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Showing items 91-115 of 155 (7 Page(s) Totally)
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Institution	Date	Title	Author
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
臺大學術典藏	2020-03-04T07:45:22Z	Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese population	Chen K.-H.; Wu R.-M.; Lin H.-I.; Tai C.-H.; CHIN-HSIEN LIN
臺大學術典藏	2020-03-04T07:45:20Z	A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing	CHIN-HSIEN LIN; Chen P.-L.; Tai C.-H.; Lin H.-I.; Chen C.-S.; Chen M.-L.; Wu R.-M.
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	2020-03-04T07:45:14Z	Lack of C9orf72 repeat expansion in Taiwanese patients with mixed neurodegenerative disorders	CHIN-HSIEN LIN; Chen T.-F.; Chiu M.-J.; Lin H.-I.; Wu R.-M.
臺大學術典藏	2020-03-04T07:45:12Z	A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: A case study and literature review	Hsueh S.-J.; Lee N.-C.; Yang S.-H.; Lin H.-I.; CHIN-HSIEN LIN
臺大學術典藏	2020-03-04T07:45:10Z	Lack of TMEM230 mutations in patients with familial and sporadic Parkinson's disease in a Taiwanese population	Fan T.-S.; CHIN-HSIEN LIN; Lin H.-I.; Chen M.-L.; Wu R.-M.
臺大學術典藏	2020-03-04T05:35:00Z	Lack of C9orf72 repeat expansion in Taiwanese patients with mixed neurodegenerative disorders	Lin C.-H.; Chen T.-F.; MING-JANG CHIU; Lin H.-I.; Wu R.-M.
臺大學術典藏	2020-03-03T01:14:45Z	Lack of C9orf72 repeat expansion in Taiwanese patients with mixed neurodegenerative disorders	Lin C.-H; TA-FU CHEN; Chiu M.-J; Lin H.-I; Wu R.-M.
臺大學術典藏	2020-03-03T01:14:42Z	Clinical heterogeneity of LRRK2 p.I2012T mutation	Fan T.-S; Wu R.-M; Chen P.-L; TA-FU CHEN; Li H.-Y; Lin Y.-H; Chen C.-Y; Chen M.-L; Tai C.-H; Lin H.-I; Lin C.-H.
臺大學術典藏	2020-02-25T08:01:25Z	The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease.	RUEY-MEEI WU; Lin C.H; Lin H.I.
臺大學術典藏	2020-02-25T08:01:25Z	Vitamin D receptor genetic variants and Parkinson's disease in a Taiwanese population	Lin C.-H; Chen K.-H; Chen M.-L; Lin H.-I; RUEY-MEEI WU
臺大學術典藏	2020-02-25T08:01:25Z	Lack of C9orf72 repeat expansion in Taiwanese patients with mixed neurodegenerative disorders	Lin C.-H; Chen T.-F; Chiu M.-J; Lin H.-I; RUEY-MEEI WU
臺大學術典藏	2020-02-25T08:01:23Z	COQ2 p.V393A variant, rs148156462, is not associated with Parkinson's disease in a Taiwanese population	Lin C.-H; Lin H.-I; Chen M.-L; RUEY-MEEI WU
臺大學術典藏	2020-02-25T08:01:22Z	Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese population	Chen K.-H;Ruey-Meei Wu;Lin H.-I;Tai C.-H;Lin C.-H.; Chen K.-H; RUEY-MEEI WU; Lin H.-I; Tai C.-H; Lin C.-H.
臺大學術典藏	2020-02-25T08:01:22Z	Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population	Fan T.-S;Lin H.-I;Lin C.-H;Ruey-Meei Wu; Fan T.-S; Lin H.-I; Lin C.-H; RUEY-MEEI WU
臺大學術典藏	2020-02-25T08:01:20Z	Lovastatin protects neurite degeneration in LRRK2-G2019S parkinsonism through activating the Akt/Nrf pathway and inhibiting GSK3?] activity	Lin C.-H;Lin H.-I;Chen M.-L;Lai T.-T;Cao L.-P;Farrer M.J;Ruey-Meei Wu;Chien C.-T.; Lin C.-H; Lin H.-I; Chen M.-L; Lai T.-T; Cao L.-P; Farrer M.J; RUEY-MEEI WU; Chien C.-T.
臺大學術典藏	2020-02-25T08:01:19Z	Clinical heterogeneity of LRRK2 p.I2012T mutation	Fan T.-S;Ruey-Meei Wu;Chen P.-L;Chen T.-F;Li H.-Y;Lin Y.-H;Chen C.-Y;Chen M.-L;Tai C.-H;Lin H.-I;Lin C.-H.; Fan T.-S; RUEY-MEEI WU; Chen P.-L; Chen T.-F; Li H.-Y; Lin Y.-H; Chen C.-Y; Chen M.-L; Tai C.-H; Lin H.-I; Lin C.-H.
臺大學術典藏	2020-02-25T08:01:18Z	Lack of TMEM230 mutations in patients with familial and sporadic Parkinson's disease in a Taiwanese population	Fan T.-S;Lin C.-H;Lin H.-I;Chen M.-L;Ruey-Meei Wu; Fan T.-S; Lin C.-H; Lin H.-I; Chen M.-L; RUEY-MEEI WU
臺大學術典藏	2020-02-25T08:01:18Z	Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort	Lin H.-H;Ruey-Meei Wu;Lin H.-I;Chen M.-L;Tai C.-H;Lin C.-H.; Lin H.-H; RUEY-MEEI WU; Lin H.-I; Chen M.-L; Tai C.-H; Lin C.-H.
臺大學術典藏	2020-02-25T08:01:16Z	A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing	Lin C.-H;Chen P.-L;Tai C.-H;Lin H.-I;Chen C.-S;Chen M.-L;Ruey-Meei Wu; Lin C.-H; Chen P.-L; Tai C.-H; Lin H.-I; Chen C.-S; Chen M.-L; RUEY-MEEI WU

Showing items 91-115 of 155 (7 Page(s) Totally)
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