Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Alexandra Klyushina"'
Autor:
Olga Kofeynikova, Daria Alekseeva, Tatiana Vershinina, Svetlana Fetisova, Olga Peregudina, Tatiana Kovalchuk, Elena Yakovleva, Polina Sokolnikova, Alexandra Klyushina, Kseniia Chueva, Anna Kostareva, Tatiana Pervunina, Elena Vasichkina
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
IntroductionThe present study aimed to describe the phenotypic features and genetic spectrum of arrhythmogenic cardiomyopathy (ACM) presented in childhood and test the validity of different diagnostic approaches using Task Force Criteria 2010 (TFC) a
Externí odkaz:
https://doaj.org/article/1655c203a98949849ab3c83f9cee4a9b
Autor:
Anna Kostareva, Artem Kiselev, Alexandra Gudkova, Goar Frishman, Andreas Ruepp, Dmitrij Frishman, Natalia Smolina, Svetlana Tarnovskaya, Daniel Nilsson, Anna Zlotina, Tatiana Khodyuchenko, Tatiana Vershinina, Tatiana Pervunina, Alexandra Klyushina, Andrey Kozlenok, Gunnar Sjoberg, Irina Golovljova, Thomas Sejersen, Eugeniy Shlyakhto
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0163362 (2016)
BACKGROUND:Cardiomyopathies represent a rare group of disorders often of genetic origin. While approximately 50% of genetic causes are known for other types of cardiomyopathies, the genetic spectrum of restrictive cardiomyopathy (RCM) is largely unkn
Externí odkaz:
https://doaj.org/article/764033b189314c3c94b73bc07e66efb8
Autor:
Polina Popova, Aleksandra Tkachuk, Alexandra Klyushina, Lyudmila Vasilyeva, Elena Vasukova, Anna Anopova, Evgenii Pustozerov, Yana Teplova, Elena Grineva
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3399202e64a051d79f93494b9a5dba29
https://doi.org/10.1530/endoabs.81.ep917
https://doi.org/10.1530/endoabs.81.ep917
Autor:
Alexandra Klyushina, Anna Kostareva, Yana Bolotko, Polina V. Popova, Ekaterina N. Kravchuk, Andrey Gerasimov, Lyudmila B. Vasilyeva, Alexandra S. Tkachuk, Evgenii Pustozerov, Elena N. Grineva, Alexander V. Predeus
Publikováno v:
Oncotarget
// Polina V. Popova 1, 2 , Alexandra A. Klyushina 1 , Lyudmila B. Vasilyeva 1 , Alexandra S. Tkachuk 1 , Yana A. Bolotko 1 , Andrey S. Gerasimov 1 , Evgenii A. Pustozerov 1, 3 , Ekaterina N. Kravchuk 1 , Alexander Predeus 4, 5 , Anna A. Kostareva 1,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b1ded004ecc7b89ea5236b697af0264
https://doi.org/10.18632/oncotarget.22999
https://doi.org/10.18632/oncotarget.22999
Autor:
Anna Kostareva, Alexandra S. Tkachuk, Polina Popova, Yana Bolotko, Alexandra Klyushina, Andrey Gerasimov, Elena Grineva
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84f0601bf1bf5d20523ef81a7cb5ced8
https://doi.org/10.1530/endoabs.49.gp78
https://doi.org/10.1530/endoabs.49.gp78
Autor:
Gunnar Sjöberg, Anna Kostareva, Olga Freylikhman, Sergey Zhuk, Tatyana Tatarinova, Olga Moiseeva, Alexandra Klyushina, Anna Malashicheva, Natalia Smolina, Artem Kiselev
Publikováno v:
Congenital Heart Disease. 9:391-396
Background and Objective Malformations of the left ventricular outflow tract are one of the most common forms of congenital heart disorders. Recently, it has been shown that mutations in the NOTCH1 gene can lead to bicuspid aortic valve, aortic aneur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f571d061443ef9709f9901ece1b27ba5
https://doi.org/10.1111/chd.12157
https://doi.org/10.1111/chd.12157
Autor:
Gunnar Sjöberg, Artem Kiselev, Tatiana Pervunina, Tatiana Khodyuchenko, Andreas Ruepp, A Gudkova, Eugeniy Shlyakhto, S. I. Tarnovskaya, Daniel Nilsson, Goar Frishman, Dmitrij Frishman, Alexandra Klyushina, Anna Zlotina, Natalia Smolina, Tatiana Vershinina, Andrey Kozlenok, Thomas Sejersen, Irina Golovljova, Anna Kostareva
Publikováno v:
PLoS ONE 11:e0163362 (2016)
PLoS ONE
PLoS ONE, Vol 11, Iss 9, p e0163362 (2016)
PLoS ONE
PLoS ONE, Vol 11, Iss 9, p e0163362 (2016)
Background Cardiomyopathies represent a rare group of disorders often of genetic origin. While approximately 50% of genetic causes are known for other types of cardiomyopathies, the genetic spectrum of restrictive cardiomyopathy (RCM) is largely unkn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef31189159304b541e605db0e40c1b10
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=49543
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=49543
Autor:
Olga, Freylikhman, Tatyana, Tatarinova, Natalia, Smolina, Sergey, Zhuk, Alexandra, Klyushina, Artem, Kiselev, Olga, Moiseeva, Gunnar, Sjoberg, Anna, Malashicheva, Anna, Kostareva
Publikováno v:
Congenital heart disease. 9(5)
Malformations of the left ventricular outflow tract are one of the most common forms of congenital heart disorders. Recently, it has been shown that mutations in the NOTCH1 gene can lead to bicuspid aortic valve, aortic aneurysm, and hypoplastic left
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3cfed257fdfd34d524d967370ed44fae
https://pubmed.ncbi.nlm.nih.gov/24418111
https://pubmed.ncbi.nlm.nih.gov/24418111