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

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Showing items 56-65 of 155 (16 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2020-11-03T12:12:43Z	Clinical heterogeneity of LRRK2 p.I2012T mutation	CHIN-HSIEN LIN; Lin H.-I.; Tai C.-H.; Chen C.-Y.; Chen M.-L.; Li H.-Y.; Lin Y.-H.; Chen T.-F.; Chen P.-L.; Wu R.-M.; Fan T.-S.
臺大學術典藏	2020-11-03T12:12:42Z	Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort	CHIN-HSIEN LIN; Tai C.-H.; Chen M.-L.; Lin H.-I.; Wu R.-M.; Lin H.-H.; Lin H.-H.;Wu R.-M.;Lin H.-I.;Chen M.-L.;Tai C.-H.;Chin-Hsien Lin
臺大學術典藏	2020-11-03T12:12:41Z	Lack of TMEM230 mutations in patients with familial and sporadic Parkinson's disease in a Taiwanese population	CHIN-HSIEN LIN; Lin H.-I.; Chen M.-L.; Wu R.-M.; Fan T.-S.; Fan T.-S.;Chin-Hsien Lin;Lin H.-I.;Chen M.-L.;Wu R.-M.
臺大學術典藏	2020-11-03T12:12:40Z	Generation of 2 induced pluripotent stem cell lines derived from patients with Parkinson's disease carrying LRRK2 G2385R variant	Hsieh P.C.H.; CHIN-HSIEN LIN; Lin H.-I.; Lu H.-E.; Syu S.-H.; Hsu Y.-H.; Ho M.-C.; Huang C.-Y.; Cheng Y.-C.; Cheng Y.-C.;Huang C.-Y.;Ho M.-C.;Hsu Y.-H.;Syu S.-H.;Lu H.-E.;Lin H.-I.;Chin-Hsien Lin;Hsieh P.C.H.
臺大學術典藏	2020-11-03T12:12:40Z	Depression and Catechol-O-methyltransferase (COMT) genetic variants are associated with pain in Parkinson's disease	Rizos A.; Chang C.-W.; Lin H.-I.; Wu Y.-R.; Ko C.-I.; Fan J.-Y.; Chaudhuri K.R.; CHIN-HSIEN LIN; Chin-Hsien Lin;Chaudhuri K.R.;Fan J.-Y.;Ko C.-I.;Rizos A.;Chang C.-W.;Lin H.-I.;Wu Y.-R.
臺大學術典藏	2020-11-03T12:12:39Z	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.; CHIN-HSIEN LIN; Fan J.-Y.; Lin H.-I.; Chang C.-W.; Wu Y.-R.
臺大學術典藏	2020-11-03T12:12:39Z	PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population	CHIN-HSIEN LIN; Fan T.-S.;Wu R.-M.;Lin H.-I.;Cheng C.;Chin-Hsien Lin; Fan T.-S.; Wu R.-M.; Lin H.-I.; Cheng C.
臺大學術典藏	2020-11-03T12:12:38Z	Generation of induced pluripotent stem cells (IBMSi011-A) from a patient with Parkinson's disease carrying LRRK2 p.I1371V mutation	Lin H.-I.;Cheng Y.-C.;Ko H.-W.;Wen C.-H.;Lu H.-E.;Huang C.-Y.;Hsieh P.C.H.;Chin-Hsien Lin; Lin H.-I.; Cheng Y.-C.; Ko H.-W.; Wen C.-H.; Lu H.-E.; Huang C.-Y.; Hsieh P.C.H.; CHIN-HSIEN LIN
臺大學術典藏	2020-11-03T12:12:38Z	Reprogramming of a human induced pluripotent stem cell (iPSC) line (IBMSi012-A) from an early-onset Parkinson's disease patient harboring a homozygous p.D331Y mutation in the PLA2G6 gene	Cheng Y.-C.;Lin H.-I.;Syu S.-H.;Lu H.-E.;Huang C.-Y.;Chin-Hsien Lin;Hsieh P.C.H.; Cheng Y.-C.; Lin H.-I.; Syu S.-H.; Hsieh P.C.H.; Lu H.-E.; Huang C.-Y.; CHIN-HSIEN LIN
臺大學術典藏	2020-11-03T12:12:38Z	A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing	Wu R.-M.; Chen M.-L.; Chin-Hsien Lin;Chen P.-L.;Tai C.-H.;Lin H.-I.;Chen C.-S.;Chen M.-L.;Wu R.-M.; CHIN-HSIEN LIN; Chen P.-L.; Tai C.-H.; Lin H.-I.; Chen C.-S.

Showing items 56-65 of 155 (16 Page(s) Totally)
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