Zobrazeno 1 - 10
of 359
pro vyhledávání: '"Dilated cardiomyopathy (DCM)"'
Autor:
Irene Picciolli, Angelo Ratti, Berardo Rinaldi, Anwar Baban, Maria Iascone, Gaia Francescato, Alessia Cappelleri, Monia Magliozzi, Antonio Novelli, Giovanni Parlapiano, Anna Maria Colli, Nicola Persico, Stefano Carugo, Fabio Mosca, Maria Francesca Bedeschi
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-8 (2024)
Abstract Background Dilated cardiomyopathy (DCM) is an etiologically heterogeneous group of diseases of the myocardium. With the rapid evolution in laboratory investigations, genetic background is increasingly determined including many genes with var
Externí odkaz:
https://doaj.org/article/e078afc74be34a5996afaeb4f2b7bb6a
Autor:
Teleah G. Belkin, Emma I. Masterman, Gunes S. Yildiz, Helen Kiriazis, Natalie A. Mellett, Jonathon Cross, Kyah Grigolon, Akshima Dogra, Daniel Donner, Roger Chooi, Amy Liang, Andrew R. Kompa, Junichi Sadoshima, Amanda J. Edgley, David W. Greening, Peter J. Meikle, Yow Keat Tham, Julie R. McMullen
Publikováno v:
Journal of Molecular and Cellular Cardiology Plus, Vol 11, Iss , Pp 100273- (2025)
We previously reported that plasmalogens, a class of phospholipids, were decreased in a setting of dilated cardiomyopathy (DCM). Plasmalogen levels can be modulated via a dietary supplement called alkylglycerols (AG) which has demonstrated benefits i
Externí odkaz:
https://doaj.org/article/909d78382e0e400787bfb45011da8c59
Autor:
SiYang Xue, HongJu Jiang
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
BackgroundObservational clinical studies suggest an association between dilated cardiomyopathy (DCM) and various factors including titin, cardiac troponin I (CTnI), desmocollin-2, the perinatal period, alcoholism, Behçet's disease, systemic lupus er
Externí odkaz:
https://doaj.org/article/486d2f843e884cb69286cb0ce701889a
Autor:
Dac Dai Tran, Nguyen Thi Kim Lien, Nguyen Van Tung, Nguyen Cong Huu, Phan Thao Nguyen, Do Anh Tien, Doan Thi Hoai Thu, Bui Quang Huy, Tran Thi Kim Oanh, Nguyen Thi Phuong Lien, Nguyen Thanh Hien, Nguyen Ngoc Lan, Le Tat Thanh, Nguyen Minh Duc, Nguyen Huy Hoang
Publikováno v:
Diagnostics, Vol 14, Iss 23, p 2709 (2024)
Background: Cardiomyopathy, including dilated cardiomyopathy (DCM) and hypertrophic cardiomyopathy (HCM), is a major cause of heart failure (HF) and a leading indication for heart transplantation. Of these patients, 20–50% have a genetic cause, so
Externí odkaz:
https://doaj.org/article/427c9547ae604f9b807957e899176bfb
Publikováno v:
Frontiers in Physiology, Vol 15 (2024)
The giant protein titin is an essential component of muscle sarcomeres. A single titin molecule spans half a sarcomere and mediates diverse functions along its length by virtue of its unique domains. The A-band of titin functions as a molecular bluep
Externí odkaz:
https://doaj.org/article/466e9e387fa344bab7c6ed4af6bf26b9
Autor:
Xuebin Ling, Yanjun Hou, Xingyu Jia, Youling Lan, Xiaoping Wu, Julan Wu, Wei Jie, Hui Liu, Shan Huang, Zhenling Wan, Tianfa Li, Junli Guo, Tiebiao Liang
Publikováno v:
Frontiers in Genetics, Vol 14 (2024)
Introduction:LMNA splicing mutations occur in 9.1% of cases with cardiac involvement cases, but the phenotype and severity of disease they cause have not yet been systematically studied. The aim of this study was to understand the clinical and pathog
Externí odkaz:
https://doaj.org/article/af6448337af747828ad84b0a54664efb
Autor:
Helen Triantafyllidi, Dionyssia Birmpa, Ignatios Ikonomidis, Dimitrios Benas, George Makavos, Dennis V. Cokkinos, Filippos Triposkiadis, Efstathios K. Iliodromitis
Publikováno v:
Hellenic Journal of Cardiology, Vol 70, Iss , Pp 28-35 (2023)
Objective: Little is known about the exercise-induced changes in the multidimensional mechanical properties of the heart. We aimed to evaluate the myocardial deformation indices (MDI) at rest and their response at peak exercise during the same cardio
Externí odkaz:
https://doaj.org/article/51f1c48209df4938bf0b4499d18ebb53
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
With the advent of next-generation whole genome sequencing, many variants of uncertain significance (VUS) have been identified in individuals suffering from inheritable hypertrophic cardiomyopathy (HCM). Unfortunately, this classification of a geneti
Externí odkaz:
https://doaj.org/article/c87043c9a16545e6aa5be99cbc31d3be
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.