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"ming jen lee"
Showing items 96-123 of 123 (3 Page(s) Totally)
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| 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 |
| 臺大學術典藏 |
2018-09-10T05:12:07Z |
Complex haplotypic effects of the ABCB1 gene on epilepsy treatment response
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Hung, C.-C.;Tai, J.J.;Lin, C.-J.;Lee, M.-J.;Liou, H.-H.; Horng-Huei Liou; CHUN-JUNG LIN; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T05:01:23Z |
Cutaneous and sympathetic denervation in neonatal rats with a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 gene
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Hsu, S.-H. and Lee, M.-J. and Hsieh, S.-C. and Scaravilli, F. and Hsieh, S.-T.; SHU-HAO HSU; SUNG-TSANG HSIEH; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T04:25:34Z |
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) gene
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Lee, M.-J. and Stephenson, D.A. and Groves, M.J. and Sweeney, M.G. and Davis, M.B. and An, S.-F. and Houlden, H. and Salih, M.A.M. and Timmerman, V. and de Jonghe, P. and Auer-Grumbach, M. and Di Maria, E. and Scaravilli, F. and Wood, N.W. and Reilly, M.M.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T04:05:42Z |
Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis [4]
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Lee, M.-J. and Huang, Y.-C. and Sweeney, M.G. and Wood, N.W. and Reilly, M.M. and Yip, P.-K.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T04:05:42Z |
Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth disease
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Lee, M.-J. and Nelson, I. and Houlden, H. and Sweeney, M.G. and Hilton-Jones, D. and Blake, J. and Wood, N.W. and Reilly, M.M.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T03:41:56Z |
Biochemical events coupled to the activation of serotonin receptors in brain regions of the rat
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Wei, J.-W. and Lee, M.-J. and Yeh, S.-R.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T03:24:14Z |
Genetic aspects of hereditary motor and sensory neuropathy
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Lee, M.-J. and Reilly, M.M.; MING-JEN LEE |
| 中國醫藥大學 |
2013-05 |
Increase of oxidative stress by a novel PINK1 mutation, P209A.
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(Wei-Lin Chien);(Tzeng-Ruei Lee);洪詩雅(Shih-Ya Hung);(Kai-Hsiang Kang);(Ruey-Meei Wu);(Ming-Jen Lee);(Wen-Mei Fu)* |
| 中國醫藥大學 |
2009-09 |
Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation
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(Chun-Hwei Tai);顏若芳(Ruoh-Fan Yen);(Chin-Hsien Lin);顏國揚(Kuo-Yang Yen);(Ping-Keung Yip);(Ruey-Meei Wu);(Ming-Jen Lee)* |
| 臺大學術典藏 |
2006 |
Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke
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Yip P.-K.; Jeng J.-S.; MING-JEN LEE; Tang S.-C. |
| 臺大學術典藏 |
2005 |
Six novel NPC1 mutations in Chinese patients with Niemann-Pick disease type C
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Yang, C.-C. and Su, Y.-N. and Chiou, P.-C. and Fietz, M.J. and Yu, C.-L. and Hwu, W.-L. and Lee, M.-J.; MING-JEN LEE; WUH-LIANG HWU; Chih-Chao Yang |
| 臺大學術典藏 |
2