Zur Kurzanzeige

dc.contributor.authorMorigaki, Ryoma
dc.contributor.authorNakataki, Masahito
dc.contributor.authorKawarai, Toshitaka
dc.contributor.authorLee, Lillian V.
dc.contributor.authorTeleg, Rosalia A.
dc.contributor.authorTabuena, Ma. Daisy P.
dc.contributor.authorMure, Hideo
dc.contributor.authorSako, Wataru
dc.contributor.authorPasco, Paul Matthew D.
dc.contributor.authorNagahiro, Shinji
dc.contributor.authorIga, Junichi
dc.contributor.authorOhmori, Tetsuro
dc.contributor.authorGoto, Satoshi
dc.contributor.authorKaji, Ryuji
dc.date.accessioned2024-05-03T03:45:40Z
dc.date.available2024-05-03T03:45:40Z
dc.date.issued2013-09-01
dc.identifier.citationMorigaki, R., Nakataki, M., Kawarai, T., Lee, L. V., Teleg, R. A., Tabuena, M. D., Mure, H., Sako, W., Pasco, P. M., Nagahiro, S., Iga, J., Ohmori, T., Goto, S., & Kaji, R. (2013). Depression in X-linked dystonia-parkinsonism: A case–control study. Parkinsonism & Related Disorders, 19(9), 844–846. https://doi.org/10.1016/j.parkreldis.2013.04.027en
dc.identifier.issn13538020
dc.identifier.urihttps://hdl.handle.net/20.500.14353/412
dc.description.abstractX-linked dystonia-parkinsonism (XDP), also known as lubag, was originally described as endemic to Panay, Philippines [ [1] ]. XDP demonstrates a primary and progressive neuronal degeneration of the striatum and is characterized by an adult-onset movement disorder that manifests as severe and progressive dystonia with a high frequency of generalization, followed by the onset of a parkinsonian state in the later years of life [ 1 , 2 ]. Suicide incidence has been reported to account for 9% of the mortality in patients with XDP [ [1] ]. Despite the high suicide risk, only a few case reports refer to mood disorders in patients with XDP. The purpose of this study was to determine the prevalence of depressive symptoms among patients with XDP.en
dc.description.sponsorshipThis work was supported by grants from the Ministry of Educa- tion, Culture, Sports, Science and Technology of Japan (grant-in-aid for Scientific Research, 23500428, 24390223).
dc.language.isoenen
dc.publisherElsevier Inc.en
dc.subjectDepressive disorderen
dc.subjectDystonic disordersen
dc.subjectHeredodegenerative disordersen
dc.subjectNervous Systemen
dc.subjectParkinsonian disordersen
dc.subjectDystonia 3, Torsion, X-linkeden
dc.subjectNeuronal degenerationen
dc.subjectMood disorderen
dc.subjectHigh suicide risken
dc.subjectDepressive symptomsen
dc.subject.lcshX-linked mental retardationen
dc.subject.lcshParkinson's diseaseen
dc.subject.lcshGenetic disordersen
dc.subject.lcshDystoniaen
dc.subject.lcshDepressionsen
dc.subject.meshParkinson Diseaseen
dc.subject.meshDystonic Disordersen
dc.subject.meshGenetic Diseases, X-Linkeden
dc.subject.meshCase-Control Studiesen
dc.subject.meshDepressionen
dc.subject.meshDystonic Disordersen
dc.subject.meshHeredodegenerative Disorders, Nervous Systemen
dc.subject.meshHumansen
dc.subject.meshMaleen
dc.titleDepression in X-linked dystonia-parkinsonism: A case-control studyen
dc.typeArticleen
dcterms.accessRightsLimited public accessen
dc.citation.journaltitleParkinsonism and Related Disordersen
dc.citation.volume19en
dc.citation.issue9en
dc.citation.firstpage844en
dc.citation.lastpage846en
dc.identifier.doi10.1016/j.parkreldis.2013.04.027
local.isIndexedByScopusen


Dateien zu dieser Ressource

Thumbnail

Das Dokument erscheint in:

Zur Kurzanzeige