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"ming jen lee"的相關文件
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| 臺大學術典藏 |
2018-09-10T09:14:42Z |
PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort
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Lee, Y.-C. and Lee, M.-J. and Yu, H.-Y. and Chen, C. and Hsu, C.-H. and Lin, K.-P. and Liao, K.-K. and Chang, M.-H. and Liao, Y.-C. and Soong, B.-W.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T09:14:42Z |
The systems biology of neurofibromatosis type 1 - Critical roles for microRNA
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Lee, Ming-Jen;Cho, Ji-Hoon;Galas, David J.;Wang, Kai; Lee, M.-J. and Cho, J.-H. and Galas, D.J. and Wang, K.; 李銘仁; Lee, Ming-Jen; Hsu, Wei-Hsuan; MING-JEN LEE; Lee, Bao-Hong; Cho, Ji-Hoon; Pan, Tzu-Ming; Galas, David J.; Wang, Kai |
| 臺大學術典藏 |
2018-09-10T08:30:52Z |
Clinical phenotype of G206D mutation in the presenilin 1 gene in pathologically confirmed familial Alzheimer's disease
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Wu, Y.-Y. and Cheng, I.H.-J. and Lee, C.-C. and Chiu, M.-J. and Lee, M.-J. and Chen, T.-F. and Hsu, J.-L.; Ta-Fu Chen; Ming-Jang Chiu; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T08:30:51Z |
Neurological complications of acute intermittent porphyria
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Kuo, H.-C. and Huang, C.-C. and Chu, C.-C. and Lee, M.-J. and Chuang, W.-L. and Wu, C.-L. and Wu, T. and Ning, H.-C. and Liu, C.-Y.; 郭弘周;黃錦章;朱俊哲;李銘仁;莊雯莉;吳東霖;甯孝真;劉智仰; KUO, HUNG-CHOU;HUANG, CHIN-CHANG;CHU, CHUN-CHE;LEE, MING-JEN;CHUANG, WEN-LI;WU, TONY T.;NING, HSIAO-CHEN;LIU, CHIH-YANG; MING-JEN LEE; Rand, D; Eng, JJ; Tang, PF; Jeng, JS; Hung, C; KUO, HUNG-CHOU; HUANG, CHIN-CHANG; CHU, CHUN-CHE; LEE, MING-JEN; CHUANG, WEN-LI; WU, TONY T.; NING, HSIAO-CHEN; LIU, CHIH-YANG |
| 臺大學術典藏 |
2018-09-10T08:30:51Z |
Purple pigments: The pathophysiology of acute porphyric neuropathy
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Lin, C.S.-Y. and Lee, M.-J. and Park, S.B. and Kiernan, M.C.; 李銘仁; Lin, Cindy S.-Y.; Lee, Ming-Jen; Park, Susanna B.; Kiernan, Matthew C.; MING-JEN LEE; Lin, Cindy S.-Y.; Lee, Ming-Jen; Park, Susanna B.; Kiernan, Matthew C. |
| 臺大學術典藏 |
2018-09-10T08:30:51Z |
rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese population
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Lee, M.-J. and Chen, T.-F. and Cheng, T.-W. and Chiu, M.-J.; Lee, Ming-Jen;Chen, Ta-Fu;Cheng, Ting-Wen;Chiu, Ming-Jang; Lee, Ming-Jen; Ta-Fu Chen; Chen, Ta-Fu; MING-JEN LEE; Cheng, Ting-Wen; Ming-Jang Chiu; Chiu, Ming-Jang |
| 臺大學術典藏 |
2018-09-10T08:30:51Z |
Valosin-containing protein and neurofibromin interact to regulate dendritic spine density
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Wang, H.-F. and Shih, Y.-T. and Chen, C.-Y. and Chao, H.-W. and Lee, M.-J. and Hsueh, Y.-P.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T08:04:48Z |
Cerebral amyloid angiopathy in East and West
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陳右緯;李銘仁; Chen, Y.-W. and Lee, M.-J. and Smith, E.E.; Chen, Yu-Wei; Lee, Ming-Jen; Smith, Eric E.; MING-JEN LEE; Chen, Yu-Wei; Lee, Ming-Jen; Smith, Eric E. |
| 臺大學術典藏 |
2018-09-10T08:04:48Z |
Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser
