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Showing items 1531-1540 of 3227 (323 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2020-02-25T08:01:44Z	Parkin mutations and early-onset parkinsonism in a Taiwanese cohort	Ruey-Meei Wu;Bounds R;Lincoln S;Hulihan M;Lin C.-H;Hwu W.-L;Chen J;Gwinn-Hardy K;Farrer M.; RUEY-MEEI WU; Bounds R; Lincoln S; Hulihan M; Lin C.-H; Hwu W.-L; Chen J; Gwinn-Hardy K; Farrer M.
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	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	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
臺大學術典藏	2020-02-25T08:01:42Z	Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (Ethnic Chinese) cohort of familial and early-onset parkinsonism	Lin C.-H; Hwu W.-L; Chiang S.-C; Tai C.-H; RUEY-MEEI WU
臺大學術典藏	2020-02-25T08:01:40Z	Non-synonymous GIGYF2 variants in Parkinson's disease from two Asian populations	Tan E.-K; Lin C.-H; Tai C.-H; Tan L.C; Chen M.-L; Li R; Lim H.-Q; Pavanni R; Yuen Y; Prakash K.M; Zhao Y; RUEY-MEEI WU
臺大學術典藏	2020-02-25T08:01:40Z	Lack of evidence for association of a parkin promoter polymorphism with early-onset Parkinson's disease in a Chinese population	Lockhart P.J.;Delatycki M.B;Lin C.-H;RUEY-MEEI WU;Taylor J.M; Taylor J.M; RUEY-MEEI WU; Lin C.-H; Delatycki M.B; Lockhart P.J.
臺大學術典藏	2020-02-25T08:01:40Z	Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism	Lee M.-J; Mata I.F; Lin C.-H; Tzen K.-Y; Lincoln S.J; Bounds R; Lockhart P.J; Hulihan M.M; Farrer M.J; RUEY-MEEI WU
臺大學術典藏	2020-02-25T08:01:37Z	Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation	Tai C.-H; Yen R.-F; Lin C.-H; Yen K.-Y; Yip P.-K; RUEY-MEEI WU; Lee M.-J.

Showing items 1531-1540 of 3227 (323 Page(s) Totally)
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