Results 31 to 40 of about 859,055 (185)

Differences in sex, angiographic frequency, and parameters in patients with coronary artery anomalies: single-center screening of 25 368 patients by coronary angiography

, 2013
Background: Although the prevalence of coronary artery anomalies varies in different series, the precise population frequency is unknown. Materials and methods: The medical records of all patients who underwent coronary angiography between January
Akpinar, Ibrahim, Mustafa Aydin, Kucuk, Emrah, Sibel Kiran, Yusuf Cemil Gursoy, Dogan, Siat M., Muhammet Rasit Sayin, Sayin, Muhammet R., Emrah Kucuk, Dogan, Sait M., Kiran, Sibel, Turgut Karabag, Gursoy, Yusuf C., Karabag, Turgut, Aydin, Mustafa, Sait Mesut Dogan, Ibrahim Akpinar   +16 more
core   +1 more source

Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT LRP1 encodes the low‐density lipoprotein (LDL) receptor‐related protein 1 (LRP1), a transmembrane protein involved in endocytosis and activation of multiple signaling pathways. LRP1 variants have been implicated in the pathogenesis of congenital heart defects (CHD), Alzheimer's disease, and neurodevelopmental disorders (NDD).
Alyssa L. Rippert, Gudny Anna Arnadottir, Laura Bedinger, Nicola Brunetti‐Pierri, Jennifer Cech, Xin Chen, Yanmin Chen, Erika Chick, Sarah Dyack, Madeleine Franchi, Tanja Frey, David Genevieve, Ian Glass, Jorge Granadillo, Kelly A. Keener, Sara B. MacKay, Paige McDunnah, Vinod K. Misra, Kristin G. Monaghan, Sureni V. Mullegama, Cristina Peduto, Leia Peterman‐Prather, Anita Rauch, Cherith Somerville, Kari Stefansson, Katharina Steindl, Patrick Sulem, Telma Sulem, Pamela Trapane, Roberta Zeuli, Samuel Zinner, Kosuke Izumi   +31 more
wiley   +1 more source

The caveats in the diagnosis of anomalous origin of left coronary artery from pulmonary artery (ALCAPA) [PDF]

, 2010
Anomalous origin of left coronary artery from pulmonary artery (ALCAPA) is an infrequent, well described, but important anomaly of the coronary origin. Early diagnosis and prompt surgical treatment of the disease can be life saving. However, there are
Varghese, M.J., Kothari, Shyam S.
core  

Systematic review of the clinical effectiveness and cost-effectiveness of 64-slice or higher computed tomography angiography as an alternative to invasive coronary angiography in the investigation of coronary artery disease [PDF]

, 2008
Objectives: To assess the clinical effectiveness and cost-effectiveness, in different patient groups, of the use of 64-slice or higher computed tomography (CT) angiography, instead of invasive coronary angiography (CA), for diagnosing people with ...
Cummins, E., Fraser, Cynthia Mary, Walker, S., Jia, Xueli, Cook, Jonathan Alistair, Hillis, Graham S., Waugh, N., Mowatt, Graham   +7 more
core   +3 more sources

Rheumatic valvular heart disease combined with woven coronary artery: a case report

Journal of Cardiothoracic Surgery, 2020
Background Woven coronary artery (WCA) is an extremely rare congenital anomaly in which a part of epicardial coronary artery is divided into thin channels, that twist along the axis of the coronary arteries and then merge again as the main coronary lumen.
Zhengjiang Liu, Yueliang Li
doaj   +1 more source

Coronary artery anomalies and variants among adult patients undergoing coronary angiography in Azadi heart center, Duhok/Iraq

Advanced Medical Journal, 2022
Background: Congenital coronary artery anomalies are rare among general population and are usually asymptomatic. And diagnosed accidentally during coronary angiography.
Ameel Toma Yaqo, Hashim Ahmed Sharaf, Mousa Haji Ahmed   +2 more
doaj   +1 more source

Systematic Cardiac Phenotyping of Patients With Copy Number Variants in the 15q11.2 Breakpoint 1 to Breakpoint 2 Region: A Retrospective Cohort Study From Nine Pediatric Cardiac Centers

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Microdeletions impacting 15q11.2 breakpoint (BP) 1 to BP2, adjacent to the Prader–Willi critical region, have previously described neuropsychiatric associations, with potential low penetrance presentations of congenital heart disease (CHD) also identified.
Morgan B. Wright, Maria B. Padua, Lindsey R. Helvaty, Kim L. McBride, Gabrielle Geddes, Vidu Garg, Seema R. Lalani, Stephanie Burns Wechsler, Jennelle C. Hodge, Benjamin J. Landis, Stephanie M. Ware   +10 more
wiley   +1 more source

Aortic valve disease: Novel animal models for advancing our understanding of the underlying mechanisms

Animal Models and Experimental Medicine, EarlyView.
Due to the complex pathophysiology of aortic valve disease (AVD) and the resulting lack of effective pharmacotherapy, existing animal models are valuable research tools, but each has its own strengths and limitations. This review systematically surveys the major AVD models, compares their induction methods, pathological features, advantages and ...
Liya Hou, Xue Liu, Wangxing Hu, Xianbao Liu, Wei Zhu   +4 more
wiley   +1 more source

Coronary artery grafting in infants [PDF]

, 2009
Coronary artery bypass grafting (CABG) with cardiac vale repair is an uncommon surgery in infants. CABG is technically demanding in infants due to the small size not only of the coronary arteries but also the potential graft arteries.
Menon, Rajgopal, Zacharias, S., Maskari, Salim, Valliathu, J.   +3 more
core  

Double Left Anterior Descending Coronary Artery Originating from Left Main Coronary Stem and Right Coronary Artery [PDF]

Journal of Cardiovascular and Thoracic Research, 2013
Double left anterior descending coronary artery originating from left main coronary stem and right coronary artery is a rare congenital coronary anomaly.
Fariborz Akbarzadeh, Sepide Shadravan, Maryam Ghorbanian, Reza Piri, Mohammad Naghavi-Behzad   +4 more
doaj   +1 more source