Results 81 to 90 of about 59,678 (227)

Heart failure and sudden cardiac death in heritable thoracic aortic disease caused by pathogenic variants in the SMAD3 gene [PDF]

, 2018
Background: Predominant cardiovascular manifestations in the spectrum of Heritable Thoracic Aortic Disease include by default aortic root aneurysms- and dissections, which may be associated with aortic valve disease.
Aalberts, Alpendurada, Audenaert, Backer, Campens, Chen, Cook, Gott, Hoffmann, Kesler, Kiotsekoglou, Kiotsekoglou, Knosalla, Laar, Linde, Loeper, Murdoch, Pyeritz, Regalado, Rouf, Rybczynski, Schaeffer, Tae, Yetman   +23 more
core   +2 more sources

Yield of Whole Genome Sequencing for Pathogenic Single Nucleotide Variants in Congenital Heart Disease: A Systematic Review and Meta‐Analysis

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective This systematic review and meta‐analysis aimed to assess the diagnostic yield of pathogenic or likely pathogenic (P/LP) single nucleotide variants (SNVs) using whole genome sequencing (WGS) in congenital heart disease (CHD). Methods A systematic search of three databases (2000–2024) was conducted, and two reviewers independently ...
Hiba J. Mustafa, Parisa Najjariasl, Faezeh Aghajani, Enaja V. Sambatur, Andrew Rodenbarger, Stephanie Guseh, Amy E. Roberts, Alireza A. Shamshirsaz   +7 more
wiley   +1 more source

Giant aneurysm of the atrial septum associated with premature closure of foramen ovale [PDF]

, 2005
Premature closure or restriction of foramen ovale (PCFO) is a rare congenital anomaly that can lead to a wide spectrum of cardiac malformations. This spectrum of secondary malformations appears to depend on the gestational timing of closure of the ...
Constantinos Chrysostomou, Rita L Romaguera, Maria M Rodriguez, GS Dawes, RL Naeye, JG Wilson, E Pesonen, M Lev, S Bharati, TT Nowlen, V Chobot, PA Stewart, R De Groot, J Stanek, AP Vlahos   +14 more
core   +1 more source

Left Ventricular Pseudoaneurysm Perceived as a Left Lung Mass

Çukurova Üniversitesi Tıp Fakültesi Dergisi, 2013
Left ventricular pseudo-aneurysm is a rare complication of aneurysmectomy. We present a case of surgically-treated left ventricular pseudo-aneurysm which was diagnosed three years after coronary artery bypass grafting and left ventricular aneurysmectomy.
Ugur Gocen
doaj  

Healthcare professional’s guide to cardiopulmonary exercise testing [PDF]

, 2015
Cardiopulmonary exercise testing (CPEX) is a valuable clinical tool that has proven indications within the fields of cardiovascular, respiratory and pre-operative medical care.
Frenneaux, Michael P., Gollop, Nicholas D., Loudon, Brodie L., Parasuraman, Sathish, Schwarz, Konstantin   +4 more
core   +1 more source

Longest survivor of pulmonary atresia with ventricular septal defect without surgical intervention

ESC Heart Failure, Volume 12, Issue 2, Page 1499-1507, April 2025.
Sang Zhou, Yu Wu, Guoran Li, Yongwen Qin, Man Qi, Zhitao Jin   +5 more
wiley   +1 more source

Sex‐based differences in outcomes between male and female patients with bicuspid aortic stenosis following transcatheter aortic valve replacement: A meta‐analysis

Precision Medical Sciences, EarlyView.
Central illustration: Sex‐based differences in outcomes between male and female patients with bicuspid aortic stenosis following transcatheter aortic valve replacement. Abstract Bicuspid aortic valve (BAV) is a common congenital anomaly leading to early aortic stenosis.
Muhammad Huzaifa Ahmed Khan, Muneeb Khawar, Asad Ullah Farooq, Azooba Khalid, Syed Muhammad Ahsan, M. Hamza Naseer Awan, Muhammad Soban Nisar, Asim Elahi, Muhammad Aqib Faizan, Iqra Shahid, Abdullah Munir Ahmed, Faseeh Haider, Rejina Chhetri   +12 more
wiley   +1 more source

Prenatal diagnosis of left ventricular aneurysm

Indian Journal of Radiology and Imaging, 2009
Fetal cardiac anomalies involving the ventricular and atrial septa, outflow tracts, chambers, and valves are often encountered in routine screening. However, the prenatal detection of a fetal left ventricular aneurysm is rare.
K Balakumar
doaj   +1 more source

Ventricular‐Vascular Coupling in Marfan and Non‐Marfan Aortopathies [PDF]

, 2016
Background: Marfan syndrome (MFS) and familial non–syndromal thoracic aortic aneurysm and dissection (ns‐TAAD) are genetic aortopathies causing aortic dilatation with increased aortic stiffness.
Hambly, Brett, Jeremy, Richmond, Loeper, Farina, Lu, Yaxin, Oosterhof, Jantine, Robertson, Elizabeth, van den Dorpel, Mark, van der Linde, Denise   +7 more
core   +1 more source

Tissue‐retained needles in people who inject drugs: A systematic review of case reports and series on clinical presentations, complications and management

Addiction, EarlyView.
Abstract Background and aims Tissue‐retained needles from intravenous drug use can cause rare but severe complications, ranging from local to systemic infections to needle embolization. Due to the limited evidence and the lack of epidemiological studies on the issue, we systematically reviewed the literature focusing on case reports and case series on ...
Heidi Laukkala, Anna Nevalainen, Irina Rinta‐Kiikka, Samuel Heikkilä, Sisu Kiuru, Markku Sumanen, Otso Arponen, Olli Nevalainen   +7 more
wiley   +1 more source