Zobrazeno 1 - 10
of 112
pro vyhledávání: '"Zofia T, Bilińska"'
Autor:
Joanna Zakrzewska‐Koperska, Zofia T. Bilińska, Grażyna T. Truszkowska, Maria Franaszczyk, Waldemar Elikowski, Grzegorz Warmiński, Katarzyna Kalin, Piotr Urbanek, Robert Bodalski, Michał Orczykowski, Łukasz Szumowski, Rafał Płoski, Maria Bilińska
Publikováno v:
ESC Heart Failure, Vol 7, Iss 6, Pp 4326-4335 (2020)
Abstract SCN5A gene mutations are described in 2% of patients with dilated cardiomyopathy (DCM) and different rhythm disturbances, including multifocal ectopic Purkinje‐related premature contractions. Recent data indicate that sodium channel blocke
Externí odkaz:
https://doaj.org/article/9feb0a2f755e45abb217607ddc24d72f
Autor:
Przemysław Chmielewski, Grażyna Truszkowska, Ilona Kowalik, Małgorzata Rydzanicz, Ewa Michalak, Małgorzata Sobieszczańska-Małek, Maria Franaszczyk, Piotr Stawiński, Małgorzata Stępień-Wojno, Artur Oręziak, Michał Lewandowski, Przemysław Leszek, Maria Bilińska, Tomasz Zieliński, Rafał Płoski, Zofia T. Bilińska
Publikováno v:
Diagnostics, Vol 12, Iss 1, p 13 (2021)
Titin truncating variants (TTNtv) are known as the leading cause of inherited dilated cardiomyopathy (DCM). Nevertheless, it is unclear whether circulating cardiac biomarkers are helpful in detection and risk assessment. We sought to assess 1) early
Externí odkaz:
https://doaj.org/article/54e9724ff6f042be80dc9073f8cf5bb3
Autor:
Agnieszka Ługowska, Joanna K. Purzycka-Olewiecka, Rafał Płoski, Grażyna Truszkowska, Maciej Pronicki, Paulina Felczak, Mateusz Śpiewak, Aleksandra Podlecka-Piętowska, Martyna Sitek, Zofia T. Bilińska, Przemysław Leszek, Małgorzata Bednarska-Makaruk
Publikováno v:
Life, Vol 12, Iss 1, p 3 (2021)
We report on a 36-year-old man with cerebellar-extrapyramidal syndrome and severe heart failure because of dilated cardiomyopathy of unknown origin. Dysarthria and cardiac arrhythmia began at early childhood (4 years of age). Brain MRI (28 years of a
Externí odkaz:
https://doaj.org/article/d76e2f46eaf448258d98081a03af4459
Autor:
Mateusz Śpiewak, Mariusz Kłopotowski, Monika Gawor, Agata Kubik, Ewa Kowalik, Barbara Miłosz-Wieczorek, Maciej Dąbrowski, Konrad Werys, Łukasz Mazurkiewicz, Katarzyna Kożuch, Magdalena Polańska-Skrzypczyk, Joanna Petryka-Mazurkiewicz, Anna Klisiewicz, Zofia T. Bilińska, Jacek Grzybowski, Adam Witkowski, Magdalena Marczak
Publikováno v:
Journal of Cardiovascular Magnetic Resonance, Vol 19, Iss 1, Pp 1-17 (2017)
Abstract Background Cardiovascular magnetic resonance (CMR) imaging in patients with hypertrophic cardiomyopathy (HCM) enables the assessment of not only left ventricular (LV) hypertrophy and scarring but also the severity of mitral regurgitation. CM
Externí odkaz:
https://doaj.org/article/529d7a94161946f6a1646ddef999b26b
Autor:
Grażyna T. Truszkowska, Zofia T. Bilińska, Angelika Muchowicz, Agnieszka Pollak, Anna Biernacka, Katarzyna Kozar-Kamińska, Piotr Stawiński, Piotr Gasperowicz, Joanna Kosińska, Tomasz Zieliński, Rafał Płoski
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-5 (2017)
Abstract The genetic background of dilated cardiomyopathy is highly heterogeneous, with close to 100 known genes and a number of candidates described to date. Nebulin-related-anchoring protein (NRAP) is an actin-binding cytoskeletal protein expressed
Externí odkaz:
https://doaj.org/article/6446ec4421834fc0878115d8121427e5
Autor:
