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机构 日期 题名 作者
臺大學術典藏 2020-03-04T07:45:20Z Population-specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO-PD) consortium 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.; CHIN-HSIEN LIN; Lynch T.; Maraganore D.M.; Mellick G.D.; Mutez E.; Nilsson C.; 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.; Wu R.-M.; Hentati F.; Farrer M.J.; Ross O.A.
臺大學術典藏 2020-03-04T07:45:15Z Lovastatin protects neurite degeneration in LRRK2-G2019S parkinsonism through activating the Akt/Nrf pathway and inhibiting GSK3�] activity CHIN-HSIEN LIN; Lin H.-I.; Chen M.-L.; Lai T.-T.; Cao L.-P.; Farrer M.J.; Wu R.-M.; Chien C.-T.
臺大學術典藏 2020-03-04T07:45:15Z LRRK2 mutation in familial Parkinson's disease in a Taiwanese population: Clinical, PET, and functional studies CHIN-HSIEN LIN; Tzen K.-Y.; Yu C.-Y.; Tai C.-H.; Farrer M.J.; Wu R.-M.
臺大學術典藏 2020-03-03T02:33:33Z Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism MING-JEN LEE; Mata I.F.; Lin C.-H.; Tzen K.-Y.; Lincoln S.J.; Bounds R.; Lockhart P.J.; Hulihan M.M.; Farrer M.J.; Wu R.-M.
臺大學術典藏 2020-02-25T08:01:45Z Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism Lockhart P.J;Bounds R;Hulihan M;Kachergus J;Lincoln S;Lin C.-H;Ruey-Meei Wu;Farrer M.J.; Lockhart P.J; Bounds R; Hulihan M; Kachergus J; Lincoln S; Lin C.-H; RUEY-MEEI WU; Farrer M.J.
臺大學術典藏 2020-02-25T08:01:45Z Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism Lockhart P.J;Bounds R;Hulihan M;Kachergus J;Lincoln S;Lin C.-H;Ruey-Meei Wu;Farrer M.J.; Lockhart P.J; Bounds R; Hulihan M; Kachergus J; Lincoln S; Lin C.-H; RUEY-MEEI WU; Farrer M.J.
臺大學術典藏 2020-02-25T08:01:44Z Lrrk2 pathogenic substitutions in Parkinson's disease Cobb S.A; RUEY-MEEI WU; Lu C.-S; Lahoz C; Wszolek Z.K; Farrer M.J.; Hulihan M.M; Mata I.F;Kachergus J.M;Taylor J.P;Lincoln S;Aasly J;Lynch T;Hulihan M.M;Cobb S.A;Ruey-Meei Wu;Lu C.-S;Lahoz C;Wszolek Z.K;Farrer M.J.; Mata I.F; Kachergus J.M; Taylor J.P; Lincoln S; Aasly J; Lynch T
臺大學術典藏 2020-02-25T08:01:44Z Lrrk2 pathogenic substitutions in Parkinson's disease Cobb S.A; RUEY-MEEI WU; Lu C.-S; Lahoz C; Wszolek Z.K; Farrer M.J.; Hulihan M.M; Mata I.F;Kachergus J.M;Taylor J.P;Lincoln S;Aasly J;Lynch T;Hulihan M.M;Cobb S.A;Ruey-Meei Wu;Lu C.-S;Lahoz C;Wszolek Z.K;Farrer M.J.; Mata I.F; Kachergus J.M; Taylor J.P; Lincoln S; Aasly J; Lynch T
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 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

显示项目 21-30 / 59 (共6页)
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