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268th ENMC workshop - genetic diagnosis, clinical classification, outcome measures, and biomarkers in facioscapulohumeral muscular dystrophy (FSHD): relevance for clinical trials

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dc.contributor.coauthorMontagnese, Federica
dc.contributor.coauthorde Valle, Katy
dc.contributor.coauthorLemmers, Richard J.L.F.
dc.contributor.coauthorMul, Karlien
dc.contributor.coauthorDumonceaux, Julie
dc.contributor.coauthorVoermans, Nicol
dc.contributor.departmentSchool of Medicine
dc.contributor.facultymemberYes
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-12-29T09:39:09Z
dc.date.issued2023
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessN/A
dc.description.peerreviewstatusN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipThis work was supported by the FSHD Society, FSHD Global Research Foundation and European Neuromuscular Center (ENMC).
dc.description.studentonlypublicationNo
dc.description.studentpublicationNo
dc.description.versionN/A
dc.identifier.doi10.1016/j.nmd.2023.04.005
dc.identifier.eissn1873-2364
dc.identifier.embargoN/A
dc.identifier.endpage462
dc.identifier.issn0960-8966
dc.identifier.issue5
dc.identifier.link 
dc.identifier.pubmed37099914
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85153193795
dc.identifier.startpage447
dc.identifier.urihttps://doi.org/10.1016/j.nmd.2023.04.005
dc.identifier.urihttps://hdl.handle.net/20.500.14288/22908
dc.identifier.volume33
dc.identifier.wos000990105500001
dc.keywordsFacioscapulohumeral
dc.keywordsDystrophy
dc.keywordsENMC
dc.keywordsClinical trials
dc.language.isoeng
dc.publisherElsevier
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofNeuromuscular Disorders
dc.relation.openaccessN/A
dc.rightsN/A
dc.subjectClinical neurology
dc.subjectNeuromuscular disorders
dc.subjectNeurogenetics
dc.title268th ENMC workshop - genetic diagnosis, clinical classification, outcome measures, and biomarkers in facioscapulohumeral muscular dystrophy (FSHD): relevance for clinical trials
dc.typeOther
dspace.entity.typePublication
local.contributor.kuauthorOflazer, Piraye
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