| 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. |
| 臺大學術典藏 |
2020-12-16T02:25:36Z |
Gene therapy for aromatic L-amino acid decarboxylase deficiency
|
WUH-LIANG HWU; Muramatsu S.-I.; Tseng S.-H.; Tzen K.-Y.; Lee N.-C.; Chien Y.-H.; Snyder R.O.; Byrne B.J.; Tai C.-H.; Wu R.-M. |
| 臺大學術典藏 |
2020-12-16T02:25:00Z |
Modified frameless stereotactic system for intracerebral delivery of viral vector in young children
|
Tai C.-H.;Wuh-Liang Hwu;Wu R.-M.;Tseng S.-H.; Tai C.-H.; WUH-LIANG HWU; Wu R.-M.; Tseng S.-H. |
| 臺大學術典藏 |
2020-12-09T01:38:31Z |
Gene therapy for aromatic L-amino acid decarboxylase deficiency
|
Hwu W.-L.; Muramatsu S.-I.; Tseng S.-H.; Tzen K.-Y.; NI-CHUNG LEE; Chien Y.-H.; Snyder R.O.; Byrne B.J.; Tai C.-H.; Wu R.-M. |
| 臺大學術典藏 |
2020-12-02T02:36:00Z |
Small-cell lung cancer presenting with Lambert-Eaton myasthenic syndrome and respiratory failure
|
Jiang J.-R.;Shih J.-Y.;Wang H.-C.;Wu R.-M.;Yu C.-J.;Pan-Chyr Yang; Jiang J.-R.; Shih J.-Y.; Wang H.-C.; Wu R.-M.; Yu C.-J.; PAN-CHYR YANG |
| 臺大學術典藏 |
2020-11-03T12:21:56Z |
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.;Hwu W.-L.;Chun-Hwei Tai;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.; Hwu W.-L.; CHUN-HWEI TAI; Hussey J.; West A.; Gwinn-Hardy K.; Hardy J.; Chen J.; Farrer M.; Lincoln S. |
| 臺大學術典藏 |
2020-11-03T12:21:54Z |
Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation
|
CHUN-HWEI TAI; Yen R.-F.; Lin C.-H.; Yen K.-Y.; Yip P.-K.; Wu R.-M.; Lee M.-J. |
| 臺大學術典藏 |
2020-11-03T12:21:53Z |
Feeling-of-knowing in episodic memory in patients with Parkinson's disease with various motor symptoms
|
Yu R.-L.; Wu R.-M.; CHUN-HWEI TAI; Lin C.-H.; Hua M.-S.; Yu R.-L.;Wu R.-M.;Chun-Hwei Tai;Lin C.-H.;Hua M.-S. |
| 臺大學術典藏 |
2020-11-03T12:21:52Z |
Meige syndrome relieved by bilateral pallidal stimulation with cycling mode: Case report
|
Wu R.-M.; Liu H.-M.; Tsai C.-W.; Tseng S.-H.; Chun-Hwei Tai;Wu R.-M.;Liu H.-M.;Tsai C.-W.;Tseng S.-H.; CHUN-HWEI TAI |
| 臺大學術典藏 |
2020-11-03T12:21:52Z |
Lrrk2 S1647T and BDNF V66M interact with environmental factors to increase risk of Parkinson's disease
|
Lin C.-H.; Wu R.-M.; CHUN-HWEI TAI; Chen M.-L.; Hu F.-C.; Lin C.-H.;Wu R.-M.;Chun-Hwei Tai;Chen M.-L.;Hu F.-C. |
| 臺大學術典藏 |
2020-11-03T12:21:51Z |
Neuropsychological profile in patients with early stage of Parkinson's disease in Taiwan
|
Hua M.-S.; Cheng T.-W.; Lin C.-H.; CHUN-HWEI TAI; Wu R.-M.; Yu R.-L. |
