臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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Institution	Date	Title	Author
臺大學術典藏	2020-03-04T07:45:30Z	Generation of 2 induced pluripotent stem cell lines derived from patients with Parkinson's disease carrying LRRK2 G2385R variant	Hsu Y.-H.; Syu S.-H.; Lu H.-E.; Lin H.-I.; CHIN-HSIEN LIN; Hsieh P.C.H.; Huang C.-Y.; Ho M.-C.; Cheng Y.-C.
臺大學術典藏	2020-03-04T07:45:25Z	Craniocervical dystonia with levodopa-responsive parkinsonism co-segregating with a pathogenic ANO3 mutation in a Taiwanese family	Kuo M.-C.; Lin H.-I.; CHIN-HSIEN LIN
臺大學術典藏	2020-03-04T07:45:25Z	Catechol-O-methyltransferase (COMT) genetic variants are associated with cognitive decline in patients with Parkinson's disease	CHIN-HSIEN LIN; Fan J.-Y.; Lin H.-I.; Chang C.-W.; Wu Y.-R.
臺大學術典藏	2020-03-04T07:45:25Z	Clinical heterogeneity of LRRK2 p.I2012T mutation	Fan T.-S.; Wu R.-M.; Chen P.-L.; Chen T.-F.; Li H.-Y.; Lin Y.-H.; Chen C.-Y.; Chen M.-L.; Tai C.-H.; Lin H.-I.; CHIN-HSIEN LIN
臺大學術典藏	2020-03-04T07:45:24Z	The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease.	Wu R.M.; CHIN-HSIEN LIN; Lin H.I.
臺大學術典藏	2020-03-04T07:45:23Z	Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population	Fan T.-S.; Lin H.-I.; CHIN-HSIEN LIN; Wu R.-M.
臺大學術典藏	2020-03-04T07:45:23Z	COQ2 p.V393A variant, rs148156462, is not associated with Parkinson's disease in a Taiwanese population	CHIN-HSIEN LIN; Lin H.-I.; Chen M.-L.; Wu R.-M.
臺大學術典藏	2020-03-04T07:45:23Z	Vitamin D receptor genetic variants and Parkinson's disease in a Taiwanese population	CHIN-HSIEN LIN; Chen K.-H.; Chen M.-L.; Lin H.-I.; Wu R.-M.
臺大學術典藏	2020-03-04T07:45:22Z	PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population	Fan T.-S.; Wu R.-M.; Lin H.-I.; Cheng C.; CHIN-HSIEN LIN
臺大學術典藏	2020-03-04T07:45:22Z	Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort	Lin H.-H.; Wu R.-M.; Lin H.-I.; Chen M.-L.; Tai C.-H.; CHIN-HSIEN LIN

Showing items 86-95 of 155 (16 Page(s) Totally)
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