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pro vyhledávání: '"DCM, Dilated cardiomyopathy"'
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Publikováno v:
ESC Heart Failure, Vol 7, Iss 4, Pp 1909-1916 (2020)
Abstract Aims Hypokinetic non‐dilated cardiomyopathy (HNDC), which is determined by impaired left ventricular (LV) systolic function despite normal LV size, has been categorized as a subgroup of dilated cardiomyopathy (DCM) spectrum. Lack of data r
Externí odkaz:
https://doaj.org/article/c0c2c93bcc744569b113be1c02c05585
Publikováno v:
JACC: Basic to Translational Science
Highlights • Knowledge of the genetic etiologies of cardiomyopathies has created novel opportunities for treatments. • Emerging treatments targets include gene therapy, myofilament function, protein quality control, and metabolism. • Considerat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c656f79b564e9e437a00ca02b88041ed
https://doi.org/10.1016/j.jacbts.2021.07.012
https://doi.org/10.1016/j.jacbts.2021.07.012
Autor:
Birgitta K. Velthuis, Arco J. Teske, Dennis Bosboom, Reinder Evertz, Rob W Roudijk, Floris E A Udink Ten Cate, Carlo Marcelis, Anneline S.J.M. te Riele
Publikováno v:
JACC Case Reports
JACC: Case Reports, Vol 2, Iss 6, Pp 919-924 (2020)
JACC: Case Reports, Vol 2, Iss 6, Pp 919-924 (2020)
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is rarely diagnosed in childhood. We describe the case of a 9-year-old girl with genetically confirmed ARVC who presented with syncope, ventricular arrhythmia, and biventricular myocardial dysfun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4b93469ce060530dcfb6edccf2aec8f
https://doi.org/10.1016/j.jaccas.2020.01.006
https://doi.org/10.1016/j.jaccas.2020.01.006
Autor:
Felix Maverick R. Uy, Phong Teck Lee, Calvin W. L. Chin, Jie Sheng Foo, Thu-Thao Le, Ju Le Tan
Publikováno v:
JACC: Case Reports, Vol 2, Iss 5, Pp 740-744 (2020)
JACC Case Reports
JACC Case Reports
We report a case of coronary artery compression and athlete's heart in a patient with a history of transposition of the great arteries. We present the diagnostic dilemmas and demonstrate the use of cardiac magnetic resonance imaging and cycle-ergomet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e45b00ca88d9e2baf6be7f6ae8a945f9
http://www.sciencedirect.com/science/article/pii/S2666084920303326
http://www.sciencedirect.com/science/article/pii/S2666084920303326
Autor:
R. Mohan, T. Muralikrishna, R. Veena, K.G. Sureshrao, A. Ajay, K. Ramasubramanian, D. Jagdish, R. Ravikumar, K. Ganapathy Subramaniam, Komarakshi Balakrishnan
Publikováno v:
Indian Heart Journal, Vol 72, Iss 6, Pp 524-534 (2020)
Indian Heart Journal
Indian Heart Journal
Objective: End stage heart failure is a lethal disease with a dismal 5 year survival. Heart transplantation has proven to be a highly effective modality of treatment in appropriately selected group of such patients. This is a retrospective analysis o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee17d524c01008ad2fba862a47ee2b8b
http://www.sciencedirect.com/science/article/pii/S0019483220302339
http://www.sciencedirect.com/science/article/pii/S0019483220302339
Publikováno v:
JACC: CardioOncology
Background Adriamycin-associated cardiomyopathy (ACM) can lead to end-stage heart failure requiring advanced heart failure therapies. Objectives This study sought to provide post–cardiac transplant survival data in patients with ACM in the contempo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efbf64ec77f95b1a43cddbf5997391d1
https://pubmed.ncbi.nlm.nih.gov/34396337
https://pubmed.ncbi.nlm.nih.gov/34396337
Autor:
Clarissa P.C. Gomes, Yvan Devaux, Esther E. Creemers, Christoph Dieterich, Antonio Salgado-Somoza, Mitja Luštrek
Publikováno v:
Non-coding RNA Research
Non-coding RNA Research, Vol 3, Iss 1, Pp 1-11 (2018)
Non-coding RNA Research, Vol 3, Iss 1, Pp 1-11 (2018)
Until recently considered as rare, circular RNAs (circRNAs) are emerging as important regulators of gene expression. They are ubiquitously expressed and represent a novel branch of the family of non-coding RNAs. Recent investigations showed that circ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fa298b222fc7a3ee3c497231ebd3e36
https://doi.org/10.1016/j.ncrna.2018.02.002
https://doi.org/10.1016/j.ncrna.2018.02.002
Autor:
Linnea M, Baudhuin
Publikováno v:
Journal of the American College of Cardiology
Background Hypertrophic cardiomyopathy (HCM) is caused by rare variants in sarcomere-encoding genes, but little is known about the clinical significance of these variants in the general population. Objectives The goal of this study was to compare lif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::54b36173db722d4b3dfc87db31dce540
https://pubmed.ncbi.nlm.nih.gov/34503678
https://pubmed.ncbi.nlm.nih.gov/34503678
Autor:
Yukako Domoto, Yumiko Hosoya, Masamichi Ito, Toshiyuki Ko, Hiroyuki Morita, Yukari Uemura, Takashige Tobita, Shintaro Yamada, Masaru Hatano, Kanna Fujita, Issei Komuro, Seitaro Nomura, Eisuke Amiya, Masashi Fukayama, Manami Katoh, Masahiro Satoh, Hiroyuki Aburatani
Publikováno v:
JACC: Basic to Translational Science
JACC: Basic to Translational Science, Vol 4, Iss 6, Pp 670-680 (2019)
JACC: Basic to Translational Science, Vol 4, Iss 6, Pp 670-680 (2019)
Visual Abstract
Highlights • Patients with dilated cardiomyopathy who achieved LVRR have a favorable prognosis, but it is still difficult to precisely predict LVRR in the clinical setting. • Immunostaining of DNA damage markers such as PAR i
Highlights • Patients with dilated cardiomyopathy who achieved LVRR have a favorable prognosis, but it is still difficult to precisely predict LVRR in the clinical setting. • Immunostaining of DNA damage markers such as PAR i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::174547be6b56c9c36389f195a29ed5b0
http://europepmc.org/articles/PMC6834953
http://europepmc.org/articles/PMC6834953