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機構 日期 題名 作者
臺大學術典藏 2020-02-25T08:01:44Z Selegiline (l-deprenyl) as a unique neuroprotective agent for chronic neurodegenerative disorders - A lesson from MAO inhibition Ruey-Meei Wu;Murphy D.L;Chiueh C.C.; RUEY-MEEI WU; Murphy D.L; Chiueh C.C.
臺大學術典藏 2020-02-25T08:01:43Z Acute disseminated encephalomyelitis: A follow-up study in Taiwan Lin C.-H;Jeng J.-S;Hsieh S.-T;Yip P.-K;Ruey-Meei Wu; Lin C.-H; Jeng J.-S; Hsieh S.-T; Yip P.-K; RUEY-MEEI WU
臺大學術典藏 2020-02-25T08:01:43Z The SCA17 phenotype can include features of MSA-C, PSP and cognitive impairment Lin I.-S;Ruey-Meei Wu;Lee-Chen G.-J;Shan D.-E;Gwinn-Hardy K.; Lin I.-S; RUEY-MEEI WU; Lee-Chen G.-J; Shan D.-E; Gwinn-Hardy K.
臺大學術典藏 2020-02-25T08:01:43Z Transcranial color-coded sonography helps differentiation between idiopathic Parkinson's disease and vascular parkinsonism Tsai C.-F;Ruey-Meei Wu;Huang Y.-W;Chen L.-L;Yip P.-K;Jeng J.-S.; Tsai C.-F; RUEY-MEEI WU; Huang Y.-W; Chen L.-L; Yip P.-K; Jeng J.-S.
臺大學術典藏 2020-02-25T08:01:43Z Transcranial imaging of substantia nigra hyperechogenicity in a Taiwanese cohort of Parkinson's disease Huang Y.-W;Jeng J.-S;Tsai C.-F;Chen L.-L;Ruey-Meei Wu; Huang Y.-W; Jeng J.-S; Tsai C.-F; Chen L.-L; RUEY-MEEI WU
臺大學術典藏 2020-02-25T08:01:43Z Pesticide exposure on southwestern Taiwanese with MnSOD and NQO1 polymorphisms is associated with increased risk of Parkinson's disease Fong C.-S;Ruey-Meei Wu;Shieh J.-C;Chao Y.-T;Fu Y.-P;Kuao C.-L;Cheng C.-W.; Fong C.-S; RUEY-MEEI WU; Shieh J.-C; Chao Y.-T; Fu Y.-P; Kuao C.-L; Cheng C.-W.
臺大學術典藏 2020-02-25T08:01:43Z Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia Farrer M.J; Stone J.T; Lin C.-H; D?chsel J.C; Hulihan M.M; Haugarvoll K; Ross O.A; RUEY-MEEI WU
臺大學術典藏 2020-02-25T08:01:42Z Lrrk2 R1628P in non-Chinese Asian races Tan E.-K; Tang M; Tan L.C; Wu Y.-R; RUEY-MEEI WU; Ross O.A; Zhao Y.
臺大學術典藏 2020-02-25T08:01:42Z Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore Lin C.H; Tan E.K; Chen M.L; Tan L.C; Lim H.Q; Chen G.S; RUEY-MEEI WU
臺大學術典藏 2020-02-25T08:01:42Z LRRK2 mutation in familial Parkinson's disease in a Taiwanese population: Clinical, PET, and functional studies Lin C.-H; Tzen K.-Y; Yu C.-Y; Tai C.-H; Farrer M.J; RUEY-MEEI WU

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