Hematological indices and cytokine profiles in heterozygous beta-thalassemia.
19/11/2025
Abstract Introduction β-thalassemia is defined by a reduction or total absence of β-globin chain synthesis in hemoglobin, causing hemolytic anemia.
Abstract We present the case of a 35-year-old female patient with a previous diagnosis of paroxysmal nocturnal hemoglobinuria (PNH), treated…
Read more →Abstract Introduction β-thalassemia is defined by a reduction or total absence of β-globin chain synthesis in hemoglobin, causing hemolytic anemia.
Simplified summary Title: Are direct oral anticoagulants (a type of “blood thinner”) better than traditional anticoagulants for treating pulmonary thromboembolism