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Yang, N.C.-C. and Lee, M.-J. and Chao, C.-C. and Chuang, Y.-T. and Lin, W.-M. and Chang, M.-F. and Hsieh, P.-C. and Kan, H.-W. and Lin, Y.-H. and Yang, C.-C. and Chiu, M.-J. and Liou, H.-H. and Hsieh, S.-T.; CHI-CHAO CHAO; Horng-Huei Liou; SUNG-TSANG HSIEH; Ming-Jang Chiu; MING-JEN LEE; Chih-Chao Yang |
| 臺大學術典藏 |
2018-09-10T08:03:51Z |
The microRNA spectrum in 12 body fluids
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Weber, J.A. and Baxter, D.H. and Zhang, S. and Huang, D.Y. and Huang, K.H. and Lee, M.J. and Galas, D.J. and Wang, K.; KUO-HOW HUANG; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T07:32:11Z |
Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism
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Lee, M.-J. and Mata, I.F. and Lin, C.-H. and Tzen, K.-Y. and Lincoln, S.J. and Bounds, R. and Lockhart, P.J. and Hulihan, M.M. and Farrer, M.J. and Wu, R.-M.; 李銘仁;林靜嫻;曾凱元;吳瑞美; Lee, Ming-Jen; Mata, Ignacio F.; Lin, Chin-Hsien; Tzen, Kai-Yuan; Lincoln, Sarah J.; Bounds, Rebecca; Lockhart, Paul J.; Hulihan, Mary M.; Farrer, Matthew J.; Wu, Ruey-Meei; Ruey-Meei Wu; Chin-Hsien Lin; KAI-YUAN TZEN; MING-JEN LEE; Lee, Ming-Jen; Mata, Ignacio F.; Lin, Chin-Hsien; Tzen, Kai-Yuan; Lincoln, Sarah J.; Bounds, Rebecca; Lockhart, Paul J.; Hulihan, Mary M.; Farrer, Matthew J.; Wu, Ruey-Meei |
| 臺大學術典藏 |
2018-09-10T07:22:49Z |
Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation
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Tai, Chun-Hwei;Yen, Ruoh-Fan;Lin, Chin-Hsien;Yen, Kuo-Yang;Yip, Ping-Keung;Wu, Ruey-Meei;Lee, Ming-Jen; Tai, C.-H. and Yen, R.-F. and Lin, C.-H. and Yen, K.-Y. and Yip, P.-K. and Wu, R.-M. and Lee, M.-J.; Tai, Chun-Hwei; Ruey-Meei Wu; CHUN-HWEI TAI; Yen, Ruoh-Fan; Lin, Chin-Hsien; RUOH-FANG YEN; Chin-Hsien Lin; Yen, Kuo-Yang; Yip, Ping-Keung; MING-JEN LEE; Wu, Ruey-Meei; Lee, Ming-Jen |
| 臺大學術典藏 |
2018-09-10T07:22:27Z |
Longitudinal evaluation of an N-Ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus
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李銘仁;陳燕惠;郭律廷;陳垣崇;洪舜郁;鄔哲源;張程; Lee, M.-J. and Chang, C.-P. and Lee, Y.-H. and Wu, Y.-C. and Tseng, H.-W. and Tung, Y.-Y. and Wu, M.-T. and Chen, Y.-H. and Kuo, L.-T. and Stephenson, D. and Hung, S.-L. and Wu, J.-Y. and Chang, C. and Chen, Y.-T. and Chern, Y.; Lee, Ming-Jen; Chang, Ching-Pang; Lee, Yi-Hsin; Wu, Yi-Chih; Tseng, Hsu-Wen; Tung, Yu-Ying; Wu, Min-Tzu; Chen, Yen-Hui; Kuo, Lu-Ting; Stephenson, Dennis; Hung, Shuen-Iu; Wu, Jer-Yuarn; Chang, Chen; Chen, Yuan-Tsong; Chern, Yijuang; ���P�f; Lu-Ting Kuo; MING-JEN LEE; Lee, Ming-Jen; Chang, Ching-Pang; Lee, Yi-Hsin; Wu, Yi-Chih; Tseng, Hsu-Wen; Tung, Yu-Ying; Wu, Min-Tzu; Chen, Yen-Hui; Kuo, Lu-Ting; Stephenson, Dennis; Hung, Shuen-Iu; Wu, Jer-Yuarn; Chang, Chen; Chen, Yuan-Tsong; Chern, Yijuang |
| 臺大學術典藏 |
2018-09-10T07:22:27Z |
Notch signaling and CADASIL
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Tang, S.-C. and Jeng, J.-S. and Lee, M.-J. and Yip, P.-K.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T07:11:38Z |
Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese
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Chen, S.-R. and Lin, K.-P. and Kuo, H.-C. and Chen, C.-M. and Hsieh, S.-T. and Lee, M.-J. and Yang, C.-C. and Liu, C.-S. and Huang, C.-C. and Lyu, R.-K. and Ro, L.-S.; SUNG-TSANG HSIEH; MING-JEN LEE; Chih-Chao Yang |
| 臺大學術典藏 |
2018-09-10T06:50:20Z |
