record phenotypes to classify sickle cell anemia versus other subtypes of sickle cell disease in the ASH RC data hub [PDF]

Charity I Oyedeji, Nathan A. Bihlmeyer, Mariam Kayle, Jennifer Rothman, Rachel A. Myers, John J. Strouse   +5 more
openalex   +1 more source

Enhanced fetal hemoglobin production by phenylacetate and 4- phenylbutyrate in erythroid precursors derived from normal donors and patients with sickle cell anemia and beta-thalassemia [PDF]

, 1993
Eitan Fibach, P Prasanna, GP Rodgers, Dvorit Samid   +3 more
openalex   +1 more source

Cell and Gene Therapy in Equine Ocular Disease

Veterinary Ophthalmology, Volume 29, Issue 2, March 2026.
ABSTRACT Equine ocular disease is common and often challenging to treat using traditional methods. This has led to the development of new therapies. Like human medicine, veterinary medicine is adopting cellular and gene therapy as innovative approaches. Equine ocular disease is a particularly promising area for these techniques.
Kimberly A. S. Young, Lauren V. Schnabel, Brian C. Gilger   +2 more
wiley   +1 more source

Campus Update: January/February 1993 v. 5, no. 1 [PDF]

, 1993
Monthly newsletter of the BU Medical ...
Boston University Medical Center
core   +1 more source

Low Rate of RBC Alloimmunization Among Transfused Children with Sickle Cell Anemia in Malawi Without Pre-Transfusion Screening or Antigen Matching [PDF]

April Evans, Kristina Prus, Apatsa Matatiyo, Gugulethu Mapurisa, Memory Nonganonga, Manley Kamija, Kambe Banda-Zgambo, Timothy Mutafya, Meffa Misiri, Rizine Mzikamanda, Katherine D. Westmoreland, Russell E. Ware   +11 more
openalex   +1 more source

THE ROLE OF HU IN THE MANAGEMENT OF VASO-OCCLUSIVE CRISES IN SICKLE CELL ANEMIA. [PDF]

, 2017
Dr.MattarAl Sulami, Dr.SalwaAl Najjar., Dr.SalwaAl Najjar.   +2 more
openalex   +1 more source

Incidence of adverse events in iron‐deficient pregnant women and surgical patients undergoing intravenous iron treatment with ferric isomaltose or ferric carboxymaltose: A systematic review

Transfusion, EarlyView.
Dominik Heger, Johannes Volkmann, Stephanie Weibel, Johanna Stoevesandt, Veronika Walzer, Peter Kranke, Patrick Meybohm, Stephanie Stangl   +7 more
wiley   +1 more source

Relation of Adverse Childhood Experiences to Clinical and Patient‐Reported Outcomes for Adults With Sickle Cell Disease: A Registry Study

Pediatric Blood &Cancer, Volume 73, Issue 2, February 2026.
ABSTRACT Background Adverse childhood experiences (ACEs) are stressful or traumatic events prior to age 18 that are known to have a lasting impact on individuals’ health and well‐being. There is a gap in understanding the relationship between ACEs and Other Life Stressors and health status for adults with sickle cell disease (SCD).
Marsha Treadwell, Jessica Liang, Liliana Preiss, Angela Rivers, Jane S. Hankins, Allison King, Justin Williams, Michael B. Potter, Danielle Hessler   +8 more
wiley   +1 more source

Age dependence of the gene frequency of alpha-thalassemia in sickle cell anemia in Cuba [letter] [PDF]

, 1996
Gustavo Aroca, Ana Veruska Cruz da Silva, Eva Svarch, Enrique Espinosa, RL Nagel   +4 more
openalex   +1 more source

Economic Burden of Sickle Cell Disease: A Retrospective Study of Pediatric and Adult Individuals With Medicaid Coverage From 2016 to 2020

American Journal of Hematology, Volume 101, Issue 2, Page 269-280, February 2026.
ABSTRACT There is limited information regarding the contemporary real‐world clinical and financial burden of Medicaid enrollees with sickle cell disease (SCD) in the United States. Using the IBM MarketScan Medicaid database (7/2016–12/2020), individuals with ≥ 3 SCD diagnoses were matched 1:1 on age, gender, and race to individuals without SCD ...
Giovanna Tedesco Barcelos, Telma Peixoto, Jose Alvir, Jay Lin, Christine L. Baker   +4 more
wiley   +1 more source