Show simple item record

dc.contributor.authorRietveld, A.
dc.contributor.authorMassaro, F.
dc.contributor.authorFederico, A.
dc.contributor.authorTaglia, I.
dc.contributor.authorBattisti, C.
dc.contributor.authorMarconi, R.
dc.contributor.authorOnofrj, M.
dc.contributor.authorThomas, A.
dc.contributor.authorVanacore, N.
dc.contributor.authorMeco, G.
dc.contributor.authorFabbrini, G.
dc.contributor.authorFabrizio, E.
dc.contributor.authorBerardelli, A.
dc.contributor.authorStocchi, F.
dc.contributor.authorVacca, L.
dc.contributor.authorPicillo, M.
dc.contributor.authorDe Rosa, A.
dc.contributor.authorCriscuolo, C.
dc.contributor.authorDe Michele, G.
dc.contributor.authorFilla, A.
dc.contributor.authorBarone, P.
dc.contributor.authorDe Mari, M.
dc.contributor.authorDell'Aquila, C.
dc.contributor.authorIliceto, G.
dc.contributor.authorLamberti, P.
dc.contributor.authorToni, V.
dc.contributor.authorTrianni, G.
dc.contributor.authorGagliardi, M.
dc.contributor.authorAnnesi, G.
dc.contributor.authorQuattrone, A.
dc.contributor.authorCossu, G.
dc.contributor.authorMelis, M.
dc.contributor.authorTufekcioglu, Z.
dc.contributor.authorBilgic, B.
dc.contributor.authorHanagasi, Haşmet Ayhan
dc.contributor.authorSaddi, V.
dc.contributor.authorLopiano, L.
dc.contributor.authorOlgiati, Simone
dc.contributor.authorQuadri, Marialuisa
dc.contributor.authorFang, Mingyan
dc.contributor.authorRood, Janneke P. M. A.
dc.contributor.authorSaute, Jonas A.
dc.contributor.authorChien, Hsin Fen
dc.contributor.authorBouwkamp, Christian G.
dc.contributor.authorGraafland, Josja
dc.contributor.authorMinneboo, Michelle
dc.contributor.authorBreedveld, Guido J.
dc.contributor.authorZhang, Jianguo
dc.contributor.authorVerheijen, Frans W.
dc.contributor.authorBoon, Agnita J. W.
dc.contributor.authorKievit, Anneke J. A.
dc.contributor.authorJardim, Laura Bannach
dc.contributor.authorMandemakers, Wim
dc.contributor.authorBarbosa, Egberto Reis
dc.contributor.authorRieder, Carlos R. M.
dc.contributor.authorLeenders, Klaus L.
dc.contributor.authorWang, Jun
dc.contributor.authorBonifati, Vincenzo
dc.contributor.authorvan de Warrenburg, B.
dc.contributor.authorDelnooz, C.
dc.contributor.authorBloem, B.
dc.contributor.authorFerreira, J.
dc.contributor.authorCorreia Guedes, L.
dc.contributor.authorTolosa, E.
dc.contributor.authorKurtiz, M. M.
dc.contributor.authorObeso, J.
dc.contributor.authorEmre, M.
dc.contributor.authorElibol, B.
dc.contributor.authorLu, Chin-Song
dc.contributor.authorWu-Chou, Yah-Huei
dc.contributor.authorYeh, Tu-Hsueh
dc.contributor.authorAtadzhanov, M.
dc.contributor.authorKelly, P.
dc.contributor.authorTassorelli, C.
dc.contributor.authorPacchetti, C.
dc.contributor.authorNappi, G.
dc.contributor.authorRiboldazzi, G.
dc.contributor.authorBono, G.
dc.contributor.authorComi, C.
dc.contributor.authorPadovani, A.
dc.contributor.authorBorroni, B.
dc.contributor.authorRaudino, F.
dc.contributor.authorFincati, E.
dc.contributor.authorBertolasi, L.
dc.contributor.authorTinazzi, M.
dc.contributor.authorBonizzato, A.
dc.contributor.authorFerracci, C.
dc.contributor.authorLibera, A. Dalla
dc.contributor.authorMarini, P.
dc.date.accessioned2021-03-06T11:17:45Z
dc.date.available2021-03-06T11:17:45Z
dc.date.issued2016
dc.identifier.citationOlgiati S., Quadri M., Fang M., Rood J. P. M. A. , Saute J. A. , Chien H. F. , Bouwkamp C. G. , Graafland J., Minneboo M., Breedveld G. J. , et al., "DNAJC6 Mutations Associated With Early-Onset Parkinson's Disease", ANNALS OF NEUROLOGY, cilt.79, ss.244-256, 2016
dc.identifier.issn0364-5134
dc.identifier.othervv_1032021
dc.identifier.otherav_ee573f83-06c2-4220-bd5b-f0f28ec7e6f5
dc.identifier.urihttp://hdl.handle.net/20.500.12627/156462
dc.identifier.urihttps://doi.org/10.1002/ana.24553
dc.description.abstractObjectiveDNAJC6 mutations were recently described in two families with autosomal recessive juvenile parkinsonism (onset age<11), prominent atypical signs, poor or absent response to levodopa, and rapid progression (wheelchair-bound within approximate to 10 years from onset). Here, for the first time, we report DNAJC6 mutations in early-onset Parkinson's disease (PD).
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectNEUROSCIENCES
dc.subjectSinirbilim ve Davranış
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleDNAJC6 Mutations Associated With Early-Onset Parkinson's Disease
dc.typeMakale
dc.relation.journalANNALS OF NEUROLOGY
dc.contributor.departmentS Francesco Hosp , ,
dc.identifier.volume79
dc.identifier.issue2
dc.identifier.startpage244
dc.identifier.endpage256
dc.contributor.firstauthorID230316


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record