Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/113457
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dc.contributor.authorSantana, Magda M.-
dc.contributor.authorGaspar, Laetitia S.-
dc.contributor.authorPinto, Maria M.-
dc.contributor.authorSilva, Patrick Joel da-
dc.contributor.authorAdão, Diana-
dc.contributor.authorPereira, Dina-
dc.contributor.authorRibeiro, Joana Afonso-
dc.contributor.authorCunha, Inês-
dc.contributor.authorHuebener-Schmid, Jeannette-
dc.contributor.authorRaposo, Mafalda-
dc.contributor.authorFerreira, Ana F.-
dc.contributor.authorFaber, Jennifer-
dc.contributor.authorKuhs, Sandra-
dc.contributor.authorGarcia-Moreno, Hector-
dc.contributor.authorReetz, Kathrin-
dc.contributor.authorThieme, Andreas-
dc.contributor.authorInfante, Jon-
dc.contributor.authorvan de Warrenburg, Bart P. C.-
dc.contributor.authorGiunti, Paola-
dc.contributor.authorRiess, Olaf-
dc.contributor.authorSchöls, Ludger-
dc.contributor.authorLima, Manuela-
dc.contributor.authorKlockgether, Thomas-
dc.contributor.authorJanuário, Cristina-
dc.contributor.authorAlmeida, Luís Pereira de-
dc.date.accessioned2024-02-20T12:22:06Z-
dc.date.available2024-02-20T12:22:06Z-
dc.date.issued2023-04-
dc.identifier.issn0305-1846pt
dc.identifier.issn1365-2990pt
dc.identifier.urihttps://hdl.handle.net/10316/113457-
dc.description.abstractThe European Spinocerebellar Ataxia Type 3/Machado-Joseph Disease Initiative (ESMI) is a consortium established with the ambition to set up the largest European longitudinal trial-ready cohort of Spinocerebellar Ataxia Type 3/Machado-Joseph Disease (SCA3/MJD), the most common autosomal dominantly inherited ataxia worldwide. A major focus of ESMI has been the identification of SCA3/MJD biomarkers to enable future interventional studies. As biosample collection and processing variables significantly impact the outcomes of biomarkers studies, biosampling procedures standardisation was done previously to study visit initiation. Here, we describe the ESMI consensus biosampling protocol, developed within the scope of ESMI, that ultimately might be translated to other neurodegenerative disorders, particularly ataxias, being the first step to protocol harmonisation in the field.pt
dc.language.isoengpt
dc.publisherWiley-Blackwellpt
dc.relationThis project was supported by the EU Joint Programme—Neurodegenerative Disease Research (JPND) through the following funding organisations under the aegis of JPND: Portugal, Foundation for Science and Technology (FCT, grant number JPCOFUND/0001/2015) and Regional Fund for Science and Technology of the Azores; Germany, Federal Ministry of Education and Research (BMBF; funding codes 01ED1602A/B); Netherlands, The Netherlands Organisation for Health Research and Development; United Kingdom, Medical Research Council. This project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement number 643417. In addition, support has been received by the ERDF through the Regional Operational Program Center 2020, Competitiveness Factors Operational Program (COMPETE 2020, POCI) and National Funds through FCT [BrainHealth2020 (CENTRO-01-0145-FEDER-000008), UID/NEU/04539/2019–2021, BDforMJD (CENTRO-01-0145-FEDER-181240), ViraVector (CENTRO- 01-0145-FEDER-022095), SpreadSilencing (POCI-01-0145- FEDER-029716)], and by the National Ataxia Foundation (USA), the American Portuguese Biomedical Research Fund (APBRF) and the Richard Chin and Lily Lock Machado-Joseph Disease Research Fund. MR (CEECIND/03018/2018), AFF (SFRH/BD/121101/2016), LG (PD/BD/135497/2018) and PS (SFRH/BD/148451/2019) are supported by FCT. PG is supported by the National Institute for Health Research University College London Hospitals Biomedical Research Centre UCLH. PG receives also support from the North Thames CRN. PG and HGM, work at University College London Hospitals/ University College London, which receives a proportion of funding from the Department of Health’s National Institute for Health Research Biomedical Research Centre’s funding scheme. PG received funding from CureSCA3 in support of HGM work.pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectataxiapt
dc.subjectbiomarkerspt
dc.subjectblood,pt
dc.subjectcerebrospinal fluidpt
dc.subjectneurodegenerative diseasespt
dc.subjectprotocolpt
dc.subjectresearchpt
dc.subjectstandardisationpt
dc.subject.meshHumanspt
dc.subject.meshBiomarkerspt
dc.subject.meshMachado-Joseph Diseasept
dc.subject.meshSpinocerebellar Ataxiaspt
dc.subject.meshCerebellar Ataxiapt
dc.subject.meshSpinocerebellar Degenerationspt
dc.titleA standardised protocol for blood and cerebrospinal fluid collection and processing for biomarker research in ataxiapt
dc.typearticle-
degois.publication.firstPagee12892pt
degois.publication.issue2pt
degois.publication.titleNeuropathology and Applied Neurobiologypt
dc.peerreviewedyespt
dc.identifier.doi10.1111/nan.12892pt
degois.publication.volume49pt
dc.date.embargo2023-04-01*
uc.date.periodoEmbargo0pt
item.openairetypearticle-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.fulltextCom Texto completo-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCIBB - Center for Innovative Biomedicine and Biotechnology-
crisitem.author.orcid0000-0001-9262-845X-
crisitem.author.orcid0000-0001-5402-3978-
crisitem.author.orcid0000-0001-5831-3307-
Appears in Collections:FFUC- Artigos em Revistas Internacionais
IIIUC - Artigos em Revistas Internacionais
I&D CIBB - Artigos em Revistas Internacionais
I&D CNC - Artigos em Revistas Internacionais
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