Results 131 to 140 of about 607,752 (259)
Therapeutic Value of Silymarin as Iron Chelator in Children with Beta Thalassemia with Iron Overload
Beta thalassemia is an inherited hemoglobin disorder resulting in chronic hemolytic anemia. The most common treatment for thalassemia is blood transfusion which is necessary to provide the patients with healthy red blood cells containing normal ...
adel abd elhaleim hagag
doaj
Genetic analysis of beta-thalassemia major and beta-thalassemia intermedia in Brazil
The development of methodologies to identify the molecular lesions responsible for different types of beta-thalassemia has made it possible to correlate these data with clinical and hematological severity.
Kerbauy, J +7 more
core
OBJECTIVE: To determine the frequency of beta thalassemia trait in pregnant anemic patients attending Khyber Teaching Hospital, Peshawar, Pakistan. METHODS: This descriptive cross sectional study was conducted in Gynecology and Obstetrics Department of ...
Maimoona Qadir, Sohail Amir
doaj
ABSTRACT Objectives Immune thrombocytopenia (ITP) during pregnancy presents unique management challenges. This study represents the first analysis of ITP outcomes during pregnancy in Qatar, aiming to assess maternal and neonatal outcomes at a tertiary care center.
Sara Elkorashi +10 more
wiley +1 more source
openaire +1 more source
Impaired switching from fetal hemoglobin (HbF) to adult globin gene expression leads to hereditary persistence of fetal hemoglobin (HPFH) in adult life.
Gaudino, Sara
core
ABSTRACT Background and Aim Endogenous erythropoietin (EPO) deficiency has been associated with anemia in patients with type 2 diabetes mellitus (T2DM) and renal injury. The purpose of this study was to characterize EPO levels and anemia in Vietnamese patients with T2DM and chronic kidney disease (CKD).
Nguyen Ngoc Anh +3 more
wiley +1 more source
American Journal of Hematology, Volume 101, Issue 6, Page 1196-1200, June 2026.
Bo A. Wan +7 more
wiley +1 more source
ABSTRACT Prior surveys of chronic automated red blood cell exchange (RCE) for patients with sickle cell disease (SCD) have identified considerable procedural variability, especially with the use of isovolemic hemodilution red blood cell exchange (IHD‐RCE).
Jennifer M. Jones +27 more
wiley +1 more source
G‐CSF for Mobilizing CD34+ Cells in Individuals With SCD: A Word of Caution
American Journal of Hematology, Volume 101, Issue 6, Page 1178-1181, June 2026.
Akshay Sharma +17 more
wiley +1 more source

