Zobrazeno 1 - 10
of 45
pro vyhledávání: '"A. Ya. Gudkova"'
Publikováno v:
Учёные записки Санкт-Петербургского государственного медицинского университета им. Акад. И.П. Павлова, Vol 30, Iss 1, Pp 50-61 (2023)
The objective was to study the clinical features of symptomatic hypertrophic cardiomyopathy (HCM) depending on the form (familial / non-familial), the age of onset and the presence of arterial hypertension (AH).Methods and materials. During 6 years,
Externí odkaz:
https://doaj.org/article/7c85a3b64b134cf099c095dcdf01b7ce
Autor:
V. G. Davydova, Е. I. Baranova, T. G. Bezhanishvili, A. N. Krutikov, A. A. Poliakova, S. A. Pyko, A. Ya. Gudkova
Publikováno v:
Учёные записки Санкт-Петербургского государственного медицинского университета им. Акад. И.П. Павлова, Vol 29, Iss 4, Pp 50-59 (2023)
The objective was to study the clinical features of symptomatic hypertrophic cardiomyopathy (HCM) depending on the age of onset and the presence of cardiometabolic risk factors.Methods and materials. From 2014 to 2020, 250 patients were examined, 100
Externí odkaz:
https://doaj.org/article/b7d44b2e69224c4685046e9c8511c482
Publikováno v:
Учёные записки Санкт-Петербургского государственного медицинского университета им. Акад. И.П. Павлова, Vol 28, Iss 2, Pp 23-32 (2021)
The objective of this study was to determine the association of polymorphic variants rs2305619 and rs3816527 of the PTX3 gene with clinical profile and outcomes in hypertrophic cardiomyopathy (HCM) patients.Methods and materials. The study population
Externí odkaz:
https://doaj.org/article/39030d695c3f454ca38f9dadb88990c5
Autor:
A. A. Streltsova, A. Ya. Gudkova
Publikováno v:
Учёные записки Санкт-Петербургского государственного медицинского университета им. Акад. И.П. Павлова, Vol 28, Iss 1, Pp 17-22 (2021)
This review presents the last literature data, concerning prevalence, clinical profile, diagnostic and treatment of apical hypertrophic cardiomyopathy (HCM), as less known among «classical» variants of HCM. It is also discussed the rare form of api
Externí odkaz:
https://doaj.org/article/bf3870bb6c4d47f19b6e4564c3f41ee4
Publikováno v:
Терапевтический архив, Vol 92, Iss 4, Pp 51-56 (2020)
Aim. To study the levels of circulating microRNA-21 in patients with hypertrophic cardiomyopathy (HCM) of different ages. Materials and methods. The study included 49 patients with HCM. The proportion of females was 55.1%, males 44.9%. The average
Externí odkaz:
https://doaj.org/article/e141ea3ba42248a3b7b07233d5c5c5b5
Autor:
S. A. Gabrusenko, A. Ya. Gudkova, N. A. Koziolova, S. A. Alexandrova, M. I. Berseneva, M. L. Gordeev, S. L. Dzemeshkevich, E. V. Zaklyazminskaya, O. B. Irtyuga, V. Yu. Kaplunova, A. A. Kostareva, A. N. Krutikov, D. A. Malenkov, T. N. Novikova, M. A. Saidova, M. K. Sanakoev, O. V. Stukalova
Publikováno v:
Российский кардиологический журнал, Vol 26, Iss 5 (2021)
Russian Society of Cardiology (RSC)With the participation: Russian Association of Cardiovascular SurgeonsEndorsed by: Research and Practical Council of the Ministry of Health of the Russian Federation Task Force: Gabrusenko S.A. (Chairman), Gudkova A
Externí odkaz:
https://doaj.org/article/7cbec82cfe3243a5a86da2d0003caf57
Autor:
O. V. Melnik, A. B. Malashicheva, Yu. V. Fomicheva, A. A. Khudyakov, A. Ya. Gudkova, D. I. Rudenko, M. A. Simonenko, Е. N. Mikhailov, D. S. Lebedev, E. S. Vasichkina, T. M. Pervunina, A. A. Kostareva
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 72-77 (2019)
Mutations in the LMNA gene cause developing of several phenotypes, both with isolated involvement of cardiac, muscle, adipose and bone tissues, and with their combination. The dominance of cardiovascular signs in the clinical performance and false cl
Externí odkaz:
https://doaj.org/article/36befde99f054c6d88dfee7d1ca3a85b
Autor:
T. G. Bezhanishvili, A. Ya. Gudkova, V. G. Davydova, S. E. Andreeva, A. N. Krutikov, E. N. Semernin, B. N. Kudryavtsev, S. A. Pyko, A. A. Kostareva, E. N. Shlyakhto
Publikováno v:
Российский кардиологический журнал, Vol 25, Iss 10 (2020)
Aim. To analyze associations of interleukin-6 receptor gene (IL6R) polymorphism (rs2228145) with the clinical course characteristics of hypertrophic cardiomyopathy (HCM) in groups of patients with various cardiometabolic risk factorsMaterial and meth
Externí odkaz:
https://doaj.org/article/4b1092a937204f80ae025eec673c9659
Autor:
I. V. Shlyk, A. A. Streltsova, V. M. Teplov, E. G. Gavrilova, A. N. Kulikov, A. N. Krutikov, M. G. Rybakova, I. A. Kuznetsova, S. E. Andreeva, T. G. Bezhanishvili, A. A. Khudiakov, A. A. Kostareva, A. Ya. Gudkova
Publikováno v:
Российский кардиологический журнал, Vol 25, Iss 10 (2020)
We report a case of mixed phenotype cardiomyopathy (non-compaction cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy), associated with DSP genetic variant. The sudden cardiac death was the first and only symptom.
Externí odkaz:
https://doaj.org/article/ffbcead0b10645e3be86775627843647
Autor:
O. V. Melnik, T. S. Loevets, T. L. Vershinina, A. Ya. Gudkova, Yu. V. Fomicheva, A. A. Kostareva, T. M. Pervunina, E. S. Vasichkina
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 3, Pp 54-59 (2018)
Barth syndrome is an X-bound inherited recessive disorder with the prevalenсe 1:300000 — 1:400000 of live bornt, caused by mutations in the gene TAZ; manifesting with dilation cardiomyopathy, neutropenia, proxymal myopathy, delayed physical and mo
Externí odkaz:
https://doaj.org/article/03d488a730434be4aa32182c11cc114a