dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
dc.contributor.author | Demolder, Anthony |
dc.contributor.author | Bianco, Lisa |
dc.contributor.author | Caruanac, Maryanne |
dc.contributor.author | Cervi, Elena |
dc.contributor.author | Evangelista Masip, Artur |
dc.contributor.author | Jondeau, Guillaume |
dc.contributor.author | López Sainz, Angela |
dc.contributor.author | Sabaté Rotés Anna |
dc.contributor.author | Teixido Tura, Gisela |
dc.date.accessioned | 2022-09-07T12:22:02Z |
dc.date.available | 2022-09-07T12:22:02Z |
dc.date.issued | 2022-06 |
dc.identifier.citation | Demolder A, Bianco L, Caruana M, Cervi E, Evangelista A, Jondeau G, et al. Arrhythmia and impaired myocardial function in heritable thoracic aortic disease: An international retrospective cohort study. Eur J Med Genet. 2022 Jun;65(6):104503. |
dc.identifier.issn | 1660-4601 |
dc.identifier.uri | https://hdl.handle.net/11351/8059 |
dc.description | Arrítmia; Malaltia hereditària de l'aorta toràcica |
dc.language.iso | eng |
dc.publisher | Elsevier |
dc.relation.ispartofseries | European Journal of Medical Genetics;65(6) |
dc.rights | Attribution 4.0 International |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ |
dc.source | Scientia |
dc.subject | Arrítmia |
dc.subject | Aorta - Malalties - Complicacions |
dc.subject | Malalties congènites |
dc.subject.mesh | Aortic Diseases |
dc.subject.mesh | /complications |
dc.subject.mesh | Arrhythmias, Cardiac |
dc.title | Arrhythmia and impaired myocardial function in heritable thoracic aortic disease: An international retrospective cohort study |
dc.type | info:eu-repo/semantics/article |
dc.identifier.doi | 10.1016/j.ejmg.2022.104503 |
dc.subject.decs | enfermedades de la aorta |
dc.subject.decs | /complicaciones |
dc.subject.decs | arritmias cardíacas |
dc.relation.publishversion | https://doi.org/10.1016/j.ejmg.2022.104503 |
dc.type.version | info:eu-repo/semantics/publishedVersion |
dc.audience | Professionals |
dc.contributor.organismes | Institut Català de la Salut |
dc.contributor.authoraffiliation | [Demolder A] Centre for Medical Genetics, Ghent University Hospital, Ghent, Belgium. Department of Cardiology, Ghent University Hospital, Ghent, Belgium. [Bianco L, Sabaté-Rotés A] Servei de Cardiologia Pediàtrica, Vall d'Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. [Caruana M] Department of Cardiology, Mater Dei Hospital, Birkirkara Bypass, Malta. VASCERN HTAD Affiliated Partner Centre, Austria. [Cervi E] Centre for Inherited Cardiovascular Diseases, Great Ormond Street Hospital, London, UK. [Evangelista A, López-Sainz Á, Teixidó-Tura G] Servei de Cardiologia, Vall d'Hebron Hospital Universitari, Barcelona, Spain. Vall d'Hebron Institut de Recerca (VHIR), Barcelona, Spain. CIBER-CV, Barcelona, Spain. VASCERN HTAD European Reference Centre, Belgium. [Jondeau G] VASCERN HTAD European Reference Centre, Belgium. Centre de référence pour le syndrome de Marfan et apparentés, AP-HP, Hôpital Bichat, Paris, France |
dc.identifier.pmid | 35427808 |
dc.identifier.wos | 000821505600002 |
dc.rights.accessrights | info:eu-repo/semantics/openAccess |