Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Anna CHALOUPKA"'
Autor:
Jiri Gurka, Lenka Piherova, Filip Majer, Anna Chaloupka, Daniela Zakova, Ondrej Pelak, Alice Krebsova, Petr Peichl, Jan Krejci, Tomas Freiberger, Vojtech Melenovsky, Josef Kautzner, Tomas Kalina, Jakub Sikora, Milos Kubanek
Publikováno v:
ESC Heart Failure, Vol 7, Iss 5, Pp 2534-2543 (2020)
Abstract Aims Danon disease (DD) is a rare X‐linked disorder caused by mutations in the lysosomal‐associated membrane protein type 2 gene (LAMP2). DD is difficult to distinguish from other causes of dilated or hypertrophic cardiomyopathy (HCM) in
Externí odkaz:
https://doaj.org/article/f82c5a15de5141a49aaf81de1fa209bd
Autor:
Anna Chaloupka, Lenka Piherova, Ilga Grochova, Jana Binova, Jan Krejci, Lenka Spinarova, Viktor Stranecky, Stanislav Kmoch, Milos Kubanek
Publikováno v:
Biomedical Papers, Vol 163, Iss 4, Pp 309-317 (2019)
Aims: Recent-onset dilated cardiomyopathy (RODCM) is a disease of heterogeneous aetiology and clinical outcome. In this pilot study, we aimed to assess its genetic architecture and correlate genotype with left ventricular reverse remodelling (LVRR).
Externí odkaz:
https://doaj.org/article/40cbca6276094a469dbcdfcec4cd3314
Publikováno v:
Vnitřní lékařství. 69:89-104
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de27141decb7b8c484a6b5d2a3811b8b
https://doi.org/10.36290/vnl.2023.016
https://doi.org/10.36290/vnl.2023.016
Autor:
Lucie MAYEROVA, Anna CHALOUPKA, Peter WOHLFAHRT, Jaroslav Alois HUBACEK, Helena BEDANOVA, Zhi CHEN, Josef KAUTZNER, Vojtech MELENOVSKY, Ivan MALEK, Ales TOMASEK, Eva OZABALOVA, Jan KREJCI, Tomas KOVARNIK, Milan SONKA, Michal PAZDERNIK
Publikováno v:
Bratislavske lekarske listy.
The association between genetic polymorphisms and early cardiac allograft vasculopathy (CAV) development is relatively unexplored. Identification of genes involved in the CAV process may offer new insights into pathophysiology and lead to a wider ran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f93943b17605b74fa1a2bf1974a1cf6
https://pubmed.ncbi.nlm.nih.gov/36598310
https://pubmed.ncbi.nlm.nih.gov/36598310
Autor:
Anna Chaloupka
Publikováno v:
Cor et Vasa. 62:373-378
Dilatacni kardiomyopatie a myokarditida jsou spojeny se zvýseným rizikem srdecnich arytmii a jsou jednou z hlavnich přicin nahle srdecni smrti sportovců mladsich 35 let. Adaptace srdce na intenzivni fyzickou zatěž je sama o sobě spojena s řad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03ab31c088cad1ccea06103351d82a00
https://doi.org/10.33678/cor.2020.051
https://doi.org/10.33678/cor.2020.051
Autor:
Alice Krebsová, Vojtech Melenovsky, Lenka Piherová, Petr Peichl, Ondrej Pelak, Jakub Sikora, Tomáš Freiberger, Filip Majer, Daniela Zakova, Anna Chaloupka, Jiri Gurka, Josef Kautzner, Jan Krejčí, Tomas Kalina, Milos Kubanek
Publikováno v:
ESC Heart Failure, Vol 7, Iss 5, Pp 2534-2543 (2020)
Aims Danon disease (DD) is a rare X‐linked disorder caused by mutations in the lysosomal‐associated membrane protein type 2 gene (LAMP2). DD is difficult to distinguish from other causes of dilated or hypertrophic cardiomyopathy (HCM) in female p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dd518ee4a570392b1c1b6317997cbb3
https://doi.org/10.1002/ehf2.12823
https://doi.org/10.1002/ehf2.12823
Autor:
Jan Krejčí, Milos Kubanek, Lenka Špinarová, Anna Chaloupka, Lenka Piherová, Ilga Grochová, Jana Bínová, Viktor Stranecky, Stanislav Kmoch
Publikováno v:
Biomedical Papers, Vol 163, Iss 4, Pp 309-317 (2019)
Aims: Recent-onset dilated cardiomyopathy (RODCM) is a disease of heterogeneous aetiology and clinical outcome. In this pilot study, we aimed to assess its genetic architecture and correlate genotype with left ventricular reverse remodelling (LVRR).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44a8a093d0c77163d8f1cbf70684c13b
https://biomed.papers.upol.cz/artkey/bio-201904-0004_genetic-architecture-of-recent-onset-dilated-cardiomyopathy-in-moravian-region-assessed-by-whole-exome-sequenci.php
https://biomed.papers.upol.cz/artkey/bio-201904-0004_genetic-architecture-of-recent-onset-dilated-cardiomyopathy-in-moravian-region-assessed-by-whole-exome-sequenci.php
Autor:
Alberto Aimo, Colin E. Evans, Michael Cooklin, Gerald Carr-White, Georgios Georgiopoulos, Silvia Molaro, Pier-Giorgio Masci, N Sheikh, Mattia Zampieri, Leema Roberts, Rachel Bastiaenen, Amedeo Chiribiri, Anna Chaloupka, Gherardo Finocchiaro, Barbara Barra, Laura Monje-Garcia
Publikováno v:
The International Journal of Cardiovascular Imaging
Left ventricular (LV) involvement in patients with arrhythmogenic right ventricular cardiomyopathy (ARVC) is not evaluated in the revised Task Force Criteria, possibly leading to underdiagnosis. This study explored the diagnostic role of myocardial n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc2fbaaf09b7458291bb707aecf4086f
https://doi.org/10.1007/s10554-021-02166-7
https://doi.org/10.1007/s10554-021-02166-7
Publikováno v:
Cor et Vasa. 59:e424-e429
Cil: Hypertroficka kardiomyopatie (HKMP) je poměrně caste, geneticky podminěne srdecni onemocněni (vyskytujici se s prevalenci 1 : 500), ktere je ve svem klinickem obraze, prognoze a lecebných strategiich znacně heterogenni. Jako takove casto p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f72671cfad6262eb76411cbfef22b57
https://doi.org/10.1016/j.crvasa.2016.08.004
https://doi.org/10.1016/j.crvasa.2016.08.004
Autor:
I Grochova, Milos Kubanek, Stanislav Kmoch, Jan Krejčí, Viktor Stranecky, J Binova, Anna Chaloupka, Lenka Špinarová, Lenka Piherová
Publikováno v:
European Heart Journal. 40
Background Recent-onset dilated cardiomyopathy (RODCM) is a disease of heterogeneous aetiology including genetic, inflammatory, toxic and metabolic causes. Recognition of the genetic component could improve diagnostic management and risk stratificati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0459d9d9657490684e866604624267a8
https://doi.org/10.1093/eurheartj/ehz746.1044
https://doi.org/10.1093/eurheartj/ehz746.1044