Results 151 to 160 of about 607,752 (259)
Osteoporosis risk in alpha and beta thalassemia: An age- and sex-specific retrospective cohort study. [PDF]
Hsu YS, Tseng SC, Chao TF, Chen KH.
europepmc +1 more source
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]
Panzieri DL +5 more
europepmc +1 more source
Pregnancy in women with thalassemia: challenges and solutions
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]
Ali A +4 more
europepmc +1 more source
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
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]
Sorour EA +5 more
europepmc +1 more source
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]
Goldberg I +9 more
europepmc +1 more source

