Results 91 to 100 of about 89,469 (290)
Eisenmenger syndrome: current perspectives
Research Reports in Clinical Cardiology, 2017 Heba Nashat,1–3 Aleksander Kempny,1–3 Colm McCabe,1 Laura C Price,1–3 Carl Harries,1 Rafael Alonso-Gonzalez,1–3 Michael A Gatzoulis,1–3 Stephen J Wort,1–3 Konstantinos Dimopoulos1–3 1Adult Congenital Heart Centre
Nashat H +8 more
doaj
Frontiers in Cardiovascular MedicineBackground and aimsProgress in cardiology has extended the lifespan of patients with congenital heart defects (CHD). Cyanotic patients are exposed to typical diseases of adulthood, including atherosclerosis. Rheological changes typical of cyanosis affect
Sonia Alicja Nartowicz +7 more
doaj +1 more source
Cardiovascular Health in Women—Across the Lifespan
Clinical Endocrinology, EarlyView.ABSTRACT Cardiovascular disease (CVD) remains the leading cause of mortality and morbidity among women worldwide. However, CVD continues to be perceived as a predominantly male issue. CVD in women therefore remains understudied, underrecognized and undertreated.
Jaya Chandrasekhar +5 more
wiley +1 more source
Atrial septal defect - Secundum type with eisenmenger's syndrome: A rare occurrence
Journal of Indian College of Cardiology, 2020 Atrial septal defect is the second most common congenital heart disease in adults.[1] Many experienced physicians make a great effort in diagnosing this heart disease. However, many patients still stand behind the curtain, undiagnosed.
Rohit Manoj Jacob, Manjiri Naik
doaj +1 more source
Cor triatriatum dexter: A rare cause of childhood cyanosis
Annals of Pediatric Cardiology, 2012 Cor triatriatum dexter is a rare congenital heart anomaly where the right atrium is divided into two chambers by a membrane. We report a boy who had persistent mild cyanosis and diagnosed to have cor triatriatum dexter with secundum atrial septal defect ...
A. Zainudin., K. G. Tiong, S. A. Mokhtar
semanticscholar +1 more source
Incidental pulmonary arteriovenous malformation
Journal of Hospital Medicine, EarlyView.
Mallory A. Von Lotten +2 more
wiley +1 more source
Cell Proliferation, EarlyView.The endoplasmic reticulum membrane protein complex (EMC) is an evolutionarily conserved, multi‐subunit transmembrane protein complex crucial to membrane protein biogenesis and cellular protein quality control. This review systematically examines the structure, functions and disease‐associated regulatory mechanisms of EMC across multiple organ systems ...
Yan Qiao +6 more
wiley +1 more source
Comparing the effect of using normal saline, N-acetyl cysteine and not using them in endotracheal tube suction on physiologic parameters and the amount of secretions in intubated patients under mechanical ventilation [PDF]
, 2014 Aims: Today a large number of patients hospitalized in Intensive Care Unit need mechanical ventilation via an artificial air way. Since these patients have endotracheal tube, endotracheal suctioning is necessary for increasing oxygenation, cleaning the ...
Akbaryan Deheki, N. +6 more
core
Early postoperative interventional ASD-closure for severe atrial right to left shunt in a neonate with common arterial trunk [PDF]
, 2013 Although closure of an atrial septal defect (ASD II) with an occluding device in the first year of life is not a routine procedure, it is a feasible treatment, even in neonates.
Dilber, Daniel +2 more
core +1 more source
Developmental Medicine &Child Neurology, EarlyView.This systematic review identifies and categorizes the spectrum of non‐epileptic paroxysmal events in Rett syndrome. Respiratory disturbances, behavioural episodes, and motor events were the most commonly reported. Improving clinician awareness and diagnostic clarity is key to avoiding unnecessary treatment and enhancing quality of life for individuals ...
Natasha Bhatti, Daniel E. Lumsden
wiley +1 more source