The shape shifting story of reticulocyte maturation

E Ovchynnikova, F Aglialoro, M Von Lindern… - Frontiers in …, 2018 - frontiersin.org
The final steps of erythropoiesis involve unique cellular processes including enucleation
and reorganization of membrane proteins and the cytoskeleton to produce biconcave …

[HTML][HTML] Red blood cell alloimmunisation in transfusion-dependent thalassaemia: a systematic review

M Franchini, GL Forni, G Marano, M Cruciani… - Blood …, 2019 - ncbi.nlm.nih.gov
Background Chronic red blood cell transfusion is the first-line treatment for severe forms of
thalassaemia. This therapy is, however, hampered by a number of adverse effects, including …

[HTML][HTML] Prevalence of red blood cell major blood group antigens and phenotypes among Omani blood donors

AZ Al-Riyami, A Al-Marhoobi, S Al-Hosni… - Oman Medical …, 2019 - ncbi.nlm.nih.gov
Objectives Most literature on the frequencies of red blood cell (RBC) phenotypes are
published in Europeans and Africans countries, with the frequencies in the Omani …

Frequency of red blood cell alloimmunization in patients with sickle cell disease in Palestine

F Samarah, MA Srour, D Yaseen… - Advances in …, 2018 - Wiley Online Library
Background. Transfusion of red blood cells (RBC) is an essential therapeutic tool in sickle
cell disease (SCD). Repeated RBC transfusions can cause alloimmunization which causes …

Blood donation barriers and facilitators of Sub‐Saharan African migrants and minorities in Western high‐income countries: A systematic review of the literature

EF Klinkenberg, EMJ Huis In't Veld… - Transfusion …, 2019 - Wiley Online Library
Objectives The present study aimed to gain more insight into, and summarise, blood
donation determinants among migrants or minorities of Sub‐Saharan heritage by …

Red cell alloimmunization and autoimmunization among sickle cell disease and thalassemia patients in jazan province, Saudi Arabia

AJ Halawani, AA Mobarki, AH Arjan… - … Journal of General …, 2022 - Taylor & Francis
Purpose Sickle cell disease (SCD) and thalassemia are common inherited blood disorders
in Saudi Arabia, especially in Jazan Province. Patients with these disorders require multiple …

Red Blood Cell Alloimmunization and Autoimmunization in Blood Transfusion‐Dependent Sickle Cell Disease and β‐Thalassemia Patients in Al‐Ahsa Region, Saudi …

FA Kuriri, A Ahmed, F Alanazi, F Alhumud… - Anemia, 2023 - Wiley Online Library
Introduction. The risk of developing transfusion‐related complications, especially
alloimmunization, is an ongoing concern for transfusion‐dependent patients. It is important …

The value of transfusion of phenotyped blood units for thalassemia and sickle cell anemia patients at an academic center

S Hindawi, M Badawi, R Elfayoumi, T Elgemmezi… - …, 2020 - Wiley Online Library
BACKGROUND Blood transfusion is the first‐line treatment for patients with thalassemia and
many sickle cell patients. However, cases of unregulated blood transfusion are shown to …

Iron Overload in Patients With Heavily Transfused Sickle Cell Disease—Correlation of Serum Ferritin With Cardiac T2* MRI (CMRTools), Liver T2* MRI, and R2-MRI …

S Alkindi, V Panjwani, S Al-Rahbi, K Al-Saidi… - Frontiers in …, 2021 - frontiersin.org
The treatment of sickle cell disease (SCD) is mainly supportive, except for a minority, who
receive bone marrow transplantation (BMT). Serum ferritin (SF) is routinely available but is …

The Rh blood group system and its role in alloimmunization rate among sickle cell disease and sickle thalassemia patients in Iran

MA Jalali Far, A Oodi, N Amirizadeh… - … Genetics & Genomic …, 2021 - Wiley Online Library
Introduction The alloimmunization following blood transfusion can be life‐threatening. The
Rh alloantibodies are one of the most common causes contributing to alloimmunization. This …