Zobrazeno 1 - 10
of 125
pro vyhledávání: '"E, Polyak"'
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
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
Abstract Background Inherited deficiency of the antithrombin (hereditary antithrombin deficiency, AT deficiency, OMIM #613118) is a relatively rare (1:2000–3000) autosomal-dominant disorder with high risk of venous thromboembolism. Mutations in the
Externí odkaz:
https://doaj.org/article/da72a02d26ee4da19edf87a0f6ed54a9
Autor:
E. V. Pavlenko, O. V. Blagova, N. V. Varionchik, A. V. Nedostup, V. P. Sedov, M. E. Polyak, E. V. Zaklyazminskaya
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 2, Pp 12-25 (2019)
Aim. To study clinical forms of noncompact myocardium (NCM) in adults, the features of their manifestation, course and progression.Material and methods. The study included 116 adult patients with NCM of the left ventricle (LV) (67 men, mean age 46,3
Externí odkaz:
https://doaj.org/article/f24cf50070634647b3e22339d4d387ba
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 2, Pp 106-113 (2017)
The left ventricle non-compaction myocardium syndrome is relatively new diagnosis entered clinical practice with improvement of the heart visualization methods. There is plenty of studies on genetic heterogeneity of non-compaction myocardium syndrome
Externí odkaz:
https://doaj.org/article/1aa94356b1f54727b9564946bf943c18
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 15-20 (2016)
The primary long QT syndrome (LQTS) is hereditary disorder of cardiac rhythm. More than 15 genetic types of the disease known. Most prevalent is the type of the disorder related to potassium channel KvLQT1.Aim. Analysis of mutation spectrum in the ge
Externí odkaz:
https://doaj.org/article/21fde71b181c441d9c8ec6943b5856af
Autor:
M. E. Polyak, A. A. Bukaeva, A. G. Shestak, O. V. Blagova, A. V. Sveshnikov, Yu. A. Lutokhina, A. V. Nedostup, E. V. Zaklyazminakaya
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 98-104 (2016)
Non-compaction myocardium syndrome of the left ventricle (NCM) is relatively new diagnosis. There is no consensual approach to classification, diagnostics, as treatment and management of patients with NCM till recently. Predictive value of the observ
Externí odkaz:
https://doaj.org/article/4720e8f75c0b43ac94a48fb8113bd4d4
Autor:
Yu. V. Frolova, O. V. Dymova, E. V. Zaklyazminskaya, M. E. Polyak, E. A. Mershina, V. E. Sinitsin, S. L. Dzemeshkevich
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 2, Pp 100-102 (2017)
First time, myocardial clefty were described more than 20 years ago in autopsy of patients with hypertrophic cardiomyopathy (HCMP): the “fissure” along muscle fibers in interventricular septum. Currently, the precise diagnostical and practical va
Externí odkaz:
https://doaj.org/article/259303692175432fb076a8dccf2c5f26
Autor:
Andrey K. Tsaturyan, Elena V. Zaklyazminskaya, Margarita E. Polyak, Galina V. Kopylova, Daniil V. Shchepkin, Anastasia M. Kochurova, Anastasiia D. Gonchar, Sergey Y. Kleymenov, Natalia A. Koubasova, Sergey Y. Bershitsky, Alexander M. Matyushenko, Dmitrii I. Levitsky
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 1; Pages: 18
Hypertrophic cardiomyopathy (HCM), caused by mutations in thin filament proteins, manifests as moderate cardiac hypertrophy and is associated with sudden cardiac death (SCD). We identified a new de novo variant, c.656A>T (p.D219V), in the TPM1 gene e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afe4d2e3cb8bb53b1fdeba5b061fffac
Autor:
L. E. Polyak, V. I. Mikhaylov
Publikováno v:
Journal of Surface Investigation: X-ray, Synchrotron and Neutron Techniques. 15:683-695
The adsorption of Cd and Te on the surface of a CdTe crystal is studied in situ using a mass spectrometer in the temperature range of 500−700 K and at an incident flux intensity of VCd = 10–2−2 single layers per second, SL/s, and VTe = 0.5−5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7dc30ade61b812227f267f4286e1ffe
https://doi.org/10.1134/s1027451021040133
https://doi.org/10.1134/s1027451021040133
Publikováno v:
In Value in Health June 2024 27(6) Supplement:S339-S339