Results 111 to 120 of about 22,488 (223)
Splenic contraction associated with sudden, transient hypotension and sympathoexcitation in humans
Experimental Physiology, EarlyView.Abstract The spleen is traditionally recognised for its roles in immunity and blood filtration, and it is known to contract and release stored erythrocytes in hypoxic conditions. Recent findings suggest that the spleen may also contribute to cardiovascular regulation.
Angelica Lodin‐Sundström +5 more
wiley +1 more source
Clinical Interventions in Aging, 2013 Xuguang Qin,1 Weiguo Xiong,1 Enben Guan,2 Chunpeng Lu1 1Department of Cardiology, First Affiliated Hospital of Tsinghua University, Beijing, People’s Republic of China; 2Department of Pediatric, The Affiliated Hospital of Qingdao Medical College ...
Qin X, Xiong W, Guan E, Lu C
doaj
The Journal of Physiology, EarlyView.Abstract figure legend Arboviruses induce virus‐specific alterations in placental structure and functional markers. Chikungunya virus (CHIKV) exposure was associated with reduced syncytiotrophoblast and syncytial knot areas, increased cytotrophoblast proliferation (Ki‐67) and thyroid transporter (MCT8) expression, reduced protective (P‐gp and BCRP ...
Cherley B. V. Andrade +13 more
wiley +1 more source
Journal of Applied Polymer Science, Volume 143, Issue 36, September 20, 2026.Curcumin encapsulation in nanomicelles coupled with a machine learning–guided model for predicting its release profile. ABSTRACT This work, leveraging machine‐learning algorithms, focuses on the design and in vitro evaluation of oil‐in‐water surfactant‐based nanomicelles as a novel curcumin formulation with comparable cytotoxic effects against MCF‐7 ...
Abbas Rahdar +3 more
wiley +1 more source
A rare coronary anomaly as a possible cause of ventricular tachycardia [PDF]
Arch Cardiol Mex, 2022 Cuevas-Pérez J +3 more
europepmc +1 more source
American Journal of Medical Genetics Part A, Volume 200, Issue 9, Page 2140-2150, September 2026.ABSTRACT Multiple Acyl‐CoA Dehydrogenase Deficiency (MADD) is an autosomal recessive inborn error of metabolism caused by biallelic pathogenic variants in one of three known genes: ETFA, ETFB, and ETFDH. It can cause multisystem dysfunction, including cardiomyopathy in severe cases.
Yutaka Furuta +17 more
wiley +1 more source
Congenital Coronary Artery Anomalies
Journal of the Korean Society of RadiologySee the article, “Type 4 Dual Left Anterior Descending Artery: A Case Report of a Rare Congenital Coronary Anomaly”, in volume 85 on page 428-433 (https://doi. org/10.3348/ jksr.2022.0147).
openaire +3 more sources
Congenital anomalies of the coronary arteries.
Revista portuguesa de cardiologia, 2018 Congenital coronary artery anomalies are modifications of their origin, course or structure and its incidence varies between 0,2 and 5,6% of the general population. Although the majority is asymptomatic, they are the second leading cause of sudden cardiac death in young athletes. The aim of this study is to highlight the main anomalies with hemodynamic
Silva, Andreia +2 more
openaire +2 more sources
Pregnancy, Volume 2, Issue 5, September 2026.Abstract Introduction Pregnant people with congenital heart disease (CHD) are a growing patient population in obstetrics, yet evidence on the risk for severe maternal morbidity (SMM) has largely been limited to studies that lack specificity for CHD. We conducted this study to demonstrate the utility of distributed data networks for obstetric research ...
Elizabeth B. Sherwin +11 more
wiley +1 more source
Detecting a subendocardial infarction in a child with coronary anomaly by three-dimensional late gadolinium enhancement MRI using compressed sensing. [PDF]
Radiol Case Rep, 2021 Suekuni H +9 more
europepmc +1 more source