| 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. |
| 臺大學術典藏 |
2020-11-03T12:12:37Z |
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; Kuo M.-C.; Lin H.-I.; CHIN-HSIEN LIN |
| 臺大學術典藏 |
2020-11-03T11:57:07Z |
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.; Lin C.-H.; Chen T.-F.; MING-JANG CHIU; Lin H.-I.; Wu R.-M. |
| 臺大學術典藏 |
2020-09-28T07:04:52Z |
Risk of colorectal cancer in type 2 diabetic patients: A population-based cohort study
|
Chao T.-T.; Wang J.-Y.; Lai C.-C.; Wang C.-Y.; Wang S.-M.; Lin H.-I.; Tang S.-H.; Lin H.-W. |
| 臺大學術典藏 |
2020-08-13T05:24:24Z |
Catheter-related bacteraemia and infective endocarditis caused by Kocuria species
|
Tan C.K.; Lin S.H.; JANN-YUAN WANG; Lai C.C.; Wang C.Y.; Liao C.H.; Chou C.H.; Huang Y.T.; Lin H.I.; Hsueh P.R. |
| 臺大學術典藏 |
2020-08-12T07:46:56Z |
Risk of sepsis among patients with COPD treated with fixed combinations of inhaled corticosteroids and long-acting Beta2 agonists
|
Chen C.-Y.; On the behalf of Taiwan Clinical Trial Consortium for Respiratory Diseases (TCORE); Lai C.-C.; HAO-CHIEN WANG; Chen L.; Yu C.-J.; Yu C.-J.; HAO-CHIEN WANG; Perng D.-W.; Cheng S.-L.; Hsu J.-Y.; Hsu W.-H.; Tsai Y.-H.; Hsiue T.-R.; Lin M.-C.; Lin H.-I.; Wang C.-Y.; Chang Y.-C.; Yang U.-C.; Chen C.-M.; Lin C.-S.; Chen L.; Wei Y.-F.; Chong I.-W.; Wang Y.-H.; Lin Y.S.; Wang C.-Y.; Wang C.-Y.;Lin Y.S.;Wang Y.-H.;Lai C.-C.;Hao-Chien Wang;Chen L.;Yu C.-J.;Yu C.-J.;Hao-Chien Wang;Perng D.-W.;Cheng S.-L.;Hsu J.-Y.;Hsu W.-H.;Tsai Y.-H.;Hsiue T.-R.;Lin M.-C.;Lin H.-I.;Wang C.-Y.;Chang Y.-C.;Yang U.-C.;Chen C.-M.;Lin C.-S.;Chen L.;Wei Y.-F.;Chong I.-W.;Chen C.-Y.;On The Behalf Of Taiwan Clinical Trial Consortium For Respiratory Diseases (Tcore) |
| 臺大學術典藏 |
2020-08-12T06:34:18Z |
Risk of sepsis among patients with COPD treated with fixed combinations of inhaled corticosteroids and long-acting Beta2 agonists
|
Wang C.-Y.; Lin Y.S.; Wang Y.-H.; Lai C.-C.; Wang H.-C.; Chen L.; CHONG-JEN YU; CHONG-JEN YU; Wang H.-C.; Perng D.-W.; Cheng S.-L.; Hsu J.-Y.; Hsu W.-H.; Tsai Y.-H.; Hsiue T.-R.; Lin M.-C.; Lin H.-I.; Wang C.-Y.; Chang Y.-C.; Yang U.-C.; Chen C.-M.; Lin C.-S.; Chen L.; Wei Y.-F.; Chong I.-W.; Chen C.-Y.; On the behalf of Taiwan Clinical Trial Consortium for Respiratory Diseases (TCORE); Wang C.-Y.;Lin Y.S.;Wang Y.-H.;Lai C.-C.;Wang H.-C.;Chen L.;Chong-Jen Yu;Chong-Jen Yu;Wang H.-C.;Perng D.-W.;Cheng S.-L.;Hsu J.-Y.;Hsu W.-H.;Tsai Y.-H.;Hsiue T.-R.;Lin M.-C.;Lin H.-I.;Wang C.-Y.;Chang Y.-C.;Yang U.-C.;Chen C.-M.;Lin C.-S.;Chen L.;Wei Y.-F.;Chong I.-W.;Chen C.-Y.;On The Behalf Of Taiwan Clinical Trial Consortium For Respiratory Diseases (Tcore) |
| 臺大學術典藏 |
2020-07-01T06:19:54Z |
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.;Shu-Hua Yang;Lin H.-I.;Lin C.-H.; Hsueh S.-J.; Lee N.-C.; SHU-HUA YANG; Lin H.-I.; Lin C.-H. |
| 臺大學術典藏 |
2020-04-28T07:25:34Z |
A pathway for tumor necrosis factor-α-induced Bcl10 nuclear translocation: Bcl10 is up-regulated by NF-κB and phosphorylated by Akt1 and then complexes with Bcl3 to enter the nucleus
|
