P12—Fabry Disease in Latin America: A Report From the Fabry Registry
Fabry disease is a rare lysosomal storage disorder caused by a deficient activity of the lysosomal enzyme ?-galactosidase A. The Fabry Registry is a global, observational, and voluntary program designed to collect clinical data related to the onset, progression, and treatment of Fabry disease.
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2012
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/25950
- Acceso en línea:
- https://doi.org/10.1016/j.clinthera.2012.03.042
https://repository.urosario.edu.co/handle/10336/25950
- Palabra clave:
- Medical and Health Sciences
Pharmacology and Pharmaceutical Sciences
- Rights
- License
- Restringido (Acceso a grupos específicos)
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5821e96e-9e07-4d26-a6bb-eb4c08ef27c3-146d50aa4-bb54-49ae-860b-89b7a9645c28-1ca2d60ff-2ea4-496e-8bb1-1b5091cf65ec-10b9c6165-e144-4aa3-92b0-68b6f4f1187b-1f9bf9a35-2889-4ccb-90bb-003f7b226daf-11730e91a-3ada-408a-8913-9c2eeb35e34b-12020-08-06T16:20:18Z2020-08-06T16:20:18Z2012-04-01Fabry disease is a rare lysosomal storage disorder caused by a deficient activity of the lysosomal enzyme ?-galactosidase A. The Fabry Registry is a global, observational, and voluntary program designed to collect clinical data related to the onset, progression, and treatment of Fabry disease.application/pdfhttps://doi.org/10.1016/j.clinthera.2012.03.042ISSN: 1521-7035EISSN: 1521-6616https://repository.urosario.edu.co/handle/10336/25950engElsevierNo. 4e23 Clinical TherapeuticsVol. 34Clinical Therapeutics, ISSN:1521-7035 ; EISSN:1521-6616, Vol.34, No.4 (April, 2012); pp.e23https://www.clinicaltherapeutics.com/article/S0149-2918(12)00192-0/fulltextRestringido (Acceso a grupos específicos)http://purl.org/coar/access_right/c_16ecClinical Therapeuticsinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURMedical and Health SciencesPharmacology and Pharmaceutical SciencesP12—Fabry Disease in Latin America: A Report From the Fabry RegistryP12 — Enfermedad de Fabry en América Latina: un informe del registro de FabryarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Martins, A.M.Ospina, S.Villalobos, J.Politei, J.Varas, C.Registry Coordinators, Latin America10336/25950oai:repository.urosario.edu.co:10336/259502021-06-03 00:50:22.146https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |
dc.title.spa.fl_str_mv |
P12—Fabry Disease in Latin America: A Report From the Fabry Registry |
dc.title.TranslatedTitle.spa.fl_str_mv |
P12 — Enfermedad de Fabry en América Latina: un informe del registro de Fabry |
title |
P12—Fabry Disease in Latin America: A Report From the Fabry Registry |
spellingShingle |
P12—Fabry Disease in Latin America: A Report From the Fabry Registry Medical and Health Sciences Pharmacology and Pharmaceutical Sciences |
title_short |
P12—Fabry Disease in Latin America: A Report From the Fabry Registry |
title_full |
P12—Fabry Disease in Latin America: A Report From the Fabry Registry |
title_fullStr |
P12—Fabry Disease in Latin America: A Report From the Fabry Registry |
title_full_unstemmed |
P12—Fabry Disease in Latin America: A Report From the Fabry Registry |
title_sort |
P12—Fabry Disease in Latin America: A Report From the Fabry Registry |
dc.subject.keyword.spa.fl_str_mv |
Medical and Health Sciences Pharmacology and Pharmaceutical Sciences |
topic |
Medical and Health Sciences Pharmacology and Pharmaceutical Sciences |
description |
Fabry disease is a rare lysosomal storage disorder caused by a deficient activity of the lysosomal enzyme ?-galactosidase A. The Fabry Registry is a global, observational, and voluntary program designed to collect clinical data related to the onset, progression, and treatment of Fabry disease. |
publishDate |
2012 |
dc.date.created.spa.fl_str_mv |
2012-04-01 |
dc.date.accessioned.none.fl_str_mv |
2020-08-06T16:20:18Z |
dc.date.available.none.fl_str_mv |
2020-08-06T16:20:18Z |
dc.type.eng.fl_str_mv |
article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.spa.spa.fl_str_mv |
Artículo |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.1016/j.clinthera.2012.03.042 |
dc.identifier.issn.none.fl_str_mv |
ISSN: 1521-7035 EISSN: 1521-6616 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/25950 |
url |
https://doi.org/10.1016/j.clinthera.2012.03.042 https://repository.urosario.edu.co/handle/10336/25950 |
identifier_str_mv |
ISSN: 1521-7035 EISSN: 1521-6616 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.citationIssue.none.fl_str_mv |
No. 4 |
dc.relation.citationStartPage.none.fl_str_mv |
e23 |
dc.relation.citationTitle.none.fl_str_mv |
Clinical Therapeutics |
dc.relation.citationVolume.none.fl_str_mv |
Vol. 34 |
dc.relation.ispartof.spa.fl_str_mv |
Clinical Therapeutics, ISSN:1521-7035 ; EISSN:1521-6616, Vol.34, No.4 (April, 2012); pp.e23 |
dc.relation.uri.spa.fl_str_mv |
https://www.clinicaltherapeutics.com/article/S0149-2918(12)00192-0/fulltext |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_16ec |
dc.rights.acceso.spa.fl_str_mv |
Restringido (Acceso a grupos específicos) |
rights_invalid_str_mv |
Restringido (Acceso a grupos específicos) http://purl.org/coar/access_right/c_16ec |
dc.format.mimetype.none.fl_str_mv |
application/pdf |
dc.publisher.spa.fl_str_mv |
Elsevier |
dc.source.spa.fl_str_mv |
Clinical Therapeutics |
institution |
Universidad del Rosario |
dc.source.instname.none.fl_str_mv |
instname:Universidad del Rosario |
dc.source.reponame.none.fl_str_mv |
reponame:Repositorio Institucional EdocUR |
repository.name.fl_str_mv |
Repositorio institucional EdocUR |
repository.mail.fl_str_mv |
edocur@urosario.edu.co |
_version_ |
1814167667262619648 |