Results 151 to 160 of about 607,752 (259)

Hypervirulent Klebsiella pneumoniae Infections: A Systematic Review of Clinical, Microbiological, and Outcome Data From Reported Cases

open access: yesMicrobiologyOpen, Volume 15, Issue 3, June 2026.
Distribution of organ involvement in reported hypervirulent Klebsiella pneumoniae cases. Studies restricted to isolated liver abscess cases were excluded. Percentages represent the proportion of cases with documented involvement of each anatomical site among cases with available data.
Nermin Sakru   +4 more
wiley   +1 more source

How I manage luspatercept in transfusion-dependent beta-thalassemia. [PDF]

open access: yesHemasphere
Panzieri DL   +5 more
europepmc   +1 more source

Pregnancy in women with thalassemia: challenges and solutions

open access: yes, 2016
George Petrakos, Panagiotis Andriopoulos, Maria Tsironi Department of Nursing, University of Peloponnese, Sparta, Greece Abstract: Advances in treatment of thalassemia have led to the aging of thalassemic patients, and consequently concern about ...
Andriopoulos P, Petrakos G, Tsironi M
core  

Behind the splenomegaly: a parasitic twist in siblings with beta thalassemia trait. [PDF]

open access: yesBMC Pediatr
Ali A   +4 more
europepmc   +1 more source

An Investigation of Group-Based Mobile Learning on Stress, Anxiety, Depression, and Pain Among Beta-Thalassemia Major Patients: A Randomized Control Trial

open access: yes
Objective: Beta-thalassemia major (B-TM) is an inherited hematological disease that affects nearly 300 million people worldwide. This study aimed to evaluate the effects of group-based mobile learning on stress, anxiety, depression, and pain among beta ...
Mahsa Imanian   +2 more
core   +1 more source

Red blood cell membrane proteome as a reporter of disease severity, transfusion impact and genetic background in transfusion‐dependent β‐thalassaemia

open access: yesBritish Journal of Haematology, Volume 208, Issue 6, Page 1980-1992, June 2026.
Summary Omics technologies have transformed research in haemoglobinopathies, yet the proteome of RBCs remains largely unexplored in transfusion‐dependent thalassaemia (TDT). In this proteomic analysis, Red blood cell (RBC) membranes from 48 adults with TDT were compared with healthy controls.
Konstantina Theocharaki   +8 more
wiley   +1 more source

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

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

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

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