English  |  正體中文  |  简体中文  |  總筆數 :0  
造訪人次 :  51632486    線上人數 :  951
教育部委託研究計畫      計畫執行:國立臺灣大學圖書館
 
臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
關於TAIR

瀏覽

消息

著作權

相關連結

"farrer m j"的相關文件

回到依作者瀏覽
依題名排序 依日期排序

顯示項目 41-50 / 59 (共6頁)
<< < 1 2 3 4 5 6 > >>
每頁顯示[10|25|50]項目

機構 日期 題名 作者
臺大學術典藏 2020-02-25T08:01:32Z Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: A case-control study Ross O.A; Soto-Ortolaza A.I; Heckman M.G; Aasly J.O; Abahuni N; Annesi G; Bacon J.A; Bardien S; Bozi M; Brice A; Brighina L; Van Broeckhoven C; Carr J; Chartier-Harlin M.-C; Dardiotis E; Dickson D.W; Diehl N.N; Elbaz A; Ferrarese C; Ferraris A; Fiske B; Gibson J.M; Gibson R; Hadjigeorgiou G.M; Hattori N; Ioannidis J.P.A; Jasinska-Myga B; Jeon B.S; Kim Y.J; Klein C; Kruger R; Kyratzi E; Lesage S; Lin C.-H; Lynch T; Maraganore D.M; Mellick G.D; Mutez E; Nilsson C; Opala G; Park S.S; Puschmann A; Quattrone A; Sharma M; Silburn P.A; Sohn Y.H; Stefanis L; Tadic V; Theuns J; Tomiyama H; Uitti R.J; Valente E.M; van de Loo S; Vassilatis D.K; Vilari?o-G?ell C; White L.R; Wirdefeldt K; Wszolek Z.K; RUEY-MEEI WU; Farrer M.J.
臺大學術典藏 2020-02-25T08:01:31Z VPS35 mutations in parkinson disease Vilari?O-G?Ell C;Wider C;Ross O.A;Dachsel J.C;Kachergus J.M;Lincoln S.J;Soto-Ortolaza A.I;Cobb S.A;Wilhoite G.J;Bacon J.A;Bahareh Behrouz, Melrose H.L;Hentati E;Puschmann A;Evans D.M;Conibear E;Wasserman W.W;Aasly J.O;Burkhard P.R;Djaldetti R;Ghika J;Hentati F;Krygowska-Wajs A;Lynch T;Melamed E;Rajput A;Rajput A.H;Solida A;Ruey-Meei Wu;Uitti R.J;Wszolek Z.K;Vingerhoets F;Farrer M.J.; Vilari?o-G?ell C; Wider C; Ross O.A; Dachsel J.C; Kachergus J.M; Lincoln S.J; Soto-Ortolaza A.I; Cobb S.A; Wilhoite G.J; Bacon J.A; Bahareh Behrouz, Melrose H.L; Hentati E; Puschmann A; Evans D.M; Conibear E; Wasserman W.W; Aasly J.O; Burkhard P.R; Djaldetti R; Ghika J; Hentati F; Krygowska-Wajs A; Lynch T; Melamed E; Rajput A; Rajput A.H; Solida A; RUEY-MEEI WU; Uitti R.J; Wszolek Z.K; Vingerhoets F; Farrer M.J.
臺大學術典藏 2020-02-25T08:01:31Z VPS35 mutations in parkinson disease Vilari?O-G?Ell C;Wider C;Ross O.A;Dachsel J.C;Kachergus J.M;Lincoln S.J;Soto-Ortolaza A.I;Cobb S.A;Wilhoite G.J;Bacon J.A;Bahareh Behrouz, Melrose H.L;Hentati E;Puschmann A;Evans D.M;Conibear E;Wasserman W.W;Aasly J.O;Burkhard P.R;Djaldetti R;Ghika J;Hentati F;Krygowska-Wajs A;Lynch T;Melamed E;Rajput A;Rajput A.H;Solida A;Ruey-Meei Wu;Uitti R.J;Wszolek Z.K;Vingerhoets F;Farrer M.J.; Vilari?o-G?ell C; Wider C; Ross O.A; Dachsel J.C; Kachergus J.M; Lincoln S.J; Soto-Ortolaza A.I; Cobb S.A; Wilhoite G.J; Bacon J.A; Bahareh Behrouz, Melrose H.L; Hentati E; Puschmann A; Evans D.M; Conibear E; Wasserman W.W; Aasly J.O; Burkhard P.R; Djaldetti R; Ghika J; Hentati F; Krygowska-Wajs A; Lynch T; Melamed E; Rajput A; Rajput A.H; Solida A; RUEY-MEEI WU; Uitti R.J; Wszolek Z.K; Vingerhoets F; Farrer M.J.
