| 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. |
| 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 |
| 臺大學術典藏 |
2020-02-25T08:01:16Z |
PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population
|
Fan T.-S;Ruey-Meei Wu;Lin H.-I;Cheng C;Lin C.-H.; Fan T.-S; RUEY-MEEI WU; Lin H.-I; Cheng C; Lin C.-H. |
| 臺大學術典藏 |
2020-01-13T08:21:34Z |
Real-time 3-D feature detection and correspondence refinement for indoor environment-mapping using RGB-D cameras
|
Chen, L.-C.; Van Thai, N.; Lin, H.-I.; LIANG-CHIA CHEN |
| 臺大學術典藏 |
2020-01-13T08:21:33Z |
In situ clouds-powered 3-D radiation detection and localization using novel color-depth-radiation (CDR) mapping
|
Chen, L.-C.; Van Thai, N.; Shyu, H.-F.; Lin, H.-I.; LIANG-CHIA CHEN |
| 臺大學術典藏 |
2020-01-13T08:21:30Z |
Development of Registration methodology to 3-D Point Clouds in Robot Scanning
|
Chen, L.-C.; Hoang, D.-C.; Chu, T.-T.; Lin, H.-I.; LIANG-CHIA CHEN |
| 臺大學術典藏 |
2020-01-13T08:21:30Z |
A 3-D point clouds scanning and registration methodology for automatic object digitization
|
Nguyen, T.-H.; LIANG-CHIA CHEN; Hoang, D.-C.; Lin, H.-I.; Chen, L.-C. |
