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Negative screening of Fabry disease in patients with conduction disorders requiring a pacemaker
dc.contributor.author | Lopez-Sainz, Angela | |
dc.contributor.author | Climent, Vicente | |
dc.contributor.author | Ripoll-Vera, Tomas | |
dc.contributor.author | Espinosa, Maria Angeles | |
dc.contributor.author | Barriales Villa, Roberto | |
dc.contributor.author | Navarro, Marina | |
dc.contributor.author | Limeres, Javier | |
dc.contributor.author | Domingo, Diana | |
dc.contributor.author | Kasper, David C | |
dc.contributor.author | Garcia-Pavia, Pablo | |
dc.date.accessioned | 2022-01-25T12:17:35Z | |
dc.date.available | 2022-01-25T12:17:35Z | |
dc.date.issued | 2019 | |
dc.identifier.issn | 1750-1172 | |
dc.identifier.other | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615152/pdf/13023_2019_Article_1140.pdf | es |
dc.identifier.other | https://www.ncbi.nlm.nih.gov/pubmed/31286959 | es |
dc.identifier.uri | http://hdl.handle.net/20.500.11940/15925 | |
dc.description.abstract | Identification of Fabry disease (FD) in cardiac patients has been restricted so far to patients with left ventricular hypertrophy. Conduction problems are frequent in FD and could precede other manifestations, offering a possible earlier diagnosis.We studied the prevalence of FD in 188 patients < 70 years with conduction problems requiring pacemaker implantation. Although classical manifestations of FD were not rare, no patient with FD was identified. Screening efforts should not be conducted in this population. | en |
dc.language.iso | eng | es |
dc.rights | Atribución 4.0 Internacional | * |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.subject.mesh | Mutation | * |
dc.subject.mesh | Echocardiography | * |
dc.subject.mesh | Middle Aged | * |
dc.subject.mesh | Humans | * |
dc.subject.mesh | Fabry Disease | * |
dc.subject.mesh | Aged | * |
dc.title | Negative screening of Fabry disease in patients with conduction disorders requiring a pacemaker | en |
dc.type | Artigo | es |
dc.identifier.doi | 10.1186/s13023-019-1140-3 | |
dc.identifier.pmid | 31286959 | |
dc.identifier.sophos | 32387 | |
dc.issue.number | 1 | es |
dc.journal.title | Orphanet Journal of Rare Diseases | es |
dc.organization | Servizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de A Coruña - Complexo Hospitalario Universitario de A Coruña:: Cardioloxía | es |
dc.organization | Servizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::Instituto de Investigación Biomédica da Coruña (INIBIC) | es |
dc.rights.accessRights | openAccess | es |
dc.subject.decs | mutación | * |
dc.subject.decs | anciano | * |
dc.subject.decs | ecocardiografía | * |
dc.subject.decs | enfermedad de Fabry | * |
dc.subject.decs | mediana edad | * |
dc.subject.decs | humanos | * |
dc.subject.keyword | CHUAC | es |
dc.subject.keyword | INIBIC | es |
dc.typefides | Artículo Original | es |
dc.typesophos | Artículo Original | es |
dc.volume.number | 14 | es |