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"ruey meei wu"的相關文件
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| 臺大學術典藏 |
2018-09-10T08:31:10Z |
VPS35 mutations in parkinson disease
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吳瑞美; Vilariño-Güell, C. and Wider, C. and Ross, O.A. and Dachsel, J.C. and Kachergus, J.M. and Lincoln, S.J. and Soto-Ortolaza, A.I. and Cobb, S.A. and Wilhoite, G.J. and Bacon, J.A. and Bahareh Behrouz, and Melrose, H.L. and Hentati, E. and Puschmann, A. and Evans, D.M. and Conibear, E. and Wasserman, W.W. and Aasly, J.O. and Burkhard, P.R. and Djaldetti, R. and Ghika, J. and Hentati, F. and Krygowska-Wajs, A. and Lynch, T. and Melamed, E. and Rajput, A. and Rajput, A.H. and Solida, A. and Wu, R.-M. and Uitti, R.J. and Wszolek, Z.K. and Vingerhoets, F. and Farrer, M.J.; Evans, Daniel?M.; Puschmann, Andreas; Hentati, Emna; Melrose, Heather?L.; 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.; Ruey-Meei Wu; Vilari?o-G?ell, 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 |
| 臺大學術典藏 |
2018-09-10T08:31:09Z |
Death-associated protein kinase 1 variation and Parkinson's disease
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Dachsel, J.C. and Wider, C. and Vilariño-Güell, C. and Aasly, J.O. and Rajput, A. and Rajput, A.H. and Lynch, T. and Craig, D. and Krygowska-Wajs, A. and Jasinska-Myga, B. and Opala, G. and Barcikowska, M. and Czyzewski, K. and Wu, R..-M. and Heckman, M.G. and Uitti, R.J. and Wszolek, Z.K. and Farrer, M.J. and Ross, O.A.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T08:31:09Z |
Erratum: VPS35 mutations in Parkinson disease (American Journal of Human Genetics (2011) 89 (162-167))
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Vilariño-Güell, C. and Wider, C. and Ross, O.A. and Dachsel, J.C. and Kachergus, J.M. and Lincoln, S.J. and Soto-Ortolaza, A.I. and Cobb, S.A. and Wilhoite, G.J. and Bacon, J.A. and Behrouz, B. and Melrose, H.L. and Hentati, E. and Puschmann, A. and Evans, D.M. and Conibear, E. and Wasserman, W.W. and Aasly, J.O. and Burkhard, P.R. and Djaldetti, R. and Ghika, J. and Hentati, F. and Krygowska-Wajs, A. and Lynch, T. and Melamed, E. and Rajput, A. and Rajput, A.H. and Solida, A. and Wu, R.-M. and Uitti, R.J. and Wszolek, Z.K. and Vingerhoets, F. and Farrer, M.J.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T08:31:09Z |
LRRK2 Parkinson's disease: From animal models to cellular mechanisms
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Lin, C.-H. and Tsai, P.-I. and Wu, R.-M. and Chin, C.-T.; Ruey-Meei Wu; Chin-Hsien Lin |
| 臺大學術典藏 |
2018-09-10T08:31:09Z |
Lrrk2 S1647T and BDNF V66M interact with environmental factors to increase risk of Parkinson's disease
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Lin, C.-H. and Wu, R.-M. and Tai, C.-H. and Chen, M.-L. and Hu, F.-C.; Ruey-Meei Wu; CHUN-HWEI TAI; Chin-Hsien Lin |
| 臺大學術典藏 |
2018-09-10T08:31:08Z |
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: A case-control study
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Ross, O.A. and Soto-Ortolaza, A.I. and Heckman, M.G. and Aasly, J.O. and Abahuni, N. and Annesi, G. and Bacon, J.A. and Bardien, S. and Bozi, M. and Brice, A. and Brighina, L. and Van Broeckhoven, C. and Carr, J. and Chartier-Harlin, M.-C. and Dardiotis, E. and Dickson, D.W. and Diehl, N.N. and Elbaz, A. and Ferrarese, C. and Ferraris, A. and Fiske, B. and Gibson, J.M. and Gibson, R. and Hadjigeorgiou, G.M. and Hattori, N. and Ioannidis, J.P.A. and Jasinska-Myga, B. and Jeon, B.S. and Kim, Y.J. and Klein, C. and Kruger, R. and Kyratzi, E. and Lesage, S. and Lin, C.-H. and Lynch, T. and Maraganore, D.M. and Mellick, G.D. and Mutez, E. and Nilsson, C. and Opala, G. and Park, S.S. and Puschmann, A. and Quattrone, A. and Sharma, M. and Silburn, P.A. and Sohn, Y.H. and Stefanis, L. and Tadic, V. and Theuns, J. and Tomiyama, H. and Uitti, R.J. and Valente, E.M. and van de Loo, S. and Vassilatis, D.K. and Vilariño-Güell, C. and White, L.R. and Wirdefeldt, K. and Wszolek, Z.K. and Wu, R.-M. and Farrer, M.J.; Ruey-Meei Wu; Chin-Hsien Lin |
| 臺大學術典藏 |
2018-09-10T08:31:08Z |
Author response
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Yen, C.-Y. and Lin, K.-H. and Hu, M.-H. and Wu, R.-M. and Lu, T.-W. and Lin, C.-H.; Ruey-Meei Wu; MING-HSIA HU |
| 臺大學術典藏 |
2018-09-10T08:30:42Z |
Meige syndrome relieved by bilateral pallidal stimulation with cycling mode: Case report
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Tai, C.-H. and Wu, R.-M. and Liu, H.-M. and Tsai, C.-W. and Tseng, S.-H.; CHUN-HWEI TAI; Ruey-Meei Wu; HON-MAN LIU |
| 臺大學術典藏 |
2018-09-10T08:06:36Z |
O6-Methylguanine-DNA methyltransferase expression and prognostic value in brain metastases of lung cancers
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Wu, Pei-Fang;Kuo, Kuan-Ting;Kuo, Lu-Ting;Lin, Yi-Ting;Lee, Wei-Chung;Lu, Yen-Shen;Yang, Chih-Hsin;Wu, Ruey-Meei;Tu, Yong-Kwang;Tasi, Jui-Chang;Tseng, Ham-Min;Tseng, Sheng-Hong;Cheng, Ann-Lii;Lin, Ching-Hung; Wu, Pei-Fang; Ruey-Meei Wu; Lu-Ting Kuo; Kuo, Kuan-Ting; Kuo, Lu-Ting; Yong-Kwang Tu; Lin, Yi-Ting; CHING-HUNG LIN; KUAN-TING KUO; Lee, Wei-Chung; ANN-LII CHENG; Lu, Yen-Shen; Yang, Chih-Hsin; Wu, Ruey-Meei; Tu, Yong-Kwang; Tasi, Jui-Chang; Tseng, Ham-Min; Tseng, Sheng-Hong; Cheng, Ann-Lii; Lin, Ching-Hung |
| 臺大學術典藏 |
2018-09-10T08:05:07Z |
Rapid screening of ATP13A2 variant with highresolution melting analysis
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Funayama, M. and Tomiyama, H. and Wu, R.-M. and Ogaki, K. and Yoshino, H. and Mizuno, Y. and Hattori, N.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T08:05:06Z |
LRRK2 G2019S mutation induces dendrite degeneration through mislocalization and phosphorylation of tau by recruiting autoactivated GSK3β
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Lin, C.-H. and Tsai, P.-I. and Wu, R.-M. and Chien, C.-T.; Ruey-Meei Wu; Chin-Hsien Lin |
| 臺大學術典藏 |
2018-09-10T08:05:06Z |
Multiple LRRK2 variants modulate risk of Parkinson disease: A Chinese multicenter study
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Tan, E.-K. and Peng, R. and Teo, Y.-Y. and Tan, L.C. and Angeles, D. and Ho, P. and Chen, M.-L. and Lin, C.-H. and Mao, X.-Y. and Chang, X.-L. and Prakash, K.M. and Liu, J.-J. and Au, W.-L. and Le, W.-D. and Jankovic, J. and Burgunder, J.-M. and Zhao, Y. and Wu, R.-M.; Ruey-Meei Wu; Chin-Hsien Lin |
| 臺大學術典藏 |
2018-09-10T08:05:06Z |
Feeling-of-knowing in episodic memory in patients with Parkinson's disease with various motor symptoms
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Yu, R.-L. and Wu, R.-M. and Tai, C.-H. and Lin, C.-H. and Hua, M.-S.; Yu, Rwei-Ling;Wu, Ruey-Meei;Tai, Chun-Hwei;Lin, Chin-Hsien;Hua, Mau-Sun; Yu, Rwei-Ling; Ruey-Meei Wu; CHUN-HWEI TAI; Wu, Ruey-Meei; Tai, Chun-Hwei; Chin-Hsien Lin; Lin, Chin-Hsien; Hua, Mau-Sun |
| 臺大學術典藏 |
2018-09-10T08:05:05Z |
A novel neuropsychiatric phenotype of KCNJ2 mutation in one Taiwanese family with Andersen-Tawil syndrome
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Jen-Jen Su; Chin-Hsien Lin; Chan, H.-F. and Chen, M.-L. and Su, J.-J. and Ko, L.-C. and Lin, C.-H. and Wu, R.-M.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T08:05:05Z |
An independent replication of park16 in asian samples
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Vilariño-Güell, C. and Ross, O.A. and Aasly, J.O. and White, L.R. and Rajput, A. and Rajput, A.H. and Lynch, T. and Krygowska-Wajs, A. and Jasinska-Myga, B. and Opala, G. and Barcikowska, M. and Lee, M.-C. and Hentati, F. and Uitti, R.J. and Wszolek, Z.K. and Farrer, M.J. and Wu, R.-M.; 李美靜;吳瑞美; Vilarino-Guell, C.; Ross, O. A.; Aasly, J. O.; White, L. R.; Rajput, A.; Rajput, A. H.; Lynch, T.; Krygowska-Wajs, A.; Jasinska-Myga, B.; Opala, G.; Barcikowska, M.; Lee, M.- C.; Hentati, F.; Uitti, R. J.; Wszolek, Z. K.; Ruey-Meei Wu; Vilarino-Guell, C.; Ross, O. A.; Aasly, J. O.; White, L. R.; Rajput, A.; Rajput, A. H.; Lynch, T.; Krygowska-Wajs, A.; Jasinska-Myga, B.; Opala, G.; Barcikowska, M.; Lee, M.- C.; Hentati, F.; Uitti, R. J.; Wszolek, Z. K. |
| 臺大學術典藏 |
2018-09-10T08:05:05Z |
Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese
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Tan, E.K. and Lu, C.S. and Peng, R. and Teo, Y.Y. and Wu-Chou, Y.H. and Chen, R.S. and Weng, Y.H. and Chen, C.M. and Fung, H.C. and Tan, L.C. and Zhang, Z.J. and An, X.K. and Lee-Chen, G.J. and Lee, M.C. and Fook-Chong, S. and Burgunder, J.M. and Wu, R.M. and Wu, Y.R.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T08:05:05Z |
Association of pyridoxal kinase and parkinson disease
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Vilariño-Güell, C. and Wider, C. and Aasly, J.O. and White, L.R. and Rajput, A. and Rajput, A.H. and Lynch, T. and Krygowska-Wajs, A. and Jasinska-Myga, B. and Opala, G. and Barcikowska, M. and Czyzewski, K. and Wu, R.-M. and Uitti, R.J. and Wszolek, Z.K. and Farrer, M.J. and Ross, O.A.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T08:05:05Z |
Deep brain stimulation therapy for Parkinson's disease using frameless stereotaxy: Comparison with frame-based surgery
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Tai, C.-H. and Wu, R.-M. and Lin, C.-H. and Pan, M.-K. and Chen, Y.-F. and Liu, H.-M. and Lu, H.-H. and Tsai, C.-W. and Tseng, S.-H.; Ruey-Meei Wu; CHUN-HWEI TAI; Ming-Kai Pan; YA-FANG CHEN; Chin-Hsien Lin; HON-MAN LIU |
| 臺大學術典藏 |
2018-09-10T07:32:11Z |
Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism
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Lee, M.-J. and Mata, I.F. and Lin, C.-H. and Tzen, K.-Y. and Lincoln, S.J. and Bounds, R. and Lockhart, P.J. and Hulihan, M.M. and Farrer, M.J. and Wu, R.-M.; 李銘仁;林靜嫻;曾凱元;吳瑞美; Lee, Ming-Jen; Mata, Ignacio F.; Lin, Chin-Hsien; Tzen, Kai-Yuan; Lincoln, Sarah J.; Bounds, Rebecca; Lockhart, Paul J.; Hulihan, Mary M.; Farrer, Matthew J.; Wu, Ruey-Meei; Ruey-Meei Wu; Chin-Hsien Lin; KAI-YUAN TZEN; MING-JEN LEE; Lee, Ming-Jen; Mata, Ignacio F.; Lin, Chin-Hsien; Tzen, Kai-Yuan; Lincoln, Sarah J.; Bounds, Rebecca; Lockhart, Paul J.; Hulihan, Mary M.; Farrer, Matthew J.; Wu, Ruey-Meei |
| 臺大學術典藏 |
2018-09-10T07:22:50Z |
Non-synonymous GIGYF2 variants in Parkinson's disease from two Asian populations
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Tan, E.-K. and Lin, C.-H. and Tai, C.-H. and Tan, L.C. and Chen, M.-L. and Li, R. and Lim, H.-Q. and Pavanni, R. and Yuen, Y. and Prakash, K.M. and Zhao, Y. and Wu, R.-M.; Ruey-Meei Wu; CHUN-HWEI TAI |
| 臺大學術典藏 |
2018-09-10T07:22:50Z |
CPP antagonizes hypoxia-induced changes in dopamine metabolism in the striatum of newborn rat
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Kuo, M.-F.;Wu, R.-M.;Wang, H.-S.;Lin, S.-M.; Ruey-Meei Wu; MENG-FAI KUO |
| 臺大學術典藏 |
2018-09-10T07:22:49Z |
Analysis of PArkin Co-Regulated Gene in a Taiwanese-Ethnic Chinese cohort with early-onset Parkinson's disease
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Taylor, J.M. and Wu, R.-M. and Farrer, M.J. and Delatycki, M.B. and Lockhart, P.J.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T07:22:49Z |
Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation
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Tai, Chun-Hwei;Yen, Ruoh-Fan;Lin, Chin-Hsien;Yen, Kuo-Yang;Yip, Ping-Keung;Wu, Ruey-Meei;Lee, Ming-Jen; Tai, C.-H. and Yen, R.-F. and Lin, C.-H. and Yen, K.-Y. and Yip, P.-K. and Wu, R.-M. and Lee, M.-J.; Tai, Chun-Hwei; Ruey-Meei Wu; CHUN-HWEI TAI; Yen, Ruoh-Fan; Lin, Chin-Hsien; RUOH-FANG YEN; Chin-Hsien Lin; Yen, Kuo-Yang; Yip, Ping-Keung; MING-JEN LEE; Wu, Ruey-Meei; Lee, Ming-Jen |
| 臺大學術典藏 |
2018-09-10T07:22:49Z |
GCH1 in early-onset Parkinson's disease
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Cobb, S.A. and Wider, C. and Ross, O.A. and Mata, I.F. and Adler, C.H. and Rajput, A. and Rajput, A.H. and Wu, R.-M. and Hauser, R. and Josephs, K.A. and Carr, J. and Gwinn, K. and Heckman, M.G. and Aasly, J.O. and Lynch, T. and Uitti, R.J. and Wszolek, Z.K. and Kapatos, G. and Farrer, M.J.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T07:22:49Z |
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism
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Ross, O.A. and Spanaki, C. and Griffith, A. and Lin, C.-H. and Kachergus, J. and Haugarvoll, K. and Latsoudis, H. and Plaitakis, A. and Ferreira, J.J. and Sampaio, C. and Bonifati, V. and Wu, R.-M. and Zabetian, C.P. and Farrer, M.J.; Ruey-Meei Wu; Chin-Hsien Lin |
| 臺大學術典藏 |
2018-09-10T07:22:49Z |
Lack of evidence for association of a parkin promoter polymorphism with early-onset Parkinson's disease in a Chinese population
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Taylor, J.M. and Wu, R.-M. and Lin, C.-H. and Delatycki, M.B. and Lockhart, P.J.; 吳瑞美;林靜嫻; Taylor, Juliet M.; Wu, Ruey-Meei; Lin, Chin-Hsien; Delatycki, Martin B.; Lockhart, Paul J.; Ruey-Meei Wu; Chin-Hsien Lin; Taylor, Juliet M.; Wu, Ruey-Meei; Lin, Chin-Hsien; Delatycki, Martin B.; Lockhart, Paul J. |
| 臺大學術典藏 |
2018-09-10T07:22:49Z |
LRRK2 G2385R modulates age at onset in Parkinson's disease: A multi-center pooled analysis
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Tan, E.K. and Peng, R. and Wu, Y.R. and Wu, R.M. and Wu-Chou, Y.H. and Tan, L.C. and An, X.K. and Chen, C.M. and Fook-Chong, S. and Lu, C.S.; 吳逸如;吳瑞美;陸清松; Tan, E.K.; Peng, R.; Wu, Y.R.; Wu, R.M.; Wu-Chou, Y.H.; Tan, L.C.; An, X.K.; Chen, C.M.; Fook-Chong, S.; Lu, C.S.; Ruey-Meei Wu; Tan, E.K.; Peng, R.; Wu, Y.R.; Wu, R.M.; Wu-Chou, Y.H.; Tan, L.C.; An, X.K.; Chen, C.M.; Fook-Chong, S.; Lu, C.S. |
| 臺大學術典藏 |
2018-09-10T06:50:44Z |
LRRK2 mutation in familial Parkinson's disease in a Taiwanese population: Clinical, PET, and functional studies
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Lin, C.-H. and Tzen, K.-Y. and Yu, C.-Y. and Tai, C.-H. and Farrer, M.J. and Wu, R.-M.; Ruey-Meei Wu; CHUN-HWEI TAI; KAI-YUAN TZEN; Chin-Hsien Lin |
| 臺大學術典藏 |
2018-09-10T06:50:44Z |
Lrrk2 R1628P in non-Chinese Asian races
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Tan, E.-K. and Tang, M. and Tan, L.C. and Wu, Y.-R. and Wu, R.-M. and Ross, O.A. and Zhao, Y.; 吳逸如;吳瑞美; Tan, Eng-King; Tang, Michelle; Tan, Louis C.; Wu, Yih-Ru; Wu, Ruey-Meei; Ross, Owen A.; Zhao, Yi; Ruey-Meei Wu; Tan, Eng-King; Tang, Michelle; Tan, Louis C.; Wu, Yih-Ru; Wu, Ruey-Meei; Ross, Owen A.; Zhao, Yi |
| 臺大學術典藏 |
2018-09-10T06:50:44Z |
Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore
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Lin, C.H. and Tan, E.K. and Chen, M.L. and Tan, L.C. and Lim, H.Q. and Chen, G.S. and Wu, R.M.; Ruey-Meei Wu; Chin-Hsien Lin |
| 臺大學術典藏 |
2018-09-10T06:50:43Z |
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease
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Ross, O.A. and Wu, Y.-R. and Lee, M.-C. and Funayama, M. and Chen, M.-L. and Soto, A.I. and Mata, I.F. and Lee-Chen, G.-J. and Chiung, M.C. and Tang, M. and Zhao, Y. and Hattori, N. and Farrer, M.J. and Tan, E.-K. and Wu, R.-M.; 吳逸如;李美靜;陳孟伶;李桂楨;陳瓊美;吳瑞美; Ross, Owen A.; Wu, Yih-Ru; Lee, Mei-Ching; Funayama, Manabu; Chen, Meng-Ling; Soto, Alexandra I.; Mata, Ignacio F.; Lee-Chen, Guey-Jen; Chen, Chiung Mei; Tang, Michelle; Zhao, Yi; Hattori, Nobutaka; Farrer, Matthew J.; Tan, Eng-King; Wu, Ruey-Meei; Ruey-Meei Wu; Ross, Owen A.; Wu, Yih-Ru; Lee, Mei-Ching; Funayama, Manabu; Chen, Meng-Ling; Soto, Alexandra I.; Mata, Ignacio F.; Lee-Chen, Guey-Jen; Chen, Chiung Mei; Tang, Michelle; Zhao, Yi; Hattori, Nobutaka; Farrer, Matthew J.; Tan, Eng-King; Wu, Ruey-Meei |
| 臺大學術典藏 |
2018-09-10T06:50:32Z |
Neurocysticercosis presenting with epilepsia partialis continua: A clinicopathologic report and literature review
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葉馨喬;吳瑞美; Yeh, S.-J. and Wu, R.-M.; YEH, SHIN-JOE;WU, RUEY-MEEI; Ruey-Meei Wu; Shin-Joe Yeh; YEH, SHIN-JOE; WU, RUEY-MEEI |
| 臺大學術典藏 |
2018-09-10T06:40:07Z |
Acute disseminated encephalomyelitis: A follow-up study in Taiwan
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Lin, CH;Jeng, JS;Hsieh, ST;Yip, PK;Wu, RM.; Lin, C.-H. and Jeng, J.-S. and Hsieh, S.-T. and Yip, P.-K. and Wu, R.-M.; Ruey-Meei Wu; Lin, CH; Jeng, JS; JIANN-SHING JENG; SUNG-TSANG HSIEH; Hsieh, ST; Yip, PK; Chin-Hsien Lin; Wu, RM. |
| 臺大學術典藏 |
2018-09-10T06:15:22Z |
Transcranial imaging of substantia nigra hyperechogenicity in a Taiwanese cohort of Parkinson's disease
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Huang, Y.-W. and Jeng, J.-S. and Tsai, C.-F. and Chen, L.-L. and Wu, R.-M.; Ruey-Meei Wu; JIANN-SHING JENG |
| 臺大學術典藏 |
2018-09-10T06:15:21Z |
Common variants in Parkinson's disease [2]
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Ross, O.A. and Farrer, M.J. and Wu, R.-M.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T06:15:21Z |
Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (Ethnic Chinese) cohort of familial and early-onset parkinsonism
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Lin, C.-H. and Hwu, W.-L. and Chiang, S.-C. and Tai, C.-H. and Wu, R.-M.; Ruey-Meei Wu; CHUN-HWEI TAI; Chin-Hsien Lin; WUH-LIANG HWU |
| 臺大學術典藏 |
2018-09-10T06:15:21Z |
Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia
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Farrer, M.J. and Stone, J.T. and Lin, C.-H. and Dächsel, J.C. and Hulihan, M.M. and Haugarvoll, K. and Ross, O.A. and Wu, R.-M.; Ruey-Meei Wu; Chin-Hsien Lin |
| 臺大學術典藏 |
2018-09-10T06:15:21Z |
Pesticide exposure on southwestern Taiwanese with MnSOD and NQO1 polymorphisms is associated with increased risk of Parkinson's disease
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Fong, C.-S. and Wu, R.-M. and Shieh, J.-C. and Chao, Y.-T. and Fu, Y.-P. and Kuao, C.-L. and Cheng, C.-W.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T06:15:21Z |
The SCA17 phenotype can include features of MSA-C, PSP and cognitive impairment
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Ruey-Meei Wu; Lin, I.-S. and Wu, R.-M. and Lee-Chen, G.-J. and Shan, D.-E. and Gwinn-Hardy, K. |
| 臺大學術典藏 |
2018-09-10T06:15:21Z |
Transcranial color-coded sonography helps differentiation between idiopathic Parkinson's disease and vascular parkinsonism
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Tsai, C.-F. and Wu, R.-M. and Huang, Y.-W. and Chen, L.-L. and Yip, P.-K. and Jeng, J.-S.; Ruey-Meei Wu; JIANN-SHING JENG |
| 臺大學術典藏 |
2018-09-10T05:47:09Z |
Suppression of hydroxyl radical formation and protection of nigral neurons by l-deprenyl (selegiline)
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Wu, R.-M. and Murphy, D.L. and Chiueh, C.C.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T05:47:08Z |
Bilateral deep brain stimulation of subthalamic nucleus alleviates tardive dystonia
|
Tai, C.-H. and Tseng, S.-H. and Liu, H.-M. and Wu, R.-M.; Ruey-Meei Wu; CHUN-HWEI TAI; HON-MAN LIU |
| 臺大學術典藏 |
2018-09-10T05:12:51Z |
Lrrk2 pathogenic substitutions in Parkinson's disease
|
Mata, I.F. and Kachergus, J.M. and Taylor, J.P. and Lincoln, S. and Aasly, J. and Lynch, T. and Hulihan, M.M. and Cobb, S.A. and Wu, R.-M. and Lu, C.-S. and Lahoz, C. and Wszolek, Z.K. and Farrer, M.J.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T05:12:51Z |
Parkin mutations and early-onset parkinsonism in a Taiwanese cohort
|
Wu, R.-M. and Bounds, R. and Lincoln, S. and Hulihan, M. and Lin, C.-H. and Hwu, W.-L. and Chen, J. and Gwinn-Hardy, K. and Farrer, M.; Ruey-Meei Wu; Chin-Hsien Lin; WUH-LIANG HWU |
| 臺大學術典藏 |
2018-09-10T05:12:51Z |
Pesticides exposure and genetic polymorphism of paraoxonase in the susceptibility of Parkinson's disease
|
Fong, C.-S. and Cheng, C.-W. and Wu, R.-M.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T05:12:51Z |
Neuronal protective and rescue effects of deprenyl against MPP+ dopaminergic toxicity
|
Wu, R.-M. and Murphy, D.L. and Chiueh, C.C.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T04:44:27Z |
Selegiline (l-deprenyl) as a unique neuroprotective agent for chronic neurodegenerative disorders - A lesson from MAO inhibition
|
Wu, Ruey-Meei;Murphy, Dennis L;Chiueh, Chuang C; Wu, R.-M. and Murphy, D.L. and Chiueh, C.C.; Wu, Ruey-Meei; Ruey-Meei Wu; Murphy, Dennis L; Chiueh, Chuang C |
| 臺大學術典藏 |
2018-09-10T04:44:27Z |
[125I]CGP 42112 reveals a non-angiotensin II binding site in 1-methyl-4-phenylpyridine (MPP+)-induced brain injury
|
Viswanathan, M. and de Oliverira, A.M. and Wu, R.-M. and Chiueh, C.C. and Saavedra, J.M.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T04:44:27Z |
Ferrous-citrate complier and nigral degeneration: Evidence for free-radical formation and lipid peroxidation
|
Mohanakumar, K.P. and De Bartolomeis, A. and Wu, R.-M. and Yeh, K.J. and Sternberger, L.M. and Peng, S.-Y. and Murphy, D.L. and Chiueh, C.C.; Ruey-Meei Wu |
| 臺大學術典藏 |
2018-09-10T04:44:27Z |
In vivo generation of hydroxyl radicals and MPTP-induced dopaminergic toxicity in the basal ganglia
|
Chiueh, C.C. and Wu, R.-M. and Mohanakumar, K.P. and Sternberger, L.M. and Krishna, G. and Obata, T. and Murphy, D.L.; Ruey-Meei Wu |
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