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  1. NTU Scholars
  2. Research Outputs

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0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing results 102 to 115 of 115 < previous 
Issue DateTitleAuthor(s)TypescopusWOSFulltext/Archive link
2001The COMT L allele modifies the association between MAOB polymorphism and PD in TaiwaneseRuey-Meei Wu journal article
2014The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease.Ruey-Meei Wu other
2014The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variantsRuey-Meei Wu ; Chin-Hsien Lin journal article208
2007The SCA17 phenotype can include features of MSA-C, PSP and cognitive impairmentRuey-Meei Wu journal article4539
2007Transcranial color-coded sonography helps differentiation between idiopathic Parkinson's disease and vascular parkinsonismRuey-Meei Wu ; JIANN-SHING JENG journal article5850
2007Transcranial imaging of substantia nigra hyperechogenicity in a Taiwanese cohort of Parkinson's diseaseRuey-Meei Wu ; JIANN-SHING JENG journal article7253
2012Unusual association of diseases/symptoms: Psychotic-affective symptoms and multiple system atrophy expand phenotypes of spinocerebellar ataxia type 2Ruey-Meei Wu ; KAI-HSIANG CHEN ; Chin-Hsien Lin journal article30
2014Vitamin D receptor genetic variants and Parkinson's disease in a Taiwanese populationRuey-Meei Wu ; KAI-HSIANG CHEN ; Chin-Hsien Lin journal article2019
2011VPS35 mutations in parkinson diseaseRuey-Meei Wu ; Vilariño-Güell, Carles; Wider, Christian; Ross, Owen A.; Dachsel, Justus C.; Kachergus, Jennifer M.; Lincoln, Sarah J.; Soto-Ortolaza, Alexandra I.; Cobb, Stephanie A.; Wilhoite, Greggory J.; Bacon, Justin A.; Behrouz, Bahareh; Melrose, Heather L.; Hentati, Emna; Puschmann, Andreas; Evans, Daniel M.journal article446427
2001多巴胺代謝酵素MAOB及COMT基因多型性與早發型巴金森氏病易感性之相關研究吳瑞美 journal article
1999氧化氮在MPTP神經毒理作用中所扮演的角色吳瑞美 journal article
2002行政院國家科學委員會專題研究計畫成果報告:COMT抑制劑entacapone對於巴金森氏病患者的血清catecholamine濃度及心臟血管系統的影響吳瑞美 journal article
2004行政院國家科學委員會專題研究計畫成果報告:台灣家族性及早發型(年輕型)巴金森氏病之臨床與基因研究(2/2)吳瑞美 journal article
2005行政院國家科學委員會專題研究計畫期中進度報告:Parkin 基因多型性與巴金森氏病致病感受性的關聯性、以及DJ-1基因變異在巴金森氏病扮演之角色(1/2)吳瑞美 journal article
Showing results 102 to 115 of 115 < previous 

關於(About)

臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

聯絡資訊(Contact Us)

總館學科館員(Main Library)
醫學圖書館學科館員(Medical Library)
社會科學院辜振甫紀念圖書館學科館員(Social Sciences Library)

相關網站(Useful Links)




關於開放取用(Open Access, OA)

開放取用是從使用者角度提升資訊取用性的社會運動,應用在學術研究上是透過將研究著作公開供使用者自由取閱,以促進學術傳播及因應期刊訂購費用逐年攀升。同時可加速研究發展、提升研究影研究影響力,NTU scholars即為本校的開放取用典藏(OA Archive)平台。(點選深入了解OA)

出版社期刊論文授權政策(Copyright)

  • 請確認所上傳的全文是原創的內容,若該文件包含部分內容的版權非匯入者所有,或由第三方贊助與合作完成,請確認該版權所有者及第三方同意提供此授權。Please represent that the submission is your original work, and that you have the right to grant the rights to upload.
  • 若欲上傳已出版的全文電子檔,可使用SHERPA RoMEO網站查詢,以確認出版單位之版權政策。Please useSHERPA RoMEO to find a summary of permissions that are normally given as part of each publisher's copyright transfer agreement.

使用說明(Instructions)

  • 網站簡介(Quickstart Guide)
  • 使用手冊(Instruction Manual)
  • 線上預約服務(Booking Service)

登入說明(Sign-in)

  • 方案一:臺灣大學計算機中心帳號登入
    (With C&INC Email Account)
  • 方案二:ORCID帳號登入(With ORCID)

匯入著作(Submission)

  • 方案一:定期更新ORCID者,以ID匯入(Search for identifier (ORCID))
  • 方案二:自行建檔(Default mode Submission)
  • 方案三:學科館員協助匯入(Email worklist to subject librarians)
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