Results 131 to 140 of about 53,686 (285)

Hypomorphic ATP11c is a novel regulator of decreased efficacy of transfused red blood cells in humans and mice

HemaSphere, Volume 10, Issue 1, January 2026.
Abstract Chronic red blood cell (RBC) transfusion sustains patients with diverse hematologic disorders, but repeated transfusion leads to iron overload and alloimmunization. Reducing transfusion burden requires identifying donor units that circulate more effectively after storage, yet determinants of this variability remain incompletely defined.
James C. Zimring, Ariel M. Hay, Monika Dzieciatkowska, Daniel Stephenson, Zachary B. Haiman, Steven Kleinman, Philip J. Norris, Michael P. Busch, Nareg Roubinian, Elisa Fermo, Paola Bianchi, Gregory R. Keele, Grier P. Page, Angelo D'Alessandro   +13 more
wiley   +1 more source

GlutathioneS-transferase gene polymorphism: Relation to cardiac iron overload in Egyptian patients with Beta Thalassemia Major [PDF]

, 2015
Galila M. Mokhtar, Eman M. Sherif, Nevin M. Habeeb, Abeer A. Abdelmaksoud, Eman A. Elghoroury, Ahmed S. Ibrahim, Enas M. Hamed   +6 more
openalex   +1 more source

Frequencies of Beta Thalassemia Mutations Show Different Pattern in Bannu Region than Other Parts of Pashtun Population in Khyber Pakhtunkhwa Province Pakistan

, 2021
Shoaib Ur Rehman, Muhammad Shakeel, Maimoona Azam, Sadaf Akhtar, Ziaullah, Rauf Niazi   +5 more
openalex   +2 more sources

Delta beta thalassemia [PDF]

American Journal of Hematology, 2019
openaire   +2 more sources

Erythropoiesis in health and disease: Distinguishing defective and ineffective erythropoiesis

HemaSphere, Volume 10, Issue 1, January 2026.
Abstract Erythropoiesis is a finely regulated process ensuring continuous red blood cell production to maintain oxygen delivery. Disruptions in this process give rise to defective erythropoiesis, characterized by impaired lineage commitment and progenitor development, and ineffective erythropoiesis (IE), marked by expansion of erythroid progenitors ...
Sara El Hoss, Maria A. Lizarralde‐Iragorri, Thiago Trovati Maciel, Olivier Hermine   +3 more
wiley   +1 more source

Factors associated with continuing emergence of β-thalassemia major despite prenatal testing: a cross-sectional survey

International Journal of Women's Health, 2017
Haleama Al Sabbah,1 Sarah Khan,1 Abdallah Hamadna,2 Lamia Abu Ghazaleh,2 Anwar Dudin,2 Bashar Adnan Karmi3 1College of Natural and Health Sciences, Zayed University, Dubai, UAE; 2Faculty of Medicine, An-Najah National University, Nablus, Palestine ...
Al Sabbah H, Khan S, Hamadna A, Abu Ghazaleh L, Dudin A, Karmi BA   +5 more
doaj  

Association of IL28B Polymorphisms With Hepatitis C Susceptibility in Southern Iran's β‐Thalassemia Population: A Cross‐Sectional Study

Health Science Reports, Volume 9, Issue 1, January 2026.
ABSTRACT Background and Aims Thalassemia is a hereditary hematological condition which interferes with the production of hemoglobin (Hb). Patients with thalassemia require regular blood transfusion, which makes them highly susceptible to pathogens, and especially viral pathogens.
Fatemeh Askari, Masoud Kargar, Zeinab Deris Zayeri, Mohammad Ali Jalalifar, Bijan Keikhaei, Gholam Abbas Kaydani   +5 more
wiley   +1 more source

Protective Effects of Selenium in Patients with Beta-Thalassemia Major [PDF]

, 2020
ajand aboutalebi, Abolghasem Jouyban, Hadi Chavoshi, Aliakbar Movassaghpour Akbari, Elnaz Shaseb, Parvin Sarbakhsh, Saba Ghaffary   +6 more
openalex   +1 more source

The Role of Viral and Bacterial Infections in the Etiology of Behçet's Disease

Journal of Clinical Laboratory Analysis, Volume 40, Issue 1, January 2026.
Bacterial and viral pathogens may play a key role in Behçet's disease (BD) pathogenesis by triggering autoimmunity, molecular mimicry, or microbiome disruption. These infectious agents could initiate inflammatory pathways, contributing to BD's diverse clinical manifestations.
Mohsen Moghoofei, Hamid Pajavand, Razieh Shahbazi, Marzieh Rezaei, Elahe Taki   +4 more
wiley   +1 more source

Pre-Natal Diagnosis of beta – Thalassemia by Chorionic Villous Sampling

Journal of Rawalpindi Medical College, 2009
Background: To promote the utility of Chorionic Villous Sampling (CVS) for pre-natal diagnosis of beta thalassemia in at risk population and to highlight its demographic area distribution and effect of consanguinity.
Shazia Syed,
doaj