第 1 到 12 筆結果,共 12 筆。
公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 | |
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1 | 2019 | Using global team science to identify genetic parkinson's disease worldwide | Vollstedt E.-J.; Kasten M.; Klein C.; Aasly J.; Adler C.; Ahmad-Annuar A.; Albanese A.; Alcalay R.N.; Al-Mubarak B.; Alvarez V.; Andree-Mu?oz B.; Annesi G.; Appel-Cresswell S.; Arkadir D.; Armasu S.; Barber T.R.; Bardien S.; Barkhuizen M.; Barrett M.J.; Ba?ak A.N.; Beach T.; Benitez B.A.; Berg D.; Bhatia K.; Binkofski F.; Blauwendraat C.; Bonifati V.; Borges V.; Bozi M.; Brice A.; Brighina L.; Brockmann K.; Br?cke T.; Br?ggemann N.; Camacho M.; Cardoso F.; Belin A.C.; Carr J.; Chan P.; Chang-Castello J.; Chase B.; Chen-Plotkin A.; Ju Chung S.; Cilia R.; Clarimon J.; Clark L.; Cornejo-Olivas M.; Corvol J.-C.; Cosentino C.; Cras P.; Crosiers D.; Dam?sio J.; Das P.; de Carvalho Aguiar P.; De Michele G.; De Rosa A.; Dieguez E.; Dorszewska J.; Erer S.; Ertan S.; Farrer M.; Fedotova E.; Ferese R.; Ferrarese C.; Ferraz H.; Fiala O.; Foroud T.; Friedman A.; Frigerio R.; Funayama M.; Gambardella S.; Garraux G.; Gatto E.M.; Gen? G.; Giladi N.; Goldwurm S.; Gomez-Esteban J.C.; G?mez-Garre P.; Gorostidi A.; Grosset D.; Hanagasi H.; Hardy J.; Hassan A.; Hattori N.; Hauser R.A.; Hedera P.; Hentati F.; Hertz J.M.; Holton J.L.; Houlden H.; Hutz M.H.; Ikeuchi T.; Illarioshkin S.; Inca-Martinez M.; Infante J.; Jankovic J.; Jeon B.S.; Jes?s S.; Jimenez-Del-Rio M.; Kaasinen V.; Kasten M.; Kataoka H.; Kawakami H.; Kim Y.J.; Klein C.; Kliv?nyi P.; Koks S.; K?nig I.R.; Kosti? V.; Koziorowski D.; Kr?ger R.; Krygowska-Wajs A.; Kulisevsky J.; Lai D.; Lang A.; LeDoux M.; Lesage S.; Lim S.-Y.; CHIN-HSIEN LIN ; Lohmann K.; Lopera F.; Lopez G.; Lu C.-S.; Lynch T.; Machaczka M.; Madoev H.; Magalh?es M.; Majamaa K.; Maraganore D.; Marder K.; Markopoulou K.; Martikainen M.H.; Mata I.; Mazzetti P.; Mellick G.; Men?ndez-Gonz?lez M.; Micheli F.; Mirelman A.; Mir P.; Morino H.; Morris H.; Munhoz R.P.; Naito A.; Olszewska D.A.; Ozelius L.J.; Padmanabhan S.; Pais?n-Ruiz C.; Payami H.; Peluso S.; Petkovic S.; Petrucci S.; Pezzoli G.; Pimentel M.; Pirker W.; Pramstaller P.P.; Pulkes T.; Puschmann A.; Quattrone A.; Raggio V.; Ransmayr G.; Rieder C.; Riess O.; Rodriguez-Porcel F.; Rogaeva E.; Ross O.A.; Ruiz-Martinez J.; Sammler E.; San Luciano M.; Satake W.; Saunders-Pullman R.; Sazci A.; Scherzer C.; Schrag A.; Schumacher-Schuh A.; Sharma M.; Sidransky E.; Singleton A.B.; Petersen M.S.; Smolders S.; Spitz M.; Stefanis L.; Struhal W.; Sue C.M.; Swan M.; Swanberg M.; Taba P.; Taipa R.; Tan M.; Tan A.H.; Tan E.-K.; Tang B.; Tayebi N.; Thaler A.; Thomas A.; Toda T.; Toft M.; Torres L.; Tumas V.; Valente E.M.; Van Broeckhoven C.; Vecsei L.; Velez-Pardo C.; Vidailhet M.; Vollstedt E.-J.; Warner T.T.; Williams-Gray C.H.; Winkelmann J.; Woitalla D.; Wood N.W.; Wszolek Z.K.; RUEY-MEEI WU ; Wu Y.-R.; Xie T.; Yoshino H.; Zhang B.; Zimprich A.; MJFF Global Genetic Parkinson's Disease Study Group | Annals of Neurology | 22 | 24 | |
