Results 131 to 140 of about 158,916 (259)
Transfusion Medicine, EarlyView.Abstract Objective This study aimed to analyse the distribution and demand patterns of antigen‐negative red blood cells (RBCs) in Shandong Province, China (2022–2024), with a focus on ABO blood groups and clinically significant antigens. The research was designed to provide rigorous data for advancing precision transfusion protocols and to establish a ...
Aiping Zhao +7 more
wiley +1 more source
Case report: Rethinking NGS analysis in diagnosing Diamond-Blackfan anemia syndrome
Frontiers in GeneticsDiamond-Blackfan anemia syndrome (DBAS) is a rare inherited bone marrow failure (BMF) syndrome characterized by erythroid aplasia, congenital malformations, and cancer predisposition.
Panayiota L. Papasavva +7 more
doaj +1 more source
The Perceived Role of God in Health and Illness: the Experience of Javanese Mothers Caring for a Child with Thalassemia [PDF]
, 2011 Thalassemia is recognized as one of the major health problem in Indonesia. It is estimated that about 10% of Indonesian population are carrier of the mutated gene. Nevertheless Thalassemia is not well-understood by communities.
Widayanti, C. G. (Costrie)
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Safety and tolerability of amustaline/glutathione pathogen‐reduced red blood cells in neonatal rats
Transfusion, EarlyView.Abstract Background Amustaline (S‐303)/glutathione (GSH) pathogen‐reduced red blood cells (PR‐RBCs) are in development for all adult and pediatric RBC transfusion indications, including neonates and infants. A neonatal rat model evaluated the safety and tolerability of PR‐RBCs during growth and maturation. Study Design and Methods Repeated transfusions
Anne North +3 more
wiley +1 more source
Conformational lock and thermal inactivation kinetics of Euphorbia amine oxidase [PDF]
The kinetics of thermal inactivation of copper-containing amine oxidase from euphorbia latex (ELAO) were studied in a 100-mM sodium phosphate buffer, pH 7, using cadavarine as the substrate.
امانی, مجتبی +6 more
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Vox Sanguinis, EarlyView.Abstract Background and Objectives Adequate representation of donors from diverse ancestral populations in blood, stem cell and organ transplantation is critical to ensuring equitable access to these lifesaving therapies. Because of population‐level differences in genetic markers, patients from racialized groups may have unique transfusion and ...
Bonnie Lu +9 more
wiley +1 more source
Mediterranean Journal of Hematology and Infectious Diseases, 2014 The erythrocyte, devoid of nucleus, mitochondria,ribosomes and other organelles, has no capacity for cell replication, protein synthesis, or oxidative phosphorylation.
SOPHIA DELICOU +5 more
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The Longitudinal Effect of APOL1 Risk Alleles on Sickle Cell Anemia‐Associated Kidney Function
American Journal of Hematology, Volume 101, Issue 6, Page 1341-1350, June 2026.ABSTRACT Progressive kidney injury is a major cause of morbidity and mortality in sickle cell anemia (SCA). The high risk APOL1 G1/G2 variants contribute to the development of kidney disease in individuals of African ancestry, including those with SCA.
Sara R. Rashkin +7 more
wiley +1 more source
International Journal of Laboratory Hematology, Volume 48, Issue 3, Page 521-530, June 2026.ABSTRACT Hematologic emergencies are urgent health conditions which result in significant mortality and morbidity unless timely therapeutic measures are taken. Therapeutic success depends on their timely and accurate recognition by hematology laboratory services.
Ganna Shestakova +2 more
wiley +1 more source
Deletional a-thalassemia 1 gene detection and hematological analysis in carrier with β-thalassemia
Journal of Associated Medical Sciences, 2012 There are high prevalence of β-thalassemia and α-thalassemia in the upper Northern Thailand. Thus, the interaction between β-thalassemia and α-thalassemia can be occurred.
Sitthichai Panyasai
doaj