| 臺大學術典藏 |
2021-09-23T03:48:58Z |
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy
|
Lin C.-H.; Tsai P.-.; Lin H.-Y.; Hattori N.; Funayama M.; Jeon B.; Sato K.; Abe K.; Mukai Y.; Takahashi Y.; Li Y.; Nishioka K.; Yoshino H.; Daida K.; Chen M.-L.; Cheng J.; Huang C.-Y.; Tzeng S.-R.; Wu Y.-S.; Lai H.-J.; Tsai H.-H.; Yen R.-F.; Lee N.-C.; Lo W.-C.; Hung Y.-C.; Chan C.-C.; Ke Y.-C.; CHI-CHAO CHAO; Hsieh S.-T.; Farrer M.; Wu R.-M. |
| 臺大學術典藏 |
2021-09-01T01:54:14Z |
O6-Methylguanine-DNA methyltransferase expression and prognostic value in brain metastases of lung cancers
|
Wu P.-F.; Kuo K.-T.; Kuo L.-T.; Lin Y.-T.; Lee W.-C.; Lu Y.-S.; Yang C.-H.; Wu R.-M.; Tu Y.-K.; Tasi J.-C.; Tseng H.-M.; Tseng S.-H.; ANN-LII CHENG; Lin C.-H. |
| 臺大學術典藏 |
2021-07-06T02:04:04Z |
Clinical heterogeneity of LRRK2 p.I2012T mutation
|
Fan T.-S.;Wu R.-M.;Pei-Lung Chen;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.; Wu R.-M.; PEI-LUNG CHEN; 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 |
2021-07-06T02:03:54Z |
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.;Pei-Lung Chen;Tai C.-H.;Lin H.-I.;Chen C.-S.;Chen M.-L.;Wu R.-M.; Lin C.-H.; PEI-LUNG CHEN; Tai C.-H.; Lin H.-I.; Chen C.-S.; Chen M.-L.; Wu R.-M. |
| 臺大學術典藏 |
2021-06-01T07:03:25Z |
Overexpression of heme oxygenase-1 protects dopaminergic neurons against 1-methyl-4-phenylpyridinium-induced neurotoxicity
|
Hung S.-Y.; Liou H.-C.; Kang K.-H.; Wu R.-M.; Wen C.-C.; WEN-MEI FU |
| 臺大學術典藏 |
2021-06-01T07:03:19Z |
Increase of oxidative stress by a novel PINK1 mutation, P209A
|
Chien W.-L.; Lee T.-R.; Hung S.-Y.; Kang K.-H.; Wu R.-M.; Lee M.-J.; WEN-MEI FU |
| 臺大學術典藏 |
2021-05-26T03:35:59Z |
Current role of surgery in the management of pleuropulmonary tuberculosis.
|
Lee Y.C.; Luh S.P.; Wu R.M.; Lin T.P.; KWEN-TAY LUH |
| 臺大學術典藏 |
2021-04-29T02:21:10Z |
Mystery Case: Hemiballism in a patient with parietal lobe infarction
|
MENG-CHEN WU; Yen R.-F.; Lin C.-H.; Wu R.-M.; Nita D.A. |
| 臺大學術典藏 |
2021-03-18T05:59:14Z |
Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism
|
Lee M.-J.; Mata I.F.; Lin C.-H.; KAI-YUAN TZEN; Lincoln S.J.; Bounds R.; Lockhart P.J.; Hulihan M.M.; Farrer M.J.; Wu R.-M. |
| 臺大學術典藏 |
2021-03-18T05:59:14Z |
LRRK2 mutation in familial Parkinson's disease in a Taiwanese population: Clinical, PET, and functional studies
|
Lin C.-H.; KAI-YUAN TZEN; Yu C.-Y.; Tai C.-H.; Farrer M.J.; Wu R.-M. |
| 臺大學術典藏 |
