Zobrazeno 1 - 10
of 36
pro vyhledávání: '"T. G. Vaikhanskaya"'
Publikováno v:
Евразийский Кардиологический Журнал, Vol 0, Iss 2, Pp 26-37 (2023)
Purpose. To study the diagnostic value of cascade family screening and the spectrum of genetic variants in patients with familial and sporadic DCM, assess clinical outcomes and comparative analysis of 5-year event-free survival.Materials and methods.
Externí odkaz:
https://doaj.org/article/f8d78ffeb2f8466faee925185dd3f873
Publikováno v:
Российский кардиологический журнал, Vol 28, Iss 11 (2023)
Aim. To study the epidemiological profile and long-term prognostic significance of atrial fibrillation (AF) as a risk factor for adverse clinical outcomes in patients with dilated cardiomyopathy (DCM).Material and methods. The study included 270 pati
Externí odkaz:
https://doaj.org/article/6ebb0507ae5d4625b856731b7614616f
Publikováno v:
Российский кардиологический журнал, Vol 26, Iss 10 (2021)
Aim. To study the diagnostic significance of genetic testing in patients with dilated cardiomyopathy (DCM), identify predictors of life-threatening ventricular tachyarrhythmias (VTAs) and assess adverse clinical outcomes in different genetic groups.M
Externí odkaz:
https://doaj.org/article/8d323a7b470b4ea9b93f60b735e50fcc
Autor:
T. G. Vaikhanskaya, T. M. Kaptsiukh, T. V. Kurushko, L. N. Sivitskaya, O. D. Liaudanski, N. G. Danilenko
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 100-109 (2019)
The article provides a brief overview of the problems of diagnostics and etiological verification of restrictive cardiomyopathy (RCMP). Multiple causes lead to the restrictive phenotype of intracardiac hemodynamics and diastolic dysfunction of the he
Externí odkaz:
https://doaj.org/article/2714e9b3b28c497c916f7f7217052be6
Autor:
T. G. Vaikhanskaya, L. N. Sivitskaya, T. V. Kurushko, T. V. Rusak, O. D. Levdansky, N. G. Danilenko, O. G. Davydenko
Publikováno v:
Российский кардиологический журнал, Vol 25, Iss 11 (2020)
Non-compaction cardiomyopathy (NCM) is a rare heart disease characterized by a two-layered ventricular wall, comprising a thinner compact epicardial layer and an inner non-compacted layer. However, only structural and morphological data without a tho
Externí odkaz:
https://doaj.org/article/2d1f43babb3c42b6b9399bc9aa292324
Publikováno v:
Российский кардиологический журнал, Vol 25, Iss 11 (2020)
Atrial cardiomyopathy (ACM) is a relatively common but clinically underestimated disorder, which is characterized by an increased atrial size and dysfunction. Previously, ACM was considered a primary disorder, but in 2016 this concept was revised by
Externí odkaz:
https://doaj.org/article/a64e2f9f3c834719a3c573003c0034b1
Autor:
T. G. Vaikhanskaya, L. N. Sivitskaya, T. V. Kurushko, T. V. Rusak, O. D. Levdansky, N. G. Danilenko, O. G. Davydenko
Publikováno v:
Российский кардиологический журнал, Vol 25, Iss 12 (2020)
Improvement of high-tech methods of cardiac imaging and new generation sequencing with their introduction into widespread practice has significantly expanded the potential of diagnosis of rare cardiomyopathies. Modern imaging methods make it easy to
Externí odkaz:
https://doaj.org/article/31910bd825224d80805afaa050cbf8f9
Autor:
T. G. Vaikhanskaya, L. N. Sivitskaya, T. V. Kurushko, T. V. Rusak, O. D. Levdansky, N. G. Danilenko, O. G. Davydenko
Publikováno v:
Российский кардиологический журнал, Vol 25, Iss 10 (2020)
Recent multicenter studies using high-tech cardiac imaging and novel translational technologies have shown that cardiac fibrofatty replacement, characteristic of arrhythmogenic cardiomyopathy (ACM), is observed in both ventricles; left ventricular (L
Externí odkaz:
https://doaj.org/article/9e1bfc0d43b74db29da18801cc7784b2
Autor:
T. G. Vaikhanskaya, L. N. Sivitskaya, T. V. Kurushko, D. P. Ermakovich, E. V. Zasim, N. G. Danilenko
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 151-158 (2018)
Mutations in the genes encoding desmosomal proteins cause a wide range of diseases associated with abnormalities of the skin, hair and heart. In 45-50% these mutations determine the development of arrhythmogenic right ventricular cardiomyopathy. Toda
Externí odkaz:
https://doaj.org/article/a56ebc7f397c499c93d8c22341a2c8a6
Publikováno v:
Евразийский Кардиологический Журнал, Vol 0, Iss 1, Pp 3-11 (2016)
This article presents the current view on the structure and functions of nuclear lamin proteins, pathological phenotypes of persons with LMNA mutations and clinical problems of lamin-related dilated cardiomyopathy diagnostics and management. Dilated
Externí odkaz:
https://doaj.org/article/6921482a975c4b1f93220f85685384ac