Results 141 to 150 of about 71,295 (266)

A genetic risk score based on BCL11A and HBS1L‐MYB variants predicts clinical severity in Brazilian sickle cell anaemia patients

open access: yesBritish Journal of Haematology, Volume 208, Issue 6, Page 2203-2211, June 2026.
Summary Individuals with sickle cell anaemia (SCA) exhibit significant clinical heterogeneity influenced by several factors, especially fetal haemoglobin (HbF) levels. Variations in adult HbF levels are partly explained by the co‐inheritance of genetic variants that regulate globin expression.
Gabriela S. Arcanjo   +13 more
wiley   +1 more source

Thalassemia carrier screening in siblings of thalassemia major patients by HbA2 estimation

open access: yes, 2017
Objective: Thalassemia carrier screening in siblings of thalassemia major patients by HbA2 estimation. Methods: This prospective, cross-sectional study was conducted at thalassemia welfare society of JK Lon Hospital, Kota.
Sharma, Gopikishan   +2 more
core  

Evaluation of heart rate variability in pediatric patients with beta thalassemia major: Cross-sectional study. [PDF]

open access: yesWorld J Clin Pediatr
Sorour EA   +5 more
europepmc   +1 more source

Incidence, Risk Factors, and Outcome of Transplant‐Related Intra‐Cranial Hemorrhage in Pediatric Thalassemia Major Patients

open access: yesPediatric Transplantation, Volume 30, Issue 6, June 2026.
Intracranial hemorrhage (ICH) occurred in 4.7% of pediatric patients after matched‐related bone marrow transplantation for thalassemia major, predominantly in the early post‐transplant period. Older age at transplant is a significant predictor for ICH.
Aliya Batool   +12 more
wiley   +1 more source

Clinical and Genetic Pattern of β-Thalassemia Major in East Java, Indonesia. [PDF]

open access: yesJ Blood Med
Romadhon PZ   +9 more
europepmc   +1 more source

Addressing racial disparities in representation across blood, stem cell and organ and tissue donor pools

open access: yesVox Sanguinis, Volume 121, Issue 6, Page 710-721, June 2026.
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

Lived experiences of Iranian parents of beta-thalassemia children

open access: yes, 2017
Aziz Shahraki-vahed,1 Mohammadreza Firouzkouhi,1 Abdolghani Abdollahimohammad,1 Jamile Ghalgaie2 1Department of Medical Surgical, Faculty of Nursing and Midwifery, Zabol University of Medical Science, Zabol, Iran; 2Emam Khomeni Hospital, Zabol University
Shahraki-vahed A   +3 more
core  

Reduced number of endothelial progenitor cells in adult patients with beta thalassemia major. [PDF]

open access: yesAnn Hematol
Goldberg I   +9 more
europepmc   +1 more source

Antioxidant Effects of CoQ10 in Transfusion-Dependent β-Thalassemia Major Patients: Implications for Ferroptosis-Related Pathways

open access: yes
Kiavash Fekri,1 Mohammad Mehdi Mirforoughi,2 Yaser Salehinajafabadi,3 Hadi Raeisi Shahraki,4 Raziyeh Ershadi,5 Shima Rahmati1 1Cancer Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran; 2Shahid Beheshti University of Medical ...
Ershadi R   +5 more
core  

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