Zobrazeno 1 - 10
of 52
pro vyhledávání: '"N, Chakova"'
Autor:
S. M. Komissarova, A. A. Efimova, N. N. Chakova, T. V. Dolmatovich, E. S. Rebeko, L. I. Plashchinskaya, V. Ch. Barsukevich, A. A. Gusina
Publikováno v:
Евразийский Кардиологический Журнал, Vol 0, Iss 1, Pp 78-85 (2023)
Aim. To assess the prevalence of the left ventricle involvement and the features of the biventricular phenotype of arrhythmogenic cardiomyopathy in patients with pathogenic mutations in the PKP2 and DSP genes.Material and methods. Three unrelated pro
Externí odkaz:
https://doaj.org/article/2bf280f4cb834412a8044e3cb22fee80
Publikováno v:
Евразийский Кардиологический Журнал, Vol 0, Iss 2, Pp 62-69 (2021)
Purpose. To evaluate the genotype-phenotype association in Belarusian patients with non-compaction cardiomyopathy (NCCM) and clinically significant ventricular arrhythmias.Materials and methods. The study included 170 unrelated patients with NCCM pro
Externí odkaz:
https://doaj.org/article/da9f6c58e4fa4d94b51fb1fa9b667f05
Publikováno v:
Евразийский Кардиологический Журнал, Vol 0, Iss 3, Pp 106-111 (2020)
The features of the clinical course of non-compaction cardiomyopathy, its prognosis and even its diagnosis are still the subject of discussion. The variety of phenotypes of this disease and genetic heterogeneity dictates the need for detailed clinica
Externí odkaz:
https://doaj.org/article/c632d344afc64d7b8cbc7659de4a4424
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 0, Iss 10, Pp 110-117 (2019)
Isolated glycogen storage disease of the heart (PRKAG2 syndrome) is a form of glycogenosis, which is characterized by left ventricular hypertrophy, similar to the phenotype of hypertrophic cardiomyopathy, associated with pre-excitation of the ventric
Externí odkaz:
https://doaj.org/article/54689a00e8f94e66a8a9c92b7691df79
Publikováno v:
Journal of Arrhythmology. 29:7-16
The aim of the study is to evaluate clinical characteristics, including adverse events and outcomes, in patients with various genetic types of long QT syndrome (LQTS).Material and methods. We examined 24 patients with a clinical diagnosis of LQTS, ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2dbe9dd4b67be6f8cb32f0b6988ab9b9
https://doi.org/10.35336/va-2022-1-02
https://doi.org/10.35336/va-2022-1-02
Autor:
S. M. Komissarova, N. N. Chakova, S. S. Niyazova, S. V. Kazakov, E. A. Zhukova, A. V. Aleksandrov, O. S. Glotov, A. S. Glotov
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 1, Pp 20-25 (2016)
Aim. The assessment of clinical presentation of HCMP in patients having mutations of the sarcomere protein genes.Material and methods. In 11 patients with hypertrophic cardiomyopathy (HCMP) we performed analysis of clinical and instrumental data and
Externí odkaz:
https://doaj.org/article/1b9214cbd7ed4af988cf176de52aee19
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 6, Pp 75-80 (2015)
Aim. To reveal the associations of polymorphic genes variants coding the proteins of sympathoadrenal system (ADRB1 and ADRB2) with clinical phenotype of the disease including age and gender of patients with HCMP.Material and methods. The analysis of
Externí odkaz:
https://doaj.org/article/166074b33d6949a28658ab00ad6608a9
Autor:
S. M. Komissarova, N. M. Rineiskaya, N. N. Chakova, A. A. Efimova, T. V. Dolmatovich, S. S. Niyazova
Publikováno v:
The Siberian Journal of Clinical and Experimental Medicine.
Aim. Evaluate clinical and structural-functional characteristics, including adverse events and outcomes, in patients with non-compact cardiomyopathy (NCM) with various genetic variants.Material and Methods. 51 unrelated patients with NCM were examine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0520d4647e510ff082cb35cbc5f23029
https://doi.org/10.29001/2073-8552-2022-430
https://doi.org/10.29001/2073-8552-2022-430
Publikováno v:
Kardiologiia. 60:137-145
Aim To study the clinical course of the mixed phenotype (hypertrophic cardiomyopathy, HCMP, and left ventricular noncompaction, LVNC); to determine its genetic causes; and to evaluate incidence of cardiovascular complications (CVC) during the follow-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44c286b217558d20f0c159aff192bef2
https://doi.org/10.18087/cardio.2020.4.n728
https://doi.org/10.18087/cardio.2020.4.n728