Results 61 to 70 of about 54,421 (175)

Simultaneous Volumetric T1 and T2 Mapping With Blood‐ and Fat‐Suppression in Abdominal Aortic Aneurysms

Magnetic Resonance in Medicine, EarlyView.
ABSTRACT Purpose To develop and validate a protocol for simultaneous volumetric T1 and T2 mapping with blood‐ and fat‐suppression, and apply it to patients with abdominal aortic aneurysms (AAA) to assess tissue characteristics. Methods A spoiled gradient echo (SPGR) variable flip angle (VFA) acquisition was modified with preparation modules to suppress
Wilhelm Stehling, Myrte Wennen, Eva Aalbregt, Eric Schrauben, Pim van Ooij, Kak Khee Yeung, Aart J. Nederveen, Oliver J. Gurney‐Champion   +7 more
wiley   +1 more source

Transposition of an anomalous left vertebral artery followed by endovascular treatment of descending thoracic aortic aneurysm using a branched endoprosthesis

Annals of Vascular Surgery - Brief Reports and Innovations
The anomalous origin of the left vertebral artery from the aorta is the second most common anatomical alteration of the aortic arch. We present a case of a patient with a descending thoracic aortic aneurysm and an anomalous origin of a dominant left ...
Rogério do Lago Franco, Ualid Saleh Hatoum, Johann Viktor Müller, Miyoko Massago, Luciano de Andrade   +4 more
doaj   +1 more source

Spontaneous subarachnoid haemorrhage due to coarctation of aorta and intraspinal collaterals : a rare presentation [PDF]

, 2012
The occurrence of spontaneous subarachnoid haemorrhage (SAH) in association with coarctation of thoracic aorta and absence of intracranial aneurysm is a rare association.
Devara, Anil K.V., Joseph, S., Uppu, S.C.   +2 more
core  

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

Successful open surgical treatment for persistent type II endoleak following thoracic endovascular aortic repair: a case report

Journal of Cardiothoracic Surgery
Background The occurrence of type II endoleaks after endovascular repair of aortic aneurysm has gradually gained increasing attention. We present a case of a patient with an expanding aneurysm after thoracic endovascular aortic repair (TEVAR) for a type ...
June Lee, Do Yeon Kim, Hyun Ah Lim, Seok Beom Hong, Yong Han Kim, Hwan Wook Kim   +5 more
doaj   +1 more source

Hypertrophic Cardiomyopathy as a Key Feature of MRAS‐Related Noonan Syndrome: New Case and Comprehensive Literature Review

Prenatal Diagnosis, EarlyView.
ABSTRACT Noonan syndrome (NS) is a rare multisystemic condition among the RASopathy group, characterized by a broad phenotypic spectrum and genetic variability. It results from pathogenic variants in genes regulating the RAS/MAPK pathway, affecting cell proliferation and differentiation.
Romain Martineau, Constance Wells, Florent Fuchs, Sophie Collardeau‐Frachon, Valentin Ruault, Sophie Colomb, Jean‐Michel Faure, Caroline Bartholmot, Marie Vincenti, Benjamin Ganne, Marjolaine Willems   +10 more
wiley   +1 more source

Inhibition of MAPK-Erk pathway in vivo attenuates aortic valve disease processes in Emilin1-deficient mouse model [PDF]

, 2017
Aortic valve disease (AVD) is a common condition with a progressive natural history, and presently, there are no pharmacologic treatment strategies. Elastic fiber fragmentation (EFF) is a hallmark of AVD, and increasing evidence implicates developmental ...
Aikawa, Barnette, Basalyga, Bonow, Brown-Augsburger, Brunskill, Brunskill, Chung, Fondard, Franco, Gallegos, Gapski, Ghosh, Gu, Helske, Hinton, Hinton, Holm, Ihn, Iverson, Jensen, Keane, Krenz, Liang, Lindeman, Marshall, Mercer, Mohler, Mozaffarian, Munjal, Nishimura, Nkomo, Perrotta, Poggio, Potter, Rajamannan, Rossebo, Sauls, Schmieder, Schoen, Starcher, Vesely, Wirrig, Wylie-Sears, Xiong, Xiong   +45 more
core   +2 more sources

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

Endovascular management of a rare complication of an aortic coarctation

Radiology Case Reports, 2018
A 28-year-old pregnant woman presents with arterial hypertension of the upper limbs. The examination suggests an aortic coarctation. After a normal delivery, a contrast-enhanced computed tomography revealed a subocclusive aortic coarctation of the ...
Ahoury N'guessan Judicael, MD, Michael Vouche, MD, David Denaeghel, MD, Salvatore Murgo, MD, José Ferreira, PhD   +4 more
doaj   +1 more source