2 | 2021 | Updates on the genetics of parkinson’s disease: Clinical implications and future treatment | Chu, Yung-Tsai; CHUN-HWEI TAI ; CHIN-HSIEN LIN ; RUEY-MEEI WU | Acta Neurologica Taiwanica | 9 | 0 | |
3 | 2021 | Reply: UQCRC1 variants in Parkinson's disease: a large cohort study in Chinese mainland population | CHIN-HSIEN LIN ; Farrer M.J.; RUEY-MEEI WU | Brain : a journal of neurology | 0 | 1 | |
4 | 2014 | The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease. | RUEY-MEEI WU ; CHIN-HSIEN LIN ; Lin H.I. | Neurology | 13 | 12 | |
5 | 2013 | Mystery Case: Hemiballism in a patient with parietal lobe infarction | MENG-CHEN WU ; RUOH-FANG YEN ; CHIN-HSIEN LIN ; RUEY-MEEI WU ; Nita D.A. | Neurology | 3 | 2 | |
6 | 2020 | Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy | CHIN-HSIEN LIN ; Tsai, Pei-I; Lin, Han-Yi; Hattori, Nobutaka; Funayama, Manabu; Jeon, Beomseok; Sato, Kota; Abe, Koji; Mukai, Yohei; Takahashi, Yuji; Li, Yuanzhe; Nishioka, Kenya; Yoshino, Hiroyo; Daida, Kensuke; Chen, Meng-Ling; Cheng, Jay; Huang, Cheng-Yen; SHIOU-RU TZENG ; Wu, Yen-Sheng; Lai, Hsing-Jung; Tsai, Hsin-Hsi; RUOH-FANG YEN ; NI-CHUNG LEE ; Lo, Wen-Chun; Hung, Yu-Chien; CHIH-CHIANG CHAN ; Ke, Yi-Ci; CHI-CHAO CHAO ; SUNG-TSANG HSIEH ; Farrer, Matthew; RUEY-MEEI WU | Brain : a journal of neurology | 29 | 32 | |
7 | 2011 | LRRK2 Parkinson's disease: From animal models to cellular mechanisms | CHIN-HSIEN LIN ; Tsai P.-I.; RUEY-MEEI WU ; Chin C.-T. | Reviews in the Neurosciences | 10 | 11 | |
8 | 2009 | Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation | CHUN-HWEI TAI ; RUOH-FANG YEN ; CHIN-HSIEN LIN ; Yen K.-Y.; Yip P.-K.; RUEY-MEEI WU ; MING-JEN LEE | Parkinsonism and Related Disorders | 3 | 2 | |
9 | 2021 | Erratum to: Reply: UQCRC1 variants in Parkinson's disease: a large cohort study in Chinese mainland population | CHIN-HSIEN LIN ; Farrer, Matthew J; RUEY-MEEI WU | Brain : a journal of neurology | 0 | 0 | |
10 | 2012 | Early-onset autosomal-recessive parkinsonian-pyramidal syndrome | Lai H.-J; CHIN-HSIEN LIN ; RUEY-MEEI WU | Acta Neurologica Taiwanica | 9 | 0 | |
11 | 2015 | COQ2 gene variants associate with cerebellar subtype of multiple system atrophy in Chinese | CHIN-HSIEN LIN ; Tan E.-K.; Yang C.-C.; Yi Z.; RUEY-MEEI WU | Movement Disorders | 33 | 31 | |
12 | 2015 | Biomarkers of cognitive decline in Parkinson's disease | CHIN-HSIEN LIN ; RUEY-MEEI WU | Parkinsonism and Related Disorders | 77 | 72 |