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Institution	Date	Title	Author
臺大學術典藏	2020-02-25T08:01:20Z	DCTN1 p.K56R in progressive supranuclear palsy	Gustavsson E.K;Trinh J;Guella I;Szu-Tu C;Khinda J;Lin C.-H;Ruey-Meei Wu;Stoessl J;Appel-Cresswell S;Mckeown M;Rajput A;Rajput A.H;Petersen M.S;Jeon B.S;Aasly J.O;Farrer M.J.; Gustavsson E.K; Trinh J; Guella I; Szu-Tu C; Khinda J; Lin C.-H; RUEY-MEEI WU; Stoessl J; Appel-Cresswell S; McKeown M; Rajput A; Rajput A.H; Petersen M.S; Jeon B.S; Aasly J.O; Farrer M.J.
臺大學術典藏	2020-02-25T08:01:20Z	Lovastatin protects neurite degeneration in LRRK2-G2019S parkinsonism through activating the Akt/Nrf pathway and inhibiting GSK3?] activity	Lin C.-H;Lin H.-I;Chen M.-L;Lai T.-T;Cao L.-P;Farrer M.J;Ruey-Meei Wu;Chien C.-T.; Lin C.-H; Lin H.-I; Chen M.-L; Lai T.-T; Cao L.-P; Farrer M.J; RUEY-MEEI WU; Chien C.-T.
臺大學術典藏	2020-02-25T08:01:20Z	Pathophysiology of small-fiber sensory system in Parkinson's disease: Skin innervation and contact heat evoked potential	Lin C.-H;Chao C.-C;Wu S.-W;Hsieh P.-C;Feng F.-P;Lin Y.-H;Chen Y.-M;Ruey-Meei Wu;Hsieh S.-T.; Lin C.-H; Chao C.-C; Wu S.-W; Hsieh P.-C; Feng F.-P; Lin Y.-H; Chen Y.-M; RUEY-MEEI WU; Hsieh S.-T.
臺大學術典藏	2020-02-25T08:01:19Z	Clinical heterogeneity of LRRK2 p.I2012T mutation	Fan T.-S;Ruey-Meei Wu;Chen P.-L;Chen T.-F;Li H.-Y;Lin Y.-H;Chen C.-Y;Chen M.-L;Tai C.-H;Lin H.-I;Lin C.-H.; Fan T.-S; RUEY-MEEI WU; Chen P.-L; Chen T.-F; Li H.-Y; Lin Y.-H; Chen C.-Y; Chen M.-L; Tai C.-H; Lin H.-I; Lin C.-H.
臺大學術典藏	2020-02-25T08:01:18Z	PINK1 Phosphorylates MIC60/Mitofilin to Control Structural Plasticity of Mitochondrial Crista Junctions	Tsai P.-I;Lin C.-H;Hsieh C.-H;Papakyrikos A.M;Kim M.J;Napolioni V;Schoor C;Couthouis J;Ruey-Meei Wu;Wszolek Z.K;Winter D;Greicius M.D;Ross O.A;Wang X.; Tsai P.-I; Lin C.-H; Hsieh C.-H; Papakyrikos A.M; Kim M.J; Napolioni V; Schoor C; Couthouis J; RUEY-MEEI WU; Wszolek Z.K; Winter D; Greicius M.D; Ross O.A; Wang X.
臺大學術典藏	2020-02-25T08:01:18Z	Lack of TMEM230 mutations in patients with familial and sporadic Parkinson's disease in a Taiwanese population	Fan T.-S;Lin C.-H;Lin H.-I;Chen M.-L;Ruey-Meei Wu; Fan T.-S; Lin C.-H; Lin H.-I; Chen M.-L; RUEY-MEEI WU
臺大學術典藏	2020-02-25T08:01:18Z	Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort	Lin H.-H;Ruey-Meei Wu;Lin H.-I;Chen M.-L;Tai C.-H;Lin C.-H.; Lin H.-H; RUEY-MEEI WU; Lin H.-I; Chen M.-L; Tai C.-H; Lin C.-H.
臺大學術典藏	2020-02-25T08:01:16Z	A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing	Lin C.-H;Chen P.-L;Tai C.-H;Lin H.-I;Chen C.-S;Chen M.-L;Ruey-Meei Wu; Lin C.-H; Chen P.-L; Tai C.-H; Lin H.-I; Chen C.-S; Chen M.-L; RUEY-MEEI WU
臺大學術典藏	2020-02-25T08:01:16Z	PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population	Fan T.-S;Ruey-Meei Wu;Lin H.-I;Cheng C;Lin C.-H.; Fan T.-S; RUEY-MEEI WU; Lin H.-I; Cheng C; Lin C.-H.
臺大學術典藏	2020-02-25T08:01:15Z	Genetic analysis of PODXL gene in patients with familial and young-onset Parkinson's disease in a Taiwanese population	Chen S.-J;Ruey-Meei Wu;Ho C.-H;Cheng J;Lin H.-Y;Lin C.-H.; Chen S.-J; RUEY-MEEI WU; Ho C.-H; Cheng J; Lin H.-Y; Lin C.-H.

Showing items 1586-1595 of 3227 (323 Page(s) Totally)
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