|
English
|
正體中文
|
简体中文
|
Total items :0
|
|
Visitors :
51362287
Online Users :
1130
Project Commissioned by the Ministry of Education
Project Executed by National Taiwan University Library
|
|
|
|
Taiwan Academic Institutional Repository >
Browse by Author
|
"wu r m"
Showing items 36-45 of 414 (42 Page(s) Totally)
<< < 1 2 3 4 5 6 7 8 9 10 > >>
View [10|25|50] records per page
| 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. |
Showing items 36-45 of 414 (42 Page(s) Totally)
<< < 1 2 3 4 5 6 7 8 9 10 > >>
View [10|25|50] records per page
|
