Results 151 to 160 of about 8,109 (242)

What is the best approach to blood transfusion in sickle cell disease? A scientometric analysis and literature review

open access: yesTransfusion Medicine, Volume 36, Issue 3, Page 211-221, June 2026.
Abstract Background Blood transfusion remains a cornerstone in the management of sickle cell disease (SCD); however, it is frequently complicated by red cell alloimmunisation. A significant debate persists within the scientific community regarding the optimal strategy to mitigate this risk: the traditional, pragmatic approach of serologic phenotyping ...
Christiane Ruffato Carminati   +6 more
wiley   +1 more source

Genetic diversity in RHD and RHCE genes among a selected Kenyan blood donor population

open access: yesTransfusion, Volume 66, Issue 6, Page 1192-1202, June 2026.
Abstract Background Serologic typing for ABO and RhD is standard in transfusion services, with extended serology and genotyping performed to reduce red cell alloimmunization risk. In Kenya, RH typing is limited to RhD, and genotyping is unavailable. This study used RHD/RHCE genotyping to predict phenotypes and their distribution in a Kenyan blood donor
Sandra A. Sowah   +8 more
wiley   +1 more source

Evaluation of β-thalassemias in the premarital hemoglobinopathy screening program: A retrospective study

open access: yes
Objective: To retrospectively evaluate B-thalassemias in the premarital hemoglobinopathy screening program in primary care. Methods: The retrospective study was carried out in Bursa Uludag University Family Health Center in Turkey between 1-30 September ...
Goktas, Olgun
core   +1 more source

Study of the Prevalence of Cytomegalovirus in Children with Malignancy in Southwestern Iran from 2016-2023 [PDF]

open access: yesIranian South Medical Journal
Background: Cytomegalovirus (CMV) infection is one of the most common infections worldwide. This infection is especially dangerous for people with weakened immune systems and patients who have had organ transplants.
Arash Alghasi   +5 more
doaj  

Hemoglobinopathies

open access: yes, 2019
Hereditary hemoglobin disorders with thalassemia and sickle-cell anemia are the most common monogenic diseases in the world. It is estimated that about 1-5% of the global population is the carriers of a genetic thalassemia mutation. Hemoglobinopathies are among the most common hereditary blood diseases also in Turkey and are an important health problem
Arpacı, Abdullah   +2 more
openaire   +1 more source

Using unmanned aerial vehicles (drones) to improve access to blood in low‐ and middle‐income countries: Current challenges and opportunities

open access: yesVox Sanguinis, Volume 121, Issue 6, Page 700-709, June 2026.
Abstract Blood transfusion is life‐saving for patients in emergencies, but low‐ and middle‐income countries (LMICs) often face a severe shortage of banked blood. Establishing blood banks in rural areas presents substantial logistical and economic challenges for many LMICs.
Suvro Sankha Datta   +4 more
wiley   +1 more source

Real‐world evidence supports the safety and efficacy profile of luspatercept in clinically complex and heavily iron‐overloaded patients

open access: yes
British Journal of Haematology, Volume 208, Issue 6, Page 2320-2325, June 2026.
Barbara Gianesin   +29 more
wiley   +1 more source

Aging with Thalassemia and Sickle Cell Disease: A Gerontological Model of Accelerated Multimorbidity and Function-Centered Care Beyond Midlife. [PDF]

open access: yesMediterr J Hematol Infect Dis
Delicou S   +14 more
europepmc   +1 more source

Evaluation of surgical evacuation of the uterus for abortion and management of miscarriage in patients with sickle cell disease: A multicentre UK study

open access: yes
British Journal of Haematology, Volume 208, Issue 6, Page 2307-2310, June 2026.
Sonia Wolf   +5 more
wiley   +1 more source

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