Please use this identifier to cite or link to this item:
http://hdl.handle.net/2445/199555
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Oliva, Antonio | - |
dc.contributor.author | Grassi, Simone | - |
dc.contributor.author | Pinchi, Vilma | - |
dc.contributor.author | Cazzato, Francesca | - |
dc.contributor.author | Coll, Mònica | - |
dc.contributor.author | Alcalde, Mireia | - |
dc.contributor.author | Vallverdú Prats, Marta | - |
dc.contributor.author | Pérez Serra, Alexandra | - |
dc.contributor.author | Martínez Barrios, Estefanía | - |
dc.contributor.author | Cesar, Sergi | - |
dc.contributor.author | Iglesias, Anna | - |
dc.contributor.author | Cruzalegui, José | - |
dc.contributor.author | Hernández, Clara | - |
dc.contributor.author | Fiol, Victoria | - |
dc.contributor.author | Arbelo, Elena | - |
dc.contributor.author | Díez Escuté, Nuria | - |
dc.contributor.author | Arena, Vincenzo | - |
dc.contributor.author | Brugada Terradellas, Josep, 1958- | - |
dc.contributor.author | Sarquella Brugada, Georgia | - |
dc.contributor.author | Brugada, Ramon | - |
dc.contributor.author | Campuzano, Óscar | - |
dc.date.accessioned | 2023-06-21T10:30:33Z | - |
dc.date.available | 2023-06-21T10:30:33Z | - |
dc.date.issued | 2022-07-28 | - |
dc.identifier.issn | 2077-0383 | - |
dc.identifier.uri | http://hdl.handle.net/2445/199555 | - |
dc.description.abstract | Brugada syndrome (BrS) is classified as an inherited cardiac channelopathy attributed to dysfunctional ion channels and/or associated proteins in cardiomyocytes rather than to structural heart alterations. However, hearts of some BrS patients exhibit slight histologic abnormalities, suggesting that BrS could be a phenotypic variant of arrhythmogenic cardiomyopathy. We performed a systematic review of the literature following Preferred Reporting Items for Systematic Reviews and Meta-Analyses Statement (PRISMA) criteria. Our comprehensive analysis of structural findings did not reveal enough definitive evidence for reclassification of BrS as a cardiomyopathy. The collection and comprehensive analysis of new cases with a definitive BrS diagnosis are needed to clarify whether some of these structural features may have key roles in the pathophysiological pathways associated with malignant arrhythmogenic episodes. | - |
dc.format.extent | 13 p. | - |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | MDPI | - |
dc.relation.isformatof | Reproducció del document publicat a: https://doi.org/10.3390/jcm11154406 | - |
dc.relation.ispartof | Journal Of Clinical Medicine, 2022, vol. 11, num. 15 | - |
dc.relation.uri | https://doi.org/10.3390/jcm11154406 | - |
dc.rights | cc by (c) Oliva, Antonio et al, 2022 | - |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.source | Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer) | - |
dc.subject.classification | Mort sobtada | - |
dc.subject.classification | Malalties del cor | - |
dc.subject.other | Sudden death | - |
dc.subject.other | Heart diseases | - |
dc.title | Structural Heart Alterations in Brugada Syndrome: Is it Really a Channelopathy? A Systematic Review | - |
dc.type | info:eu-repo/semantics/other | - |
dc.type | info:eu-repo/semantics/publishedVersion | - |
dc.date.updated | 2023-06-20T12:40:18Z | - |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | - |
dc.identifier.idimarina | 9328888 | - |
dc.identifier.pmid | 35956023 | - |
Appears in Collections: | Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer) |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
Structural Heart Alterations in Brugada Syndrome Is it Really a_ClinicalMedicine.pdf | 527.18 kB | Adobe PDF | View/Open |
This item is licensed under a
Creative Commons License