2021-03-18T05:59:08Z |
Gene therapy for aromatic L-amino acid decarboxylase deficiency
|
Hwu W.-L.; Muramatsu S.-I.; Tseng S.-H.; KAI-YUAN TZEN; Lee N.-C.; Chien Y.-H.; Snyder R.O.; Byrne B.J.; Tai C.-H.; Wu R.-M. |
| 臺大學術典藏 |
2021-03-18T05:59:05Z |
Dopaminergic Neuronal Imaging in Genetic Parkinson's Disease: Insights into Pathogenesis
|
McNeill A.; Wu R.-M.; KAI-YUAN TZEN; Aguiar P.C.; Arbelo J.M.; Barone P.; Bhatia K.; Barsottini O.; Bonifati V.; Bostantjopoulou S.; Bressan R.; Cossu G.; Cortelli P.; Felicio A.; Ferraz H.B.; Herrera J.; Houlden H.; Hoexter M.; Isla C.; Lees A.; Lorenzo-Betancor O.; Mencacci N.E.; Pastor P.; Pappata S.; Pellecchia M.T.; Silveria-Moriyama L.; Varrone A.; Foltynie T.; Schapira A.H.V. |
| 臺大學術典藏 |
2021-03-12T07:59:00Z |
The COMT L allele modifies the association between MAOB polymorphism and PD in Taiwanese
|
Kai Hsiang Stanley Chen; Wu, R.M.; Cheng, C.W.; Lu, S.L.; Shan, D.E.; Ho, Y.F.; Chern, H.D. |
| 臺大學術典藏 |
2021-03-12T07:59:00Z |
Genetic polymorphism of the CYP2E1 gene and susceptibility to Parkinson's disease in Taiwanese
|
Kai Hsiang Stanley Chen; Wu, R.M.; Cheng, C.W.; Chen, K.H.; Shan, D.E.; Kuo, J.W.; Ho, Y.F.; Chern, H.D. |
| 臺大學術典藏 |
2021-03-08T08:06:09Z |
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy
|
Lin C.-H.; Tsai P.-.; Lin H.-Y.; Hattori N.; Funayama M.; Jeon B.; Sato K.; Abe K.; Mukai Y.; Takahashi Y.; Li Y.; Nishioka K.; Yoshino H.; Daida K.; Chen M.-L.; Cheng J.; Huang C.-Y.; Tzeng S.-R.; Wu Y.-S.; Lai H.-J.; Tsai H.-H.; Yen R.-F.; Lee N.-C.; Lo W.-C.; Hung Y.-C.; Chan C.-C.; Ke Y.-C.; Chao C.-C.; SUNG-TSANG HSIEH; Farrer M.; Wu R.-M. |
| 臺大學術典藏 |
2021-03-08T06:51:46Z |
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy
|
Lin C.-H.; Tsai P.-.; Lin H.-Y.; Hattori N.; Funayama M.; Jeon B.; Sato K.; Abe K.; Mukai Y.; Takahashi Y.; Li Y.; Nishioka K.; Yoshino H.; Daida K.; Chen M.-L.; Cheng J.; Huang C.-Y.; Tzeng S.-R.; Wu Y.-S.; Lai H.-J.; Tsai H.-H.; Yen R.-F.; Lee N.-C.; Lo W.-C.; Hung Y.-C.; CHIH-CHIANG CHAN; Ke Y.-C.; Chao C.-C.; Hsieh S.-T.; Farrer M.; Wu R.-M. |
| 國立成功大學 |
2021 |
Interactions of comt and aldh2 genetic polymorphisms on symptoms of parkinson’s disease
|
Yu, R.-L.;Tu, S.-C.;Wu, R.-M.;Lu, P.-A.;Tan, C.-H. |
| 臺大學術典藏 |
2020-12-24T06:16:51Z |
Gene therapy for aromatic L-amino acid decarboxylase deficiency
|
Wu R.-M.; Tai C.-H.; Byrne B.J.; YIN-HSIU CHIEN; Snyder R.O.; Lee N.-C.; Tzen K.-Y.; Tseng S.-H.; Muramatsu S.-I.; Hwu W.-L. |
