Zobrazeno 1 - 10
of 63
pro vyhledávání: '"E. V. Zaklyazminskaya"'
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 19, Iss 2, Pp 179-185 (2023)
A 64-year-old female with a family history of hereditary hemorrhagic telangiectasia (HHT) was hospitalized due to complaints of dyspnea during light physical exertion and leg edema. HHT was diagnosed at 20 y.o., recurrent nasal bleeding started at ag
Externí odkaz:
https://doaj.org/article/0d4b23c48c334811a007ab23a435eedd
Autor:
Yu. A. Lutokhina, O. V. Blagova, E. A. Kogan, A. A. Nartov, V. R. Nartova, E. V. Zaklyazminskaya, S. L. Dzemeshkevich
Publikováno v:
Российский кардиологический журнал, Vol 28, Iss 11 (2023)
Aim. To assess the incidence of myocarditis in patients with primary myocardial hypertrophy and to study its contribution to the disease course.Material and methods. The study included 100 patients with primary left ventricular myocardial hypertrophy
Externí odkaz:
https://doaj.org/article/b7143c25195148e299d9aa73efece401
Autor:
O. V. Blagova, E. V. Pavlenko, N. V. Varionchik, V. P. Sedov, N. V. Gagarina, E. A. Mershina, M. E. Polyak, E. V. Zaklyazminskaya, A. V. Nedostup
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 18, Iss 1, Pp 27-35 (2022)
Aim. To study the place of NCM in the structure of DCM, its clinical features and influence on prognosis in comparison with other forms of DCM syndrome.Methods. The NCM registry includes 125 patients, mean age 46.4±15.1 years, 74 men and 51 women, m
Externí odkaz:
https://doaj.org/article/fa8149e033874d1eb376784f7edbbc68
Autor:
O. V. Blagova, E. A. Kogan, V. P. Sedov, Yu. A. Lutokhina, A. V. Nedostup, A. V. Ott, L. M. Dashinemaeva, E. V. Zaklyazminskaya
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 16, Iss 2, Pp 231-239 (2020)
Aim. To analyze the difficulties of diagnosis and the clinical features of the Danon disease in women.Results. An observation of Danon disease in a woman aged 18 years with an uncomplicated family history is presented. The early development of atrial
Externí odkaz:
https://doaj.org/article/40dbd18e60af42e9a7d276c707b0a460
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 47, Iss 7, Pp 603-613 (2019)
Cardiomyopathy (CMP) is a common group of cardiovascular disorders. Genetic (primary) cardiomyopathies are related to abnormalities in more than 100 genes, including the DES gene encoding desmin protein. Desmin is an essential member of the intermedi
Externí odkaz:
https://doaj.org/article/373582607bc54bcc8db7f819d665fec3
Autor:
Yu. A. Lutokhina, O. B. Blagova, A. G. Shestak, E. V. Zaklyazminskaya, S. A. Alexandrova, A. V. Nedostup
Publikováno v:
Российский кардиологический журнал, Vol 26, Iss 11 (2021)
This article describes evolution of criteria for arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C). The novel diagnostic criteria for ARVD/C published in 2020 are analyzed in detail, among which biventricular and leftdominant arrhyth
Externí odkaz:
https://doaj.org/article/653fe1971f2643eea4764342790bdce9
Autor:
N. N. Chakova, S. M. Komissarova, E. A. Zasim, T. V. Dolmatovich, E. S. Rebeko, S. S. Niyazova, E. V. Zaklyazminskaya, L. I. Plashchinskaya, M. V. Dudko
Publikováno v:
Российский кардиологический журнал, Vol 26, Iss 10 (2021)
Aim. To determine the spectrum of mutations in the genes responsible for the long QT syndrome (LQTS) and study their phenotypic manifestations in patients with LQTS in different age groups.Materials and methods. The study included 35 unrelated proban
Externí odkaz:
https://doaj.org/article/08e052b84a794d2093f9296e42b2ee93
Publikováno v:
Российский кардиологический журнал, Vol 26, Iss 10 (2021)
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a hereditary myocardial disease with a high risk of sudden cardiac death. The most common genetic forms of the disease are associated with desmosomal gene mutations.Aim. To study the prevalenc
Externí odkaz:
https://doaj.org/article/0a97366e9592472e954a023dbb13cca6
Autor:
Yu. A. Lutokhina, O. V. Blagova, A. V. Nedostup, S. A. Alexandrova, E. V. Evseeva, A. G Shestak, E. V. Zaklyazminskaya
Publikováno v:
Кардиоваскулярная терапия и профилактика, Vol 20, Iss 5 (2021)
Aim. To assess the contribution of genetic and inflammatory factors to the development of arrhythmogenic right ventricular cardiomyopathy (ARVC).Material and methods. The study involved 54 patients with ARVC (age, 38,7±14,1 years; men, 42,6%; mean f
Externí odkaz:
https://doaj.org/article/00331668a1854c5cbbc5befad908a933
Ventricular arrhythmias. Ventricular tachycardias and sudden cardiac death. 2020 Clinical guidelines
Autor:
D. S. Lebedev, E. N. Mikhailov, N. M. Neminuschiy, E. Z. Golukhova, V. E. Babokin, V. V. Bereznitskaya, E. S. Vasichkina, S. V. Garkina, S. P. Golitsyn, K. V. Davtyan, D. V. Duplyakov, E. V. Zaklyazminskaya, S. A. Zenin, E. A. Ivanitsky, R. A-G. Ildarova, V. N. Komolyatova, A. A. Kostareva, E. A. Kuchinskaya, L. Yu. Lajovich (Nesterenko), V. K. Lebedeva, T. A. Lyubimtseva, L. M. Makarov, S. E. Mamchur, M. M. Medvedev, N. Yu. Mironov, L. B. Mitrofanova, S. V. Popov, A. Sh. Revishvili, F. G. Rzayev, A. B. Romanov, R. B. Tatarsky, S. A. Termosesov, M. D. Utsumueva, M. S. Kharlap, D. A. Tsaregorodtsev, M. A. Shkolnikova, N. B. Shlevkov, E. V. Shlyakhto, Yu. V. Shubik, S. M. Yashin
Publikováno v:
Российский кардиологический журнал, Vol 26, Iss 7 (2021)
Russian Society of Cardiology (RSC).With the participation of Russian Scientific Society of Clinical Electrophysiology, Arrhythmology and Cardiac Pacing, Russian Association of Pediatric Cardiologists, Society for Holter Monitoring and Noninvasive El
Externí odkaz:
https://doaj.org/article/7431fbdba5a4472bbfc0d3f4f39ea29f