Results 31 to 40 of about 30,274 (312)

Original Research. Diagnosis of the Aortic Coarctation in the Neonatal Period — a Critical Condition in the Emergency Room

Journal of Cardiovascular Emergencies, 2017
Background: Critical coarctation of the aorta is the most common congenital heart disease with ductal-dependent systemic circulation. In severe forms, this disease represents a critical condition, which can become life-threatening.
Rusu Simina-Elena, Toma Daniela, Blesneac Cristina, Matei Laura, Ghiragosian Claudiu, Togănel Rodica   +5 more
doaj   +1 more source

Endovascular Treatment of Coarctation of the Aorta with a Self-Expanding Endoprosthesis: How I Do It Using the Braile Dominus® Coarctation Aorta Device

Brazilian Journal of Cardiovascular Surgery, 2021
The coarctation of the aorta is a relatively highly prevalent congenital heart disease and may be diagnosed as an underline cause of hypertension in adolescents and adults.
Rodrigo Petersen Saadi, Eduardo Keller Saadi, Ana Paula Tagliari, Marina Petersen Saadi   +3 more
doaj   +1 more source

Aortic Coarctation: Recent Developments in Experimental and Computational Methods to Assess Treatments for this Simple Condition [PDF]

, 2010
Coarctation of the aorta (CoA) is often considered a relatively simple disease, but long-term outcomes suggest otherwise as life expectancies are decades less than in the average population and substantial morbidity often exists.
Feinstein, Jeffrey A., LaDisa, John F., Taylor, Charles A.   +2 more
core   +2 more sources

Iatrogenic coarctation caused by branched thoracic endovascular aortic repair treated with Palmaz XL stent and triple kissing balloon technique

Journal of Vascular Surgery Cases and Innovative Techniques, 2021
We have described a technique to treat iatrogenic coarctation caused by a branched thoracic endovascular aortic repair (TEVAR) procedure with a Palmaz XL stent (Palmaz Genesis; Cordis Corp, a Cardinal Health Company, Milpitas, Calif) and triple kissing ...
Wolf Eilenberg, MD, PhD, Giuseppe Panuccio, MD, PhD, Fiona Rohlffs, MD, PhD, Ahmed S. Eleshra, MD, PhD, Franziska Heidemann, MD, Tilo Kölbel, MD, PhD   +5 more
doaj   +1 more source

Different patterns of cerebral and muscular tissue oxygenation 10 years after coarctation repair [PDF]

, 2019
The purpose of this study was to assess whether the lower exercise tolerance in children after coarctation repair is associated with alterations in peripheral tissue oxygenation during exercise.
Boone, Jan, Bové, Thierry, Coomans, Ilse, De Groote, Katya, De Wilde, Hans, De Wolf, Daniël, François, Katrien, Moerman, Anneliese, PANZER, JOSEPH, Vandekerckhove, Kristof   +9 more
core   +2 more sources

3.3 ASSESSMENT OF AORTIC MORPHOLOGY IN A BICUSPID AORTIC VALVE POPULATION

Artery Research, 2017
Background: Bicuspid aortic valve (BAV) is a congenital heart disease associated with aortic wall abnormalities and co-existing with other congenital defects (e.g. aortic coarctation). This study aimed to explore aortic shape features in a BAV population,
Froso Sophocleous, Benedetta Biffi, Elena Giulia Milano, Cha Rajakaruna, Massimo Caputo, Costanza Emanueli, Chiara Bucciarelli-Ducci, Tom Gaunt, Silvia Schievano, Giovanni Biglino   +9 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

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

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