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Frequency of non-motor symptoms in Parkinson's disease patients carrying the E326K and T369M GBA risk variants

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dc.contributor.coauthorUsnich, Tatiana
dc.contributor.coauthorOlmedillas, Maria
dc.contributor.coauthorSchell, Nathalie
dc.contributor.coauthorPaul, Jefri J.
dc.contributor.coauthorCurado, Filipa
dc.contributor.coauthorSkobalj, Snezana
dc.contributor.coauthorCsoti, Ilona
dc.contributor.coauthorGruber, Doreen
dc.contributor.coauthorZittel, Simone
dc.contributor.coauthorSammler, Esther
dc.contributor.coauthorIsaacson, Stuart H.
dc.contributor.coauthorKühn, Andrea A.
dc.contributor.coauthorPedrosa, David J.
dc.contributor.coauthorReetz, Kathrin
dc.contributor.coauthorKasten, Meike
dc.contributor.coauthorRolfs, Arndt
dc.contributor.coauthorBauer, Peter
dc.contributor.coauthorSkrahina, Volha
dc.contributor.coauthorKlein, Christine
dc.contributor.coauthorBrüggemann, Norbert
dc.contributor.kuauthorErtan, Fatoş Sibel
dc.contributor.kuprofileFaculty Member
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.yokid112829
dc.date.accessioned2024-11-09T23:52:51Z
dc.date.issued2023
dc.description.abstractN/A
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.indexedbyWoS
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.volume107
dc.identifier.doi10.1016/j.parkreldis.2022.105248
dc.identifier.issn1353-8020
dc.identifier.linkhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85144832842&doi=10.1016%2fj.parkreldis.2022.105248&partnerID=40&md5=e7d7be5003e4f0f64c9768cb059ad334
dc.identifier.scopus2-s2.0-85144832842
dc.identifier.urihttp://dx.doi.org/10.1016/j.parkreldis.2022.105248
dc.identifier.urihttps://hdl.handle.net/20.500.14288/14919
dc.identifier.wos956444500001
dc.keywordsGBA risk variants
dc.keywordsNon-motor symptoms
dc.keywordsParkinson's disease genetic predisposition to disease
dc.keywordsGenotype
dc.keywordsGlucosylceramidase
dc.keywordsHumans
dc.keywordsMutation
dc.keywordsParkinson disease
dc.keywordsGlucosylceramidase
dc.keywordsLeucine rich repeat kinase 2
dc.keywordsAdult
dc.keywordsBrief smell identification test
dc.keywordsCognition
dc.keywordsControlled study
dc.keywordsDisease duration
dc.keywordsDisease exacerbation
dc.keywordsDisease severity assessment
dc.keywordsE326K gene
dc.keywordsEpworth sleepiness scale
dc.keywordsEvaluation and follow up
dc.keywordsExploratory behavior
dc.keywordsFemale
dc.keywordsGaucher disease
dc.keywordsGene frequency
dc.keywordsGene sequence
dc.keywordsGenetic analysis
dc.keywordsGenetic risk
dc.keywordsGenetic screening
dc.keywordsHallucination
dc.keywordsHeterozygous
dc.keywordsHigh throughput sequencing
dc.keywordsHospital anxiety and depression scale
dc.keywordsHuman
dc.keywordsHyposmia
dc.keywordsInsomnia
dc.keywordsLetter
dc.keywordsLogistic regression analysis
dc.keywordsMale
dc.keywordsMontreal cognitive assessment
dc.keywordsMood alteration
dc.keywordsMotor activity
dc.keywordsMovement Disorder Society Unified Parkinsons Disease Rating Scale
dc.keywordsMultivariate logistic regression analysis
dc.keywordsNeuromodulation
dc.keywordsNon motor symptom
dc.keywordsOnset age
dc.keywordsParkinson disease
dc.keywordsPhenotype
dc.keywordsPittsburgh Sleep Quality Inventory
dc.keywordsRisk factor
dc.keywordsRisk variant
dc.keywordsScales for outcomes in Parkinsons disease autonomic symptom
dc.keywordsSequence analysis
dc.keywordsSymptom assessment
dc.keywordsT369M gene
dc.keywordsUnified Parkinson disease rating scale
dc.keywordsComplication
dc.keywordsGenetic predisposition
dc.keywordsGenetics
dc.keywordsGenotype
dc.keywordsMutation
dc.languageEnglish
dc.publisherElsevier Ltd
dc.sourceParkinsonism and Related Disorders
dc.subjectMedicine
dc.titleFrequency of non-motor symptoms in Parkinson's disease patients carrying the E326K and T369M GBA risk variants
dc.typeLetter
dspace.entity.typePublication
local.contributor.authorid0000-0003-1339-243X
local.contributor.kuauthorErtan, Fatoş Sibel

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