dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
dc.contributor.author | van de Laar, Ingrid M. B. H. |
dc.contributor.author | Arbustini, Eloisa |
dc.contributor.author | Loeys, Bart |
dc.contributor.author | Björck, Erik |
dc.contributor.author | Murphy, Lise |
dc.contributor.author | Groenink, Maarten |
dc.contributor.author | Teixido Tura, Gisela |
dc.contributor.author | Evangelista Masip, Artur |
dc.date.accessioned | 2021-04-12T07:05:04Z |
dc.date.available | 2021-04-12T07:05:04Z |
dc.date.issued | 2019-11-21 |
dc.identifier.citation | van de Laar IMBH, Arbustini E, Loeys B, Björck E, Murphy L, Groenink M, et al. European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants. Orphanet J Rare Dis. 2019 Nov 21;14(1):264. |
dc.identifier.issn | 1750-1172 |
dc.identifier.uri | https://hdl.handle.net/11351/5836 |
dc.description | Malaltia aòrtica; Dissecció; Aneurisma aòrtic toràcic |
dc.description.sponsorship | This work was supported by the Dutch Heart Foundation (2014 T007) and by an Erasmus University Rotterdam Fellowship (I.M.B.H. van de Laar). |
dc.language.iso | eng |
dc.publisher | BMC |
dc.relation.ispartofseries | Orphanet Journal of Rare Diseases;14(1) |
dc.rights | Attribution 4.0 International |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ |
dc.source | Scientia |
dc.subject | Aneurismes aòrtics |
dc.subject | Malalties rares |
dc.subject | Genètica |
dc.subject.mesh | Rare Diseases |
dc.subject.mesh | Aortic Aneurysm, Thoracic |
dc.subject.mesh | /genetics |
dc.title | European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants |
dc.type | info:eu-repo/semantics/article |
dc.identifier.doi | 10.1186/s13023-019-1186-2 |
dc.subject.decs | enfermedades raras |
dc.subject.decs | aneurisma de la aorta torácica |
dc.subject.decs | /genética |
dc.relation.publishversion | https://ojrd.biomedcentral.com/articles/10.1186/s13023-019-1186-2 |
dc.type.version | info:eu-repo/semantics/publishedVersion |
dc.audience | Professionals |
dc.contributor.organismes | Institut Català de la Salut |
dc.contributor.authoraffiliation | [van de Laar IMBH] Department of Clinical Genetics and Cardiology and VASCERN HTAD European Reference Centre, Erasmus MC, University Medical Center Rotterdam, Wytemaweg 80, P.O. Box 2040, 3000 CA Rotterdam, The Netherlands. VASCERN HTAD European Reference Centre, Ghent, Belgium. [Arbustini E] VASCERN HTAD European Reference Centre, Ghent, Belgium. Center for Inherited Cardiovascular Diseases and VASCERN HTAD European Reference Centre, IRCCS Foundation Policlinico San Matteo, Pavia, Italy. [Loeys B] VASCERN HTAD European Reference Centre, Ghent, Belgium. Center of Medical Genetics and VASCERN HTAD European Reference Centre, University Hospital of Antwerp University of Antwerp, Antwerp, Belgium. Department of Clinical Genetics and Cardiology and VASCERN HTAD European Reference Centre, Radboud university medical center, Nijmegen, Netherlands. [Björck E] VASCERN HTAD European Reference Centre, Ghent, Belgium. Department of Clinical Genetics and Department of Molecular medicine and Surgery and VASCERN HTAD European Reference Centre, Karolinska University Hospital, Karolinska Institute, Stockholm, Sweden. [Murphy L] VASCERN Patient Group (ePAG) and Swedish Marfan organization and VASCERN HTAD European Reference Centre, Färjestaden, Sweden. [Groenink M] VASCERN HTAD European Reference Centre, Ghent, Belgium. Department of Cardiology, and VASCERN HTAD European Reference Centre, Academic Medical Center, Amsterdam, Netherlands. [Teixidó-Turà G, Evangelista A] VASCERN HTAD European Reference Centre. Servei de Cardiologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain |
dc.identifier.pmid | 31752940 |
dc.identifier.wos | 000509802100001 |
dc.rights.accessrights | info:eu-repo/semantics/openAccess |