Erythrocytic phosphatidylserine exposure and hemostatic alterations in β-thalassemia intermediate patients
M Zahedpanah, A Azarkeivan, M Aghaieepour… - …, 2014 - Taylor & Francis
Introduction Hypercoagulable state is one of the common findings in beta-thalassemia
intermedia (β-TI), particularly in splenectomized patients, with infrequent blood transfusion …
intermedia (β-TI), particularly in splenectomized patients, with infrequent blood transfusion …
Low levels of coagulation inhibitors: a high-risk thrombotic factor in thalassemic patients
Z Mousavi, S Soleymani, G Hassanshahi… - Revista Clínica …, 2020 - Elsevier
Background and aim The β-thalassemia major (β-TM) is defined as a hereditary red blood
cell (RBC)-related disease. Thrombotic events are associated with thalassemia in adult …
cell (RBC)-related disease. Thrombotic events are associated with thalassemia in adult …
[HTML][HTML] Evaluation of platelet aggregation in splenectomized beta-thalassemia major and intermedia patients
M Zahedpanah, A Azarkeivan… - Journal of Applied …, 2018 - journals.lww.com
BACKGROUND: Platelet dysfunction may be one of the pathophysiologic complications in
beta-thalassemia patients. However, the results obtained from the platelet aggregation vary …
beta-thalassemia patients. However, the results obtained from the platelet aggregation vary …
Bajos niveles de inhibidores de la coagulación: un factor de alto riesgo trombogénico en pacientes talasémicos
Z Mousavi, S Soleymani, G Hassanshahi… - Revista Clínica …, 2020 - Elsevier
Antecedentes y objetivo La β-talasemia mayor (β-TM) se define como una enfermedad
hereditaria relacionada con las células rojas sanguíneas. En los pacientes adultos, los …
hereditaria relacionada con las células rojas sanguíneas. En los pacientes adultos, los …
Comparison of Need of Transfusion and Adverse Effects before and after Splenectomy in Beta-Thalassemic Patients
AA Darzi, A Tamaddoni, MS Ramezani… - Journal of Babol …, 2012 - jbums.org
BACKGROUND AND OBJECTIVE: Thalassemia is the most common hereditary disease.
Hypersplenism and splenomegaly occur in thalassemic patients due to the hereditary defect …
Hypersplenism and splenomegaly occur in thalassemic patients due to the hereditary defect …
[PDF][PDF] http://maneytrack. maney. co. uk
K Lawson - researchgate.net
Materials and methods: Our cross-sectional study was conducted on 39 splenectomized β-TI
patients and 38 age-matched healthy controls. The mean age was 37 years. Analysis of the …
patients and 38 age-matched healthy controls. The mean age was 37 years. Analysis of the …