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Performance of the 12-item WHODAS 2.0 in prodromal Huntington disease

dc.contributor.authorKim, Ji-In
dc.contributor.authorLong, Jeffrey D
dc.contributor.authorMills, James A
dc.contributor.authorDowning, Nancy
dc.contributor.authorWilliams, Janet K
dc.contributor.authorPaulsen, Jane S
dc.contributor.authorPREDICT-HD Investigators And Coordinators Of The Huntington Study Group
dc.contributor.authorMiedzybrodzka, Zofia Helena
dc.date.accessioned2015-10-20T10:20:01Z
dc.date.available2015-10-20T10:20:01Z
dc.date.issued2015
dc.identifier57877310
dc.identifierf138c6a2-4dbb-4924-b60d-dab0b5f92f18
dc.identifier25735480
dc.identifier84944352913
dc.identifier.citationKim , J-I , Long , J D , Mills , J A , Downing , N , Williams , J K , Paulsen , J S , PREDICT-HD Investigators And Coordinators Of The Huntington Study Group & Miedzybrodzka , Z H 2015 , ' Performance of the 12-item WHODAS 2.0 in prodromal Huntington disease ' , EJHG : European journal of human genetics : the official journal of the European Society of Human Genetics. , vol. 23 , no. 11 , pp. 1584-1587 . https://doi.org/10.1038/ejhg.2015.11en
dc.identifier.issn1018-4813
dc.identifier.urihttp://hdl.handle.net/2164/5084
dc.descriptionACKNOWLEDGEMENTS We thank the PREDICT-HD sites, the study participants, the National Research Roster for Huntington Disease Patients and Families, the Huntington’s Disease Society of America and the Huntington Study Group. This publication was supported by the National Center for Advancing Translational Sciences, and the National Institutes of Health (NIH), through Grant 2 UL1 TR000442-06. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH. This research is supported by the National Institutes of Health, National Institute of Neurological Disorders and Stroke (5R01NS040068) awarded to Dr Paulsen, CHDI Foundation, Inc (A3917) awarded to Dr Paulsen, Cognitive and Functional Brain Changes in Preclinical Huntington’s Disease (HD) (5R01NS054893) awarded to Dr Paulsen, 4D Shape Analysis for Modeling Spatiotemporal Change Trajectories in Huntington’s (1U01NS082086), Functional Connectivity in Premanifest Huntington’s Disease (1U01NS082083), and Basal Ganglia Shape Analysis and Circuitry in Huntington’s Disease (1U01NS082085).en
dc.format.extent4
dc.format.extent1492034
dc.language.isoeng
dc.relation.ispartofEJHG : European journal of human genetics : the official journal of the European Society of Human Genetics.en
dc.subjectQH426 Geneticsen
dc.subject.lccQH426en
dc.titlePerformance of the 12-item WHODAS 2.0 in prodromal Huntington diseaseen
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen.Applied Medicineen
dc.contributor.institutionUniversity of Aberdeen.Grampian Data Safe Haven (DaSH)en
dc.contributor.institutionUniversity of Aberdeen.Institute of Medical Sciencesen
dc.description.statusPeer revieweden
dc.identifier.doi10.1038/ejhg.2015.11


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