| 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. |