HMBS mutations in chinese patients with acute intermittent porphyria
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Yang, C.-C.;Kuo, H.-C.;You, H.-L.;Wang, J.;Huang, C.-C.;Liu, C.-Y.;Lan, M.-Y.;Stephenson, D.A.;Lee, M.-J.; MING-JEN LEE; Chih-Chao Yang |
| 臺大學術典藏 |
2018-09-10T06:50:20Z |
Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum
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李銘仁;鄭婷文;花茂棽;潘明楷;楊智超; Lee, M-J; Cheng, T-W; Hua, M-S; Pan, M-K; Wang, J; Stephenson, D A; Yang, C-C; Lee, M.-J. and Cheng, T.-W. and Hua, M.-S. and Pan, M.-K. and Wang, J. and Stephenson, D.A. and Yang, C.-C.; LEE, MING-JEN;CHENG, TING-WEN;HUA, MAU- SUN;PAN, MING-KAI;YANG, CHIH-CHAO; Lee, M-J; Ming-Kai Pan; MING-JEN LEE; Cheng, T-W; Chih-Chao Yang; Hua, M-S; Pan, M-K; Wang, J; LEE, MING-JEN; Stephenson, D A; Yang, C-C; CHENG, TING-WEN; HUA, MAU- SUN; PAN, MING-KAI; YANG, CHIH-CHAO |
| 臺大學術典藏 |
2018-09-10T06:50:20Z |
Nerve function and dysfunction in acute intermittent porphyria
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Lin, C.S.-Y. and Krishnan, A.V. and Lee, M.-J. and Zagami, A.S. and You, H.-L. and Yang, C.-C. and Bostock, H. and Kiernan, M.C.; 李銘仁;楊智超; Lin, C. S.-Y.; Krishnan, A. V.; Lee, M.-J.; Zagami, A. S.; You, H.-L.; Yang, C.-C.; Bostock, H.; Kiernan, M. C.; MING-JEN LEE; Chih-Chao Yang; Lin, C. S.-Y.; Krishnan, A. V.; Lee, M.-J.; Zagami, A. S.; You, H.-L.; Yang, C.-C.; Bostock, H.; Kiernan, M. C. |
| 臺大學術典藏 |
2018-09-10T06:40:07Z |
Characterization of a familial case with primary erythromelalgia from Taiwan
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Lee, M.-J.;Yu, H.-S.;Hsieh, S.-T.;Stephenson, D.A.;Lu, C.-J.;Yang, C.-C.; SUNG-TSANG HSIEH; MING-JEN LEE; Chih-Chao Yang |
| 臺大學術典藏 |
2018-09-10T06:15:01Z |
Acute intermittent porphyria with peripheral neuropathy: A follow-up study after hematin treatment
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Kuo, H.-C. and Lee, M.-J. and Chuang, W.-L. and Huang, C.-C.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T06:15:01Z |
Recent developments in neurofibromatosis type 1
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Lee, M.-J. and Stephenson, D.A.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T06:15:01Z |
Clinical and electrophysiological characteristics of inflammatory demyelinating neuropathies
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Lee, M.-J. and Chang, Y.-C. and Chen, R.-C. and Hsieh, S.-T.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T05:46:48Z |
Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1.
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Lee, M.J. and Su, Y.N. and You, H.L. and Chiou, S.C. and Lin, L.C. and Yang, C.C. and Lee, W.C. and Hwu, W.L. and Hsieh, F.J. and Stephenson, D.A. and Yu, C.L.; MING-JEN LEE; WUH-LIANG HWU; Chih-Chao Yang |
| 臺大學術典藏 |
2018-09-10T05:46:48Z |
Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke
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Tang, S.-C. and Lee, M.-J. and Jeng, J.-S. and Yip, P.-K.; JIANN-SHING JENG; MING-JEN LEE; Sung-Chun Tang |
| 臺大學術典藏 |
2018-09-10T05:12:36Z |
Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
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Tang, S.-C. and Lee, M.-J. and Jeng, J.-S. and Yip, P.-K.; JIANN-SHING JENG; MING-JEN LEE; Sung-Chun Tang |
顯示項目 86-110 / 123 (共5頁)
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