Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ewa Czerska"'
Autor:
Karol Serwin, Andrzej Ossowski, Maria Szargut, Sandra Cytacka, Anna Urbańska, Adam Majchrzak, Anna Niedźwiedź, Ewa Czerska, Anna Pawińska-Matecka, Joanna Gołąb, Miłosz Parczewski
Publikováno v:
Viruses, Vol 13, Iss 7, p 1295 (2021)
The emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) evolved into a worldwide outbreak, with the first Polish cases in February/March 2020. This study aimed to investigate the molecular epidemiology of the circulating virus l
Externí odkaz:
https://doaj.org/article/294c421f754246b4846a30c5f5b5ed61
Autor:
Andrzej Ossowski, Anna Niedźwiedź, Ewa Czerska, Karol Serwin, Miłosz Parczewski, Sandra Cytacka, Anna Urbańska, Maria Szargut, Adam Majchrzak, Joanna Gołąb, Anna Pawinska-Matecka
Publikováno v:
Viruses
Volume 13
Issue 7
Viruses, Vol 13, Iss 1295, p 1295 (2021)
Volume 13
Issue 7
Viruses, Vol 13, Iss 1295, p 1295 (2021)
The emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) evolved into a worldwide outbreak, with the first Polish cases in February/March 2020. This study aimed to investigate the molecular epidemiology of the circulating virus l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f09e335ba4f83ce7be1b66facebddf02
Autor:
Anna Pawinska-Matecka, Krzysztof Safranow, Damir Marjanović, Amina Valjevac, Grażyna Adler, Mateusz A. Adler, Ewa Czerska, Nevena Mahmutbegović, Emir Mahmutbegovic, Iwona Ciechanowicz
Publikováno v:
Acta Informatica Medica
Introduction: Several analysis for different population conclude that endothelial plasminogen activator inhibitor 1 gene polymorphism, -675 ID, 4G/5G PAI-1 (ref SNP ID: rs1799889, also described as rs34857375, has merged into rs1799762) may increase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6befd9f4b5be2abba73932fffa8cedc1
http://europepmc.org/articles/PMC6195400
http://europepmc.org/articles/PMC6195400
Autor:
Ewa Czerska, Amina Valjevac, Nevena Mahmutbegović, Emir Mahmutbegovic, Damir Marjanović, Grażyna Adler, Edin Medjedovic, Anna Pawinska-Matecka, Agnieszka Madlani, Serkan Dogan
The relationship between genetic risk factors of thrombophilia and pregnancy loss (PL) is being discussed. The focus has been on F5 1691G>A, F2 20210G>A, and MTHFR 677C>T polymorphisms that may predispose women to microthrombosis during the stages of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::776c7fa706721397a1b07349a326e02b
https://doi.org/10.17305/bjbms.2017.1954
https://doi.org/10.17305/bjbms.2017.1954
Autor:
Emir Mahmutbegović, Damir Marjanović, Edin Medjedović, Nevena Mahmutbegović, Serkan Dogan, Amina Valjevac, Ewa Czerska, Anna Pawińska-Matecka, Agnieszka Madlani, Grażyna Adler
Publikováno v:
Bosnian Journal of Basic Medical Sciences, Vol 17, Iss 4 (2017)
The relationship between genetic risk factors of thrombophilia and pregnancy loss (PL) is being discussed. The focus has been on F5 1691G>A, F2 20210G>A, and MTHFR 677C>T polymorphisms that may predispose women to microthrombosis during the stages of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6b71ef73cf3ee9c89bf24c9a33cccf5b
https://europepmc.org/articles/PMC5708901/
https://europepmc.org/articles/PMC5708901/
Autor:
Emina Kiseljaković, Garstka Agnieszka, Ewa Czerska, Amina Valjevac, Grażyna Adler, Nermin N. Salkic
Publikováno v:
Annals of Human Biology. 42:576-580
Venous thrombosis (VT) affects 1-2 out of 10(3) individuals each year. Mutations of 1691GA FV gene, 20210GA PT gene and 677CT gene MTHFR are common in Europe and increase the risk of venous thrombosis. To the authors' knowledge, this is the first rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5893aca66fb5818fecf9f337c2a809a9
https://doi.org/10.3109/03014460.2014.968618
https://doi.org/10.3109/03014460.2014.968618
Autor:
Miłosz Parczewski, Mariusz Kaczmarczyk, Władysław Grzeszczak, Ewa Czerska, Janusz Gumprecht, A. Szybińska, Andrzej Ciechanowicz, Gail K. Adler, Beata Łoniewska, Małgorzata Mossakowska
Publikováno v:
Scopus-Elsevier
Factor V Leiden (G1691AFV mutation) is a widely acknowledged risk factor of deep vein thrombosis, including pulmonary embolism as the most serious complication. However, its high prevalence of ∼5% in the Caucasian population might be related to an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6515619cabdadf50b5090be8cc0ca211
http://www.scopus.com/inward/record.url?eid=2-s2.0-77956334516&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-77956334516&partnerID=MN8TOARS
Autor:
Andrzej Ciechanowicz, Nermin N. Salkic, Grażyna Adler, Beata Łoniewska, Jeremy Clark, Ewa Czerska
Publikováno v:
Scopus-Elsevier
ResearcherID
Web of Science
Bosnian Journal of Basic Medical Sciences, Vol 12, Iss 2 (2012)
ResearcherID
Web of Science
Bosnian Journal of Basic Medical Sciences, Vol 12, Iss 2 (2012)
The 1691G>A FV variant has been described as a common genetic risk factor in venous thromboembolism. The purpose of this study was to provide a further frequency value for 1691G>A FV in Poland and to collate summary data from Central (Poland, Czech,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cb0e37f7cd5b7d3ec38652860e2650f
http://www.scopus.com/inward/record.url?eid=2-s2.0-84861672739&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84861672739&partnerID=MN8TOARS