| 臺大學術典藏 |
2020-12-23T02:57:44Z |
Restless legs syndrome in end-stage renal disease: A multicenter study in Taiwan
|
Wu R.-M.; Chen Y.-M.; Lin S.-Y.; Wu K.-D.; Chang H.-W.; Lin C.-Y.; Lion H.-H.; Chiu P.-F.; Chang C.-C.; Wu S.-L.; Sy H.-N.; Li W.-Y.; VIN-CENT WU; Lin C.-H.;Vin-Cent Wu;Li W.-Y.;Sy H.-N.;Wu S.-L.;Chang C.-C.;Chiu P.-F.;Lion H.-H.;Lin C.-Y.;Chang H.-W.;Lin S.-Y.;Wu K.-D.;Chen Y.-M.;Wu R.-M.; Lin C.-H. |
| 臺大學術典藏 |
2020-12-23T02:57:34Z |
Restless legs syndrome is associated with cardio/cerebrovascular events and mortality in end-stage renal disease
|
Lin C.-H.; Sy H.-N.; Chang H.-W.; Liou H.-H.; Lin C.-Y.; VIN-CENT WU; Wu S.-L.; Chang C.-C.; Chiu P.-F.; Li W.-Y.; Lin S.-Y.; Wu K.-D.; Chen Y.-M.; Wu R.-M. |
| 臺大學術典藏 |
2020-12-18T02:21:51Z |
Plasma calcitonin gene-related peptide in diagnosing and predicting paediatric migraine
|
Fan P.-C.;Kuo P.-H.;Chang S.-H.;Wang-Tso Lee;Wu R.-M.;Chiou L.-C.; Fan P.-C.; Kuo P.-H.; Chang S.-H.; WANG-TSO LEE; Wu R.-M.; Chiou L.-C. |
| 臺大學術典藏 |
2020-12-16T02:26:19Z |
Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and Parkin gene mutations
|
Wu R.-M.;Shan D.-E.;Sun C.-M.;Liu R.-S.;Wuh-Liang Hwu;Tai C.-H.;Hussey J.;West A.;Gwinn-Hardy K.;Hardy J.;Chen J.;Farrer M.;Lincoln S.; Wu R.-M.; Shan D.-E.; Sun C.-M.; Liu R.-S.; WUH-LIANG HWU; Tai C.-H.; Hussey J.; West A.; Gwinn-Hardy K.; Hardy J.; Chen J.; Farrer M.; Lincoln S. |
| 臺大學術典藏 |
2020-12-16T02:26:10Z |
DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients
|
Wang C.K.;Wu Y.R.;Wuh-Liang Hwu;Chen C.M.;Ro L.S.;Chen S.T.;Gwinn-Hardy K.;Yang C.C.;Wu R.M.;Chen T.F.;Wang H.C.;Chao M.C.;Chiu M.J.;Lu C.J.;Lee-Chen G.J.; Wang C.K.; Wu Y.R.; WUH-LIANG HWU; Chen C.M.; Ro L.S.; Chen S.T.; Gwinn-Hardy K.; Yang C.C.; Wu R.M.; Chen T.F.; Wang H.C.; Chao M.C.; Chiu M.J.; Lu C.J.; Lee-Chen G.J. |
| 臺大學術典藏 |
2020-12-16T02:26:09Z |
Parkin mutations and early-onset parkinsonism in a Taiwanese cohort
|
Wu R.-M.;Bounds R.;Lincoln S.;Hulihan M.;Lin C.-H.;Wuh-Liang Hwu;Chen J.;Gwinn-Hardy K.;Farrer M.; Wu R.-M.; Bounds R.; Lincoln S.; Hulihan M.; Lin C.-H.; WUH-LIANG HWU; Chen J.; Gwinn-Hardy K.; Farrer M. |
| 臺大學術典藏 |
2020-12-16T02:26:00Z |
Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (Ethnic Chinese) cohort of familial and early-onset parkinsonism
|
Lin C.-H.;Wuh-Liang Hwu;Chiang S.-C.;Tai C.-H.;Wu R.-M.; Lin C.-H.; WUH-LIANG HWU; Chiang S.-C.; Tai C.-H.; Wu R.-M. |
