Hereditary Transthyretin Amyloidosis with Polyneuropathy: Monitoring and Management

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dc.contributor.authorVélez Santamaría, Valentina
dc.contributor.authorNedkova Hristova, Velina
dc.contributor.authorMorales de la Prida, Moisés
dc.contributor.authorCasasnovas, Carlos
dc.date.accessioned2023-02-06T08:44:27Z
dc.date.available2023-02-06T08:44:27Z
dc.date.issued2022-12-01
dc.date.updated2023-02-01T15:34:22Z
dc.description.abstractOur aim in this review is to discuss current treatments and investigational products and their effect on patients with hereditary transthyretin amyloidosis with polyneuropathy (ATTRv-PN) and provide suggestions for monitoring disease progression and treatment efficacy.
dc.format.extent8 p.
dc.format.mimetypeapplication/pdf
dc.identifier.issn8677–8684
dc.identifier.pmid36573111
dc.identifier.urihttps://hdl.handle.net/2445/193120
dc.language.isoeng
dc.publisherInforma UK Limited
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.2147/IJGM.S338430
dc.relation.ispartofInternational Journal of General Medicine, 2022, vol. 15, p. 8677-8684
dc.relation.urihttps://doi.org/10.2147/IJGM.S338430
dc.rightscc by-nc (c) Vélez Santamaría, Valentina et al., 2022
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationMalalties hereditàries
dc.subject.classificationAmiloïdosi
dc.subject.classificationAmiloides
dc.subject.classificationMonitoratge de pacients
dc.subject.otherAmyloidosis
dc.subject.otherAmyloid
dc.subject.otherGenetic diseases
dc.subject.otherPatient monitoring
dc.titleHereditary Transthyretin Amyloidosis with Polyneuropathy: Monitoring and Management
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))