Pei Y.Y.;Kuo S.-H.;Yeh K.-H.;Chuang S.-E.;Chih-Hung Hsu;Wen C.C.;Lin H.-I.;Gao M.;Cheng A.-L.; Pei Y.Y.; Kuo S.-H.; Yeh K.-H.; Chuang S.-E.; CHIH-HUNG HSU; Wen C.C.; Lin H.-I.; Gao M.; Cheng A.-L. |
| 臺大學術典藏 |
2020-04-21T03:52:59Z |
Ultra-high performance flexible piezopotential gated In1-: XSnxSe phototransistor
|
Paul Inbaraj, C. R.; Mathew, R. J.; Haider, G.; Chen, T. P.; Ulaganathan, R. K.; Sankar, R.; Bera, K. P.; Liao, Y. M.; Kataria, M.; Lin, H. I.; Chou, F. C.; Chen, Y. T.; Lee, C. H.; Chen, Y. F. |
| 臺大學術典藏 |
2020-03-27T05:30:04Z |
Infections caused by Gordonia species at a medical centre in Taiwan, 1997 to 2008
|
PO-REN HSUEH; Huang Y.T.; Lin H.I.; Chou C.H.; Liao C.H.; Lin S.H.; Tan C.K.; Liu C.Y.; Wang C.Y.; Lai C.C.; PO-REN HSUEH;Lin H.I.;Huang Y.T.;Chou C.H.;Liao C.H.;Lin S.H.;Tan C.K.;Liu C.Y.;Wang C.Y.;Lai C.C. |
| 臺大學術典藏 |
2020-03-27T05:29:56Z |
Clinical and genotypic characteristics of extensively drug-resistant and multidrug-resistant tuberculosis
|
PO-REN HSUEH; Lin H.I.; Wang C.Y.; Chou C.H.; Hsu H.L.; Liao C.H.; Huang Y.T.; Tan C.K.; Lin S.H.; Lai C.C.; PO-REN HSUEH;Lin H.I.;Wang C.Y.;Hsu H.L.;Chou C.H.;Huang Y.T.;Liao C.H.;Lin S.H.;Tan C.K.;Lai C.C. |
| 臺大學術典藏 |
2020-03-27T05:29:51Z |
Diagnostic value of an enzyme-linked immunospot assay for interferon-γ in genitourinary tuberculosis
|
PO-REN HSUEH;Lin H.-I.;Wang J.-Y.;Wang C.-Y.;Huang Y.-T.;Liao C.-H.;Lin S.-H.;Tan C.-K.;Lai C.-C.; Lai C.-C.; Tan C.-K.; Lin S.-H.; Liao C.-H.; Huang Y.-T.; Wang C.-Y.; Wang J.-Y.; Lin H.-I.; PO-REN HSUEH |
| 臺大學術典藏 |
2020-03-27T05:29:47Z |
Catheter-related bacteraemia and infective endocarditis caused by Kocuria species
|
PO-REN HSUEH; Lin H.I.; Huang Y.T.; Chou C.H.; Liao C.H.; Wang C.Y.; Tan C.K.; Lin S.H.; PO-REN HSUEH;Lin H.I.;Huang Y.T.;Chou C.H.;Liao C.H.;Wang C.Y.;Tan C.K.;Lin S.H.;Wang J.Y.;Lai C.C.; Lai C.C.; Wang J.Y. |
| 臺大學術典藏 |
2020-03-05T01:18:03Z |
Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese population
|
Chen K.-H.; Wu R.-M.; Lin H.-I.; CHUN-HWEI TAI; Lin C.-H. |
| 臺大學術典藏 |
2020-03-05T01:18:02Z |
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.; CHUN-HWEI TAI; Lin H.-I.; Lin C.-H. |
| 臺大學術典藏 |
2020-03-05T01:18:02Z |
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.; CHUN-HWEI TAI; Lin C.-H. |
| 臺大學術典藏 |
2020-03-04T07:45:31Z |
Generation of induced pluripotent stem cells from a patient with Parkinson's disease carrying LRRK2 p.I2012T mutation
|
CHIN-HSIEN LIN; Cheng Y.-C.; Lin H.-I.; Ho M.-C.; Hsu Y.-H.; Wen C.-H.; Ko H.-W.; Lu H.-E.; Huang C.-Y.; Hsieh P.C.H. |
| 臺大學術典藏 |
2020-03-04T07:45:30Z |
Depression and Catechol-O-methyltransferase (COMT) genetic variants are associated with pain in Parkinson's disease
|
Chaudhuri K.R.; Fan J.-Y.; Ko C.-I.; Rizos A.; Chang C.-W.; Lin H.-I.; Wu Y.-R.; CHIN-HSIEN LIN |
| 臺大學術典藏 |
2020-03-04T07:45:30Z |
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 |
| 臺大學術典藏 |
2020-03-04T07:45:30Z |
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. |
| 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 |
| 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. |
