Results 131 to 140 of about 872,130 (197)
Cerebral Blood Transit in Sickle Cell Anemia
ABSTRACT Background Sickle cell anemia (SCA) patients upregulate cerebral blood flow to compensate for decreased arterial oxygen content. Such hyperemic conditions can manifest as venous hyperintense signal on arterial spin labeling (ASL) MRI, which may reflect faster capillary blood transit, altered oxygen extraction fraction (OEF), and infarct risk ...
Wesley T. Richerson +10 more
wiley +1 more source
Extramedullary haematopoiesis in patients with transfusion dependent β-thalassaemia (TDT): a systematic review. [PDF]
A Subahi E +7 more
europepmc +1 more source
Smart Design: Integrating Artificial Intelligence and Gene Editing for Advanced mRNA Therapeutics
The challenges of mRNA therapy and the application of artificial intelligence and gene editing in the field of mRNA drugs. ABSTRACT Artificial intelligence (AI) and gene editing are increasingly being applied to the design and evaluation of mRNA therapeutics.
Haixing Shi +11 more
wiley +1 more source
Extramedullary haematopoiesis presenting as an adnexal mass in a patient with β-thalassaemia. [PDF]
Filippi V +3 more
europepmc +1 more source
An Italian family in which heterocellular hereditary persistence of fetal haemoglobin (HPFH) interacts with both β+- and δβ-thalassaemia is described.
Care A. +9 more
core
DAMPs, PAMPs, and Alarmins: From Mechanism to Therapy
This review synthesizes the expanding biology of PAMPs and DAMPs, from their molecular sources and sensing mechanisms to regulatory networks that govern inflammation and homeostasis. Spanning from classical immune activation to trained immunity and interorgan communication, we highlight the interplay between PAMPs and DAMPs and their context‐dependent ...
Xuanxuan Yu +6 more
wiley +1 more source
Hepcidin Levels in Multi Transfused β Thalassemia Major Patients
Background: To determine and compare the serum hepcidin levels and conventional markers of iron status in patients of β- thalassaemia major with controls.
Muhammad Jawad
doaj
A systematic review on thalassaemia screening and birth reduction initiatives cost to success [PDF]
Introduction: Thalassaemia has been prevalent with high morbidity and mortality rates since 1925. Although there is a lack of systematic review on the costs of prevention that has yielded reductions in thalassaemia prevalence, this review will show a ...
Abd Rahim, Azrin Syahida +2 more
core
ABSTRACT Mirror syndrome is a rare maternal–fetal condition associated with fetal hydrops and a high risk of adverse maternal and fetal perinatal outcomes. Its diagnosis is challenging due to the lack of standardized diagnostic criteria and its clinical and biochemical overlap with preeclampsia.
Riccardo Tudisco +5 more
wiley +1 more source
Impaired neutrophil extracellular trap formation in β-thalassaemia/HbE. [PDF]
Thubthed R +7 more
europepmc +1 more source