Przemysław Chmielewski, Grażyna T. Truszkowska, Piotr Kukla, Joanna Zakrzewska-Koperska, Mateusz Śpiewak, Małgorzata Stępień-Wojno, Maria Bilińska, Anna Lutyńska, Rafał Płoski, Zofia T. Bilińska
Publikováno v:
Diagnostics, Vol 10, Iss 11, p 955 (2020)
Mono-allelic dominant mutations in the desmoplakin gene (DSP) have been linked to known cardiac disorders, such as arrhythmogenic right ventricular cardiomyopathy and dilated cardiomyopathy. During the course of DSP cardiomyopathy, episodes of acute
Externí odkaz:
https://doaj.org/article/47641dfafe364b4595981d3017511f4c
Autor:
Hannah A. Nicolas, Anne T. Bertrand, Sarah Labib, Musfira Mohamed-Uvaize, Pierrette M. Bolongo, Wen Yu Wu, Zofia T. Bilińska, Gisèle Bonne, Marie-Andrée Akimenko, Frédérique Tesson
Publikováno v:
Cells, Vol 9, Iss 11, p 2388 (2020)
Striated muscle laminopathies are cardiac and skeletal muscle conditions caused by mutations in the lamin A/C gene (LMNA). LMNA codes for the A-type lamins, which are nuclear intermediate filaments that maintain the nuclear structure and nuclear proc
Externí odkaz:
https://doaj.org/article/b8fa30460ceb45f7a5fb18c8ea577945
Autor:
Małgorzata Stępień-Wojno, Joanna Ponińska, Elżbieta K. Biernacka, Bogna Foss-Nieradko, Tomasz Chwyczko, Paweł Syska, Rafał Płoski, Zofia T. Bilińska
Publikováno v:
Diagnostics, Vol 10, Iss 7, p 435 (2020)
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is one of causes of sudden cardiac death in the young, especially in athletes. Diagnosis of CPVT may be difficult since all cardiological examinations performed at rest are usually normal,
Externí odkaz:
https://doaj.org/article/90615f37ec434a9c93f8441db2e2e77c
Autor:
Agnieszka Ługowska, Joanna K. Purzycka-Olewiecka, Rafał Płoski, Grażyna Truszkowska, Maciej Pronicki, Paulina Felczak, Mateusz Śpiewak, Aleksandra Podlecka-Piętowska, Martyna Sitek, Zofia T. Bilińska, Przemysław Leszek, Małgorzata Bednarska-Makaruk
Publikováno v:
Life, Vol 12, Iss 3, p 3 (2022)
Life
Life
We report on a 36-year-old man with cerebellar-extrapyramidal syndrome and severe heart failure because of dilated cardiomyopathy of unknown origin. Dysarthria and cardiac arrhythmia began at early childhood (4 years of age). Brain MRI (28 years of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78f559ff311c0404d677336d8be4bc0c
https://www.mdpi.com/2075-1729/12/1/3
https://www.mdpi.com/2075-1729/12/1/3
Autor:
Philippe Charron, Benjamin Meder, Jan Haas, Grażyna Truszkowska, Mateusz Śpiewak, Hugo A. Katus, Pierre Socie, Eric Villard, Pascale Richard, Jan Koelemenoglu, Małgorzata Stępień-Wojno, Farbod Sedaghat-Hamedani, Bogna Foss-Nieradko, Weng-Tein Gi, Joanna Zakrzewska-Koperska, Elham Kayvanpour, Arjan Sammani, Ewa Michalak, Anneline S.J.M. te Riele, Folkert W. Asselbergs, Tobias Miersch, Tomasz Zieliński, Zofia T. Bilińska, Norbert Frey, Annette F. Baas, Alicia Broezel, Przemysław Chmielewski, Angelique Curjol, Rafał Płoski, David H. Lehmann
Publikováno v:
International journal of cardiology, 339, 75-82. Elsevier Ireland Ltd
Background Non-ischemic dilated cardiomyopathy (DCM) can be complicated by sustained ventricular arrhythmias (SVA) and sudden cardiac death (SCD). By now, left-ventricular ejection fraction (LV-EF) is the main guideline criterion for primary prophyla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a7333b4153b760ce466cc7d436693fe
https://doi.org/10.1016/j.ijcard.2021.07.002
https://doi.org/10.1016/j.ijcard.2021.07.002