Results 31 to 40 of about 26,235 (263)

Mixed Valvular Disease Following Transcatheter Aortic Valve Replacement: Quantification and Systematic Differentiation Using Clinical Measurements and Image-Based Patient‐Specific In Silico Modeling [PDF]

, 2020
Background: Mixed valvular disease (MVD), mitral regurgitation (MR) from pre‐existing disease in conjunction with paravalvular leak (PVL) following transcatheter aortic valve replacement (TAVR), is one of the most important stimuli for left ventricle (LV)
Amrute, Junedh M., Ben-Assa, Eyal, Blanke, Philipp, Brown, Jonathan, de la Torre Hernandez, Jose M., Edelman, Elazer R., Garcia Camarero, Tamara, Keshavarz-Motamed, Zahra, Khodaei, Seyedvahid, Lee, Suk Joon, Leipsic, Jonathon, Rikhtegar Nezami, Farhad, Ruano Calvo, Javier, Sellers, Stephanie   +13 more
core   +1 more source

MODERN VIEWS ON THE GENE NOTCH1 MUTATIONS ROLE FOR AORTIC COARCTATION

Российский кардиологический журнал, 2014
Aim. By the observation of aortic coarctation victims families, to reveal factors predisposing to the disease development, and to evaluate the prevalence of NOTCH1 genes mutation/replacements in patients with this kind of defect.
T. N. Tatarinova, O. A. Freilichman, A. A. Kostareva, E. V. Grekhov, O. M. Moiseeva   +4 more
doaj   +1 more source

Turner syndrome and associated problems in turkish children: A multicenter study [PDF]

, 2015
Objective: Turner syndrome (TS) is a chromosomal disorder caused by complete or partial X chromosome monosomy that manifests various clinical features depending on the karyotype and on the genetic background of affected girls.
Abacı, A., Abalı, S., Adal, E., Akın, L., Akıncı, A., Akyürek, N., Andıran, N., Anık, A., Atabek, M.E., Ataş, A., Aydın, B.K., Açıkel, C., Baş, F., Baş, S., Baş, V.N., Bereket, A., Binay, Ç., Bolu, S., Bondy, C., Bulan, K., Büyükinan, M., Can, H.D., Cinaz, P., Darcan, Ş., Darendeliler, F., Demir, K., Demirbilek, H., Demirel, F., Doğan, D., Doğan, M., Döneray, H., Dündar, B., Eklioğlu, B.S., Emeksiz, H.C., Ercan, O., Eren, E., Ersoy, B., Evliyaoğlu, O., Fidancı, K., Gökşen, D., Gül, D., Gürbüz, F., Hatun, Ş., Kaba, S., Kara, C., Karagüzel, G., Keskin, M., Kızılay, D., Orbak, Z., Pirgon, Ö., Polat, A., Poyrazoğlu, Ş., Sarı, E., Sağlam, H., Tarım, Ö., Tepe, D., Topaloğlu, A.K., Turan, S., Yeşilkaya, E., Yüksel, B., Çakır, E.D., Çatlı, G., Çelik, N., Çizmecioğlu, F., Ökten, A., Önal, H., Özbek, M.N., Özen, S., Özgen, T., Özhan, Bayram, Özkan, B., Ünüvar, T., Şen, Y., Şimşek, E.   +73 more
core   +1 more source

Simultaneous correction of aortic coarctation and bicuspid aortic valve in an adult patient (case report)

Український журнал серцево-судинної хірургії, 2019
Aortic coarctation is one of the most frequent congenital heart defects; the frequency is in the range of 6-7%. Aortic coarctation is often associated with other heart defects, namely: a bicuspid aortic valve, an interventricular septal defect, and ...
S. V. Varbanets, A. Y. Pukas, M. M. Furman   +2 more
doaj   +1 more source

Two stage hybrid approach for complex aortic coarctation repair

Journal of Cardiothoracic Surgery, 2009
Background Management of an adult patient with aortic coarctation and an associated cardiac pathology poses a great surgical challenge since there are no standard guidelines for the therapy of such complex pathology.
Crockett James, Tsaousis George, Panagopoulos Nikolaos, Ekonomidis Stella, Koletsis Efstratios, Panagiotou Matthew   +5 more
doaj   +1 more source

Including Aortic Valve Morphology in Computational Fluid Dynamics Simulations: Initial Findings and Application to Aortic Coarctation [PDF]

, 2012
Computational fluid dynamics (CFD) simulations quantifying thoracic aortic flow patterns have not included disturbances from the aortic valve (AoV). 80% of patients with aortic coarctation (CoA) have a bicuspid aortic valve (BAV) which may cause adverse ...
Cava, Joseph Richard, Ellwein, Laura M, Gandy, Kimberly L., Krolikowski, Mary M., LaDisa, John F., Pelech, Andrew N., Samyn, Margaret M., Shadden, Shawn C., Wendell, David C.   +8 more
core   +2 more sources

Acute anterior wall myocardial infraction in asymptomatic severe aortic Coarctation in young adult – A rare case

Indian Heart Journal, 2016
Coarctation of Aorta is not rare in general population. Aortic Coarctation represents about 5–8% of all congenital cardiac diseases, and it is commonly associated with bicuspid aortic valve.
Gaurav Singhal, Vijay Pathak
doaj   +1 more source

Incidental finding of undiagnosed aortic coarctation in an elderly patient with a rare association with thymic carcinoma: a case report with review of the literature

Radiology Case Reports, 2023
Aortic coarctation is a congenital malformation that is relatively prevalent, occurring in approximately 5 out of every 1000 births. The narrowing typically happens at the aortic isthmus between the left subclavian artery and the arterial ligament. It is
Manar Ezzahi, MD, Ayman Bijbij, MD, Amal Akammar, MD, Nizar El Bouardi, MD, Meriem Haloua, MD, Moulay Youssef Alaoui Lamrani, MD, Meryem Boubbou, MD, Mustapha Maaroufi, MD, Badreeddine Alami, MD   +8 more
doaj   +1 more source

Aortic coarctation in an asymptomatic patient with arterial hypertension initially evaluated by Doppler ultrasound in the emergency room: A case report

Radiology Case Reports, 2022
Aortic coarctation is a severe pathology that can be underdiagnosed in pediatric patients. We present 1 case of a patient diagnosed with aortic coarctation in the emergency department, referred by his treating physician when detecting high blood pressure
César Hayashi Mercado, MD, Abelardo Alexander Aguilar West, MD, Reynaldo Ramírez Chacón, MD   +2 more
doaj   +1 more source

Aortic valve and aortic arch pathology after coarctation repair [PDF]

, 2003
OBJECTIVE: To investigate the incidence of clinical problems related to a bicuspid valve (aortic stenosis and regurgitation) and the incidence of ascending aorta and aortic arch pathology in combination with coarctation repair.
Boersma, H. (Eric), Bogers, A.J.J.C. (Ad), Heijdra, R.J., Meijboom, F.J. (Folkert), Roos-Hesselink, J.W. (Jolien), Scholzel, B.E., Simoons, M.L. (Maarten), Spitaels, S.E.C. (Silja)   +7 more
core   +1 more source