Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Congenital cardiomyopathy"'
Autor:
T.O. Kryuchko, S.M. Tanianska
Publikováno v:
Zdorovʹe Rebenka, Vol 18, Iss 6, Pp 479-482 (2023)
Diseases of cardiovascular system in children present an extremely urgent problem nowadays. According to the latest epidemiological studies, there has been an increase by almost 3.2 % in congenital heart disease in Ukrainian children over the past 20
Externí odkaz:
https://doaj.org/article/9b72d25f58f0411ea260cb80aa1012f5
Autor:
Anissa Souidi, Krzysztof Jagla
Publikováno v:
Cells, Vol 10, Iss 11, p 3078 (2021)
The Drosophila heart, also referred to as the dorsal vessel, pumps the insect blood, the hemolymph. The bilateral heart primordia develop from the most dorsally located mesodermal cells, migrate coordinately, and fuse to form the cardiac tube. Though
Externí odkaz:
https://doaj.org/article/d35c9e9f2b5d45ba801f697b16baae6e
Akademický článek
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Autor:
Neiberg de Alcantara Lima, Mark Loehrke, Stela Maria Vitorino Sampaio, Antonio Thomaz de Andrade
Publikováno v:
Journal of Cardiac Arrhythmias. 33:188-192
Long QT syndrome is one of the most feared entities in hospitalized patients due to the potential risk for ventricular tachycardia and sudden death. Association between channelopathies and congenital cardiomyopathy is a new entity that has been studi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af18ab6e659f2bbc85ef5d2e70b1cb10
https://doi.org/10.24207/jca.v33i4.3426
https://doi.org/10.24207/jca.v33i4.3426
Akademický článek
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Autor:
Sankar Chandra Mandal, Sudeb Mukherjee
Publikováno v:
Journal of Cardiovascular Medicine and Cardiology. 7:122-124
The ventricular non-compaction or spongy myocardium is a rare congenital cardiomyopathy which is caused by defective morphogenesis of myocardium during embryonic life. It is characterised by excessive, coarse trabeculations within ventricular myocard
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5965456972e7096537e373463cf69cdf
https://doi.org/10.17352/2455-2976.000125
https://doi.org/10.17352/2455-2976.000125
Publikováno v:
Annales de Cardiologie et d'Angéiologie. 68:120-124
Isolated non-compaction of the left ventricle (NCVG) is a rare congenital cardiomyopathy resulting from the shutdown of normal embryogenesis of the myocardium. Its main feature is the existence of many deep heart-related ventricular trabeculations, g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d1160da674a4ae5bcf074bc8154aacc
https://doi.org/10.1016/j.ancard.2018.08.018
https://doi.org/10.1016/j.ancard.2018.08.018
Publikováno v:
Cirugía y Cirujanos. 85:539-543
ResumenAntecedentesEl miocardio no compactado del ventrículo izquierdo es una miocardiopatía congénita caracterizada por hipertrabeculación del VI y prominentes recesos intertrabeculares. La incidencia oscila entre 0.15% a 2.2%. Las manifestacion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::095f27e5698a11acdc07164e405919f9
https://doi.org/10.1016/j.circir.2016.09.001
https://doi.org/10.1016/j.circir.2016.09.001
Publikováno v:
Cureus
Ventricular noncompaction is a rare congenital cardiomyopathy resulting from failure in cardiac embryogenesis. Both left and right ventricular involvement has been reported in nature. We present a case of a 69-year-old male presenting with atrial fib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3971fcfde1afb6376c534048f4eedd86
http://europepmc.org/articles/PMC6538116
http://europepmc.org/articles/PMC6538116
Publikováno v:
Hellenic Journal of Cardiology, Vol 57, Iss 1, Pp 23-29 (2016)
Introduction Noncompaction cardiomyopathy (NCCM) is a rare congenital cardiomyopathy characterised by a distinctive 2-layered appearance of the myocardium due to hypertrabecularisation and deep intertrabecular recesses. The present study was designed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09d18af3b6d53bdaacf5af9f214155ea