Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Alexandra I Ershova"'
Autor:
Alexandra I Ershova, Alexey N Meshkov, Stepan S Bazhan, Marina A Storozhok, Alexey Y Efanov, Irina V Medvedeva, Elena V Indukaeva, Yana V Danilchenko, Olga K Kuzmina, Olga L Barbarash, Alexander D Deev, Svetlana A Shalnova, Sergey A Boytsov
Publikováno v:
PLoS ONE, Vol 12, Iss 7, p e0181148 (2017)
The prevalence of familial hypercholesterolemia (FH) in Russia has not previously been evaluated. The aim of our study was to investigate the prevalence of FH in the population of the West Siberian region of Russia, and then estimate the frequency of
Externí odkaz:
https://doaj.org/article/725f2784413a4b6fbac2e1b8ee436fc8
Autor:
Alexandra I Ershova, Alexey N Meshkov, Tatyana A Rozhkova, Maria V Kalinina, Alexander D Deev, Anatoliy N Rogoza, Tatyana V Balakhonova, Sergey A Boytsov
Publikováno v:
PLoS ONE, Vol 11, Iss 7, p e0158964 (2016)
The role of plasma cholesterol in impairing arterial function and elasticity remains unclear. We evaluated arterial stiffness, measured locally in the common carotid artery by high-resolution echo-tracking, and aortic stiffness, using carotid-femoral
Externí odkaz:
https://doaj.org/article/7ddb0c6048614563a61b14a7a3e3d104
Autor:
Anastasia V. Blokhina, Alexandra I. Ershova, Anna V. Kiseleva, Evgeniia A. Sotnikova, Anastasia A. Zharikova, Marija Zaicenoka, Yuri V. Vyatkin, Vasily E. Ramensky, Vladimir A. Kutsenko, Svetlana A. Shalnova, Alexey N. Meshkov, Oxana M. Drapkina
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 17, p 13159 (2023)
Familial dysbetalipoproteinemia (FD) is a highly atherogenic genetically based lipid disorder with an underestimated actual prevalence. In recent years, several biochemical algorithms have been developed to diagnose FD using available laboratory test
Externí odkaz:
https://doaj.org/article/1ff31eb3e3684a459155ae8a3c67abaf
Autor:
Alena S. Limonova, Alexandra I. Ershova, Alexey N. Meshkov, Anna V. Kiseleva, Mikhail G. Divashuk, Marina V. Kurkina, Oxana M. Drapkina
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2022)
We reported a case of sitosterolemia, which is a rare genetic disease, characterized by increased plant sterol absorption and great heterogeneity of clinical manifestations. Our patient was initially referred to the lipid clinic due to high cholester
Externí odkaz:
https://doaj.org/article/5c21cccf1e2b488898712ae83db851c8
Autor:
Vasily E. Ramensky, Alexandra I. Ershova, Marija Zaicenoka, Anna V. Kiseleva, Anastasia A. Zharikova, Yuri V. Vyatkin, Evgeniia A. Sotnikova, Irina A. Efimova, Mikhail G. Divashuk, Olga V. Kurilova, Olga P. Skirko, Galina A. Muromtseva, Olga A. Belova, Svetlana A. Rachkova, Maria S. Pokrovskaya, Svetlana A. Shalnova, Alexey N. Meshkov, Oxana M. Drapkina
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
We performed a targeted sequencing of 242 clinically important genes mostly associated with cardiovascular diseases in a representative population sample of 1,658 individuals from the Ivanovo region northeast of Moscow. Approximately 11% of 11,876 de
Externí odkaz:
https://doaj.org/article/aa7bf729e49a4e249249cfb790f6db90
Autor:
Roman P. Myasnikov, Olga V. Kulikova, Alexey N. Meshkov, Anna A. Bukaeva, Anna V. Kiseleva, Alexandra I. Ershova, Anna V. Petukhova, Mikhail G. Divashuk, Evgenia D. Zotova, Evgeniia A. Sotnikova, Alexandra A. Abisheva, Alisa V. Muraveva, Sergey N. Koretskiy, Sergey V. Popov, Marina V. Utkina, Ekaterina A. Snigir, Sergey I. Mitrofanov, Ksenia D. Konureeva, Elena A. Mershina, Valentin E. Sinitsyn, Sergey M. Yudin, Oxana M. Drapkina
Publikováno v:
Genes, Vol 13, Iss 10, p 1750 (2022)
Variants of the MYH7 gene have been associated with a number of primary cardiac conditions, including left ventricular noncompaction cardiomyopathy (LVNC). Most cases of MYH7-related diseases are associated with such variant types as missense substit
Externí odkaz:
https://doaj.org/article/4cab55d52da44b4bacd816cc9b839d0e
Autor:
Alena S. Limonova, Alexandra I. Ershova, Alexey N. Meshkov, Anna V. Kiseleva, Mikhail G. Divashuk, Vladimir A. Kutsenko, Oxana M. Drapkina
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 7 (2021)
We present a case of a 40-year-old male with premature atherosclerosis, with evidence of both eruptive and tendinous xanthomas, which could imply an increase in both low-density lipoprotein (LDL) and triglyceride (TG) levels. However, his LDL was 2.0
Externí odkaz:
https://doaj.org/article/0b50748fd00040b899fec4263de85b6b
Autor:
Anastasia V. Blokhina, Alexandra I. Ershova, Alexey N. Meshkov, Anna V. Kiseleva, Marina V. Klimushina, Anastasia A. Zharikova, Evgeniia A. Sotnikova, Vasily E. Ramensky, Oxana M. Drapkina
Publikováno v:
Frontiers in Cardiovascular Medicine. 9
One of the most common autosomal dominant disorders is familial hypercholesterolemia (FH), causing premature atherosclerotic cardiovascular diseases and a high risk of death due to lifelong exposure to elevated low-density lipoprotein cholesterol (LD
Autor:
Evgeniia A. Sotnikova, Anna V. Kiseleva, Vladimir A. Kutsenko, Anastasia A. Zharikova, Vasily E. Ramensky, Mikhail G. Divashuk, Yuri V. Vyatkin, Marina V. Klimushina, Alexandra I. Ershova, Karina Z. Revazyan, Olga P. Skirko, Marija Zaicenoka, Irina A. Efimova, Maria S. Pokrovskaya, Oksana V. Kopylova, Anush M. Glechan, Svetlana A. Shalnova, Alexey N. Meshkov, Oxana M. Drapkina
Publikováno v:
Journal of Personalized Medicine; Volume 12; Issue 7; Pages: 1132
Cystic fibrosis, phenylketonuria, alpha-1 antitrypsin deficiency, and sensorineural hearing loss are among the most common autosomal recessive diseases, which require carrier screening. The evaluation of population allele frequencies (AF) of pathogen
Autor:
Alexey N. Meshkov, Alexandra I. Ershova, Anna V. Kiseleva, Svetlana A. Shalnova, Oxana M. Drapkina, Sergey A. Boytsov, on behalf of the FH-ESSE-RF Investigators
Publikováno v:
Journal of Personalized Medicine, Vol 11, Iss 464, p 464 (2021)
Journal of Personalized Medicine
Volume 11
Issue 6
Journal of Personalized Medicine
Volume 11
Issue 6
Heterozygous familial hypercholesterolemia (HeFH) is one of the most common genetic conditions but remains substantially underdiagnosed. The aim of our study was to investigate the prevalence of HeFH in the population of 11 different regions of Russi