Identification of four common α-thalassemia gene deletions among a group with hemoglobinopathies in Sétif population, Algeria [PDF]
Bakhouche Houcher +4 more
openalex +1 more source
Reality bites: allocating gene therapy for hemoglobinopathies. [PDF]
Tubman VN, Fasipe TA.
europepmc +1 more source
Haploidentical HSCT for hemoglobinopathies: improved outcomes with TCRαβ+/CD19+-depleted grafts.
J. Gaziev +11 more
semanticscholar +1 more source
Alpha-Thalassemia Unmasked in a Patient With Sickle Cell Trait: A Case Report. [PDF]
Chuquimarca B +3 more
europepmc +1 more source
Systematic follow-up and case management of the abnormal newborn screen can improve acceptance of genetic counseling for sickle cell or other hemoglobinopathy trait [PDF]
Beth Kladny +2 more
openalex +1 more source
Development of a low-cost and high-throughput LC-MS method for newborn screening of thalassemia and abnormal hemoglobin disorders. [PDF]
Huang WX +7 more
europepmc +1 more source
Unexpectedly Low HbA1c in a Patient With Newly Diagnosed Diabetes Mellitus and Thalassemia Trait: A Case Report. [PDF]
Alhasan S +4 more
europepmc +1 more source
Burden of hemoglobinopathies and hemolytic anemias in the World Health Organization African region, 2000-2021: Findings from the Global Burden of Disease 2021 study. [PDF]
GBD 2021 Hemoglobinopathies and Hemolytic Anemias Collaborators +32 more
europepmc +1 more source

