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Enzyme Replacement Therapies for Lysosomal Storage Diseases

dc.contributor.authorCoutinho, Maria Francisca
dc.date.accessioned2019-03-25T14:02:36Z
dc.date.available2019-03-25T14:02:36Z
dc.date.issued2018-11
dc.description.abstractLysosomal Storage Disorders (LSDs): Genetic; Rare; Autosomal recessive (majority). Portugal - 1/4000; Almost 70!. The concept of enzyme replacement as a potential therapeutic approach to ameliorate lysosomal storage disorders (LSDs) is virtually as old as the concept of LSD itself. In fact, both concepts were established right after the first enzymatic deficiency underlying an LSD was described, and enzyme replacement therapy (ERT) remained the golden standard for LSD treatment for years. Nevertheless, its ineffectiveness to correct brain pathology, together with its high cost and lifelong dependence prompted the search for additional therapeutic approaches, which are currently being investigated: chaperone therapy; gene enhancement and gene therapy. Still, no matter how effective the treatment or cutting-edge the technology used in any of these cases, the underlying rationale is virtually the same: an attempt to provide or enhance the activity of the missing enzyme.pt_PT
dc.description.sponsorshipFCT SFRH/BPD/101965/2014; SFRH/BD/124372/2016pt_PT
dc.description.versionN/Apt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/6291
dc.language.isoengpt_PT
dc.peerreviewednopt_PT
dc.subjectLysosomal Storage Diseasespt_PT
dc.subjectEnzyme Replacement Therapypt_PT
dc.subjectDoenças Genéticaspt_PT
dc.subjectGenética Humanapt_PT
dc.titleEnzyme Replacement Therapies for Lysosomal Storage Diseasespt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceBudapest, Hungarypt_PT
oaire.citation.titleSemmelweis Symposium 2018 'New approaches in personalized medicine: From prenatal testing to targeted tumor therapy', 8-9 November 2018pt_PT
person.familyNameCoutinho
person.givenNameMaria Francisca
person.identifier.ciencia-idE211-15A7-D371
person.identifier.orcid0000-0002-2222-3622
person.identifier.scopus-author-id56350180700
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isAuthorOfPublicationb95c8c12-245a-47fb-a746-9ef1f1a15c39
relation.isAuthorOfPublication.latestForDiscoveryb95c8c12-245a-47fb-a746-9ef1f1a15c39

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