Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Yu. A. Lutokhina"'
Autor:
Yu. A. Lutokhina, T. B. Andrushchishina, T. N. Erdniev, G. A. Mekhtieva, I. L. Petushkov, A. S. Yasneva, O. V. Blagova
Publikováno v:
Кардиоваскулярная терапия и профилактика, Vol 23, Iss 8 (2024)
Fever of unknown origin (FUO), despite the wide diagnostic potential of modern medicine, remains a difficult problem for clinicians. Often, making a correct diagnosis requires a comprehensive examination of the patient, as well as the joint work of d
Externí odkaz:
https://doaj.org/article/85eb611cdf3941f0bd1e927616320da7
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, D. Kh. Ainetdinova, E. A. Kogan, Yu. A. Lutokhina, V. M. Novosadov, P. O. Savina, A. Yu. Zaitsev, A. D. Kukleva, S. E. Rubtsova, S. N. Krivtsova, A. V. Nedostup
Publikováno v:
Российский кардиологический журнал, Vol 27, Iss 9 (2022)
The possibility of heart inflammation (both myocardial and endocardial) months after a coronavirus disease 2019 (COVID-19) has not been practically studied, especially since approaches to the treatment of myocarditis in combination with various endoc
Externí odkaz:
https://doaj.org/article/e07449b8c45145d6b2f1ec5fd422fa11
Autor:
D. V. Ruchkin, A. A. Nartova, A. I. Zaitseva, Yu. A. Lutokhina, O. V. Blagova, I. N. Alijeva, N. D. Sarkisova, A. V. Nedostup
Publikováno v:
Кардиоваскулярная терапия и профилактика, Vol 21, Iss 7 (2022)
Aim. To establish the prevalence of myocarditis and primary (genetic) cardiomyopathies (CMP) among patients in a cardiology hospital.Material and methods. Medical records of 671 patients of the cardiology department were analyzed. The diagnosis at ad
Externí odkaz:
https://doaj.org/article/db75dac8bb0a4fde8768447b75ef7879
Autor:
O. V. Blagova, Yu. A. Lutokhina, D. H. Ainetdinova, V. P. Sedov, A. N. Volovchenko, D. A. Parfenov, N. P. Mozheiko
Publikováno v:
Vestnik Transplantologii i Iskusstvennyh Organov, Vol 22, Iss 4, Pp 173-182 (2021)
Myocarditis has polymorphic clinical manifestations and is one of the main causes of heart transplantation. We present a clinical case of a 43-year-old female patient who was admitted to the clinic with biventricular heart failure (NYHA class 3–4).
Externí odkaz:
https://doaj.org/article/722b93a2258144faa541cb3e2d4f452a
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
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
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