Zobrazeno 1 - 10
of 17
pro vyhledávání: '"M. 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
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:
M. E. Polyak, D. G. Podolyak, O. V. Glazova, E. A. Artyukhina, M. A. Nechaenko, E. V. Zaklyazminskaya
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 5, Pp 72-74 (2014)
Aim. To complete DNA-diagnostics for the patients with syncopes and not showing clinically significant rhythm disorders, but with family anamnesis of sudden death. Material and methods. Clinical case. The patient 22 y.o. consulted at RSCS n.a.Petrovs
Externí odkaz:
https://doaj.org/article/8a23f744e7854b0eb17c5e7fa98cb88d
Publikováno v:
European Heart Journal. 42
Introduction Noncompact myocardium (NCM) is a cardiomyopathy with various genetic causes and clinical manifestations; its relationship with other forms of dilated cardiomyopathy (DCM) and its impact on prognosis are unclear. Objective To study the pl
Autor:
Y A Lutokhina, O V Blagova, A G Shestak, M E Polyak, A A Bukaeva, E V Zaklyazminskaya, N V Varionchik, V P Sedov, E A Kogan, S A Alexandrova, A V Nedostup
Publikováno v:
European Heart Journal. 42
Background A few cases of combination of arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVC) with left ventricular noncompaction (LVNC) have been described. Aims To study the genetics, diagnostical features and clinical course of the com