臺大學術典藏 2020-02-25T08:01:30Z Erratum: VPS35 mutations in Parkinson disease (American Journal of Human Genetics (2011) 89 (162-167)) Vilari?o-G?ell C; Wider C; Ross O.A; Dachsel J.C; Kachergus J.M; Lincoln S.J; Soto-Ortolaza A.I; Cobb S.A; Wilhoite G.J; Bacon J.A; Behrouz B; Melrose H.L; Hentati E; Puschmann A; Evans D.M; Conibear E; Wasserman W.W; Aasly J.O; Burkhard P.R; Djaldetti R; Ghika J; Hentati F; Krygowska-Wajs A; Lynch T; Melamed E; Rajput A; Rajput A.H; Solida A; RUEY-MEEI WU; Uitti R.J; Wszolek Z.K; Vingerhoets F; Farrer M.J.
臺大學術典藏 2020-02-25T08:01:27Z STX6 rs1411478 is not associated with increased risk of Parkinson's disease Trinh J; Vilari?o-G?ell C; Donald A; Shah B; Yu I; Szu-Tu C; Aasly J.O; RUEY-MEEI WU; Hentati F; Rajput A.H; Rajput A; Farrer M.J.
臺大學術典藏 2020-02-25T08:01:26Z Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium Opala G; Park S.S; Petrucci S; Puschmann A; Quattrone A; Sharma M; Silburn P.A; Sohn Y.H; Stefanis L; Tadic V; Theuns J; Tomiyama H; Uitti R.J; Valente E.M; Van Broeckhoven C; Van De Loo S; Vassilatis D.K; Vilari?o-G?ell C; White L.R; Wirdefeldt K; Wszolek Z.K; RUEY-MEEI WU; Hentati F; Farrer M.J; Ross O.A.; Nilsson C; Mutez E; Mellick G.D; Heckman M.G; Soto-Ortolaza A.I; Aasly J.O; Abahuni N; Annesi G; Bacon J.A; Bardien S; Bozi M; Brice A; Brighina L; Carr J; Chartier-Harlin M.-C; Dardiotis E; Dickson D.W; Diehl N.N; Elbaz A; Ferrarese C; Fiske B; Gibson J.M; Gibson R; Hadjigeorgiou G.M; Hattori N; Ioannidis J.P.A; Boczarska-Jedynak M; Jasinska-Myga B; Jeon B.S; Kim Y.J; Klein C; Kruger R; Kyratzi E; Lesage S; Lin C.-H; Lynch T; Maraganore D.M
臺大學術典藏 2020-02-25T08:01:25Z The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants Heckman M.G; Elbaz A; Soto-Ortolaza A.I; Serie D.J; Aasly J.O; Annesi G; Auburger G; Bacon J.A; Boczarska-Jedynak M; Bozi M; Brighina L; Chartier-Harlin M.-C; Dardiotis E; Dest?e A; Ferrarese C; Ferraris A; Fiske B; Gispert S; Hadjigeorgiou G.M; Hattori N; Ioannidis J.P.A; Jasinska-Myga B; Jeon B.S; Kim Y.J; Klein C; Kruger R; Kyratzi E; Lin C.-H; Lohmann K; Loriot M.-A; Lynch T; Mellick G.D; Mutez E; Opala G; Park S.S; Petrucci S; Quattrone A; Sharma M; Silburn P.A; Sohn Y.H; Stefanis L; Tadic V; Tomiyama H; Uitti R.J; Valente E.M; Vassilatis D.K; Vilari?o-G?ell C; White L.R; Wirdefeldt K; Wszolek Z.K; RUEY-MEEI WU; Xiromerisiou G; Maraganore D.M; Farrer M.J; Ross O.A.
臺大學術典藏 2020-02-25T08:01:24Z DNAJC13 mutations in Parkinson disease Vilari?o-G?ell C; Rajput A; Milnerwood A.J; Shah B; Szu-Tu C; Trinh J; Yu I; Encarnacion M; Munsie L.N; Tapia L; Gustavsson E.K; Chou P; Tatarnikov I; Evans D.M; Pishotta F.T; Volta M; Beccano-Kelly D; Thompson C; Lin M.K; Sherman H.E; Han H.J; Guenther B.L; Wasserman W.W; Bernard V; Ross C.J; Appel-Cresswell S; Stoessl A.J; Robinson C.A; Dickson D.W; Ross O.A; Wszolek Z.K; Aasly J.O; RUEY-MEEI WU; Hentati F; Gibson R.A; McPherson P.S; Girard M; Rajput M; Rajput A.H; Farrer M.J.
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 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.

顯示項目 41-50 / 59 (共6頁)
<< < 1 2 3 4 5 6 > >>
每頁顯示[10|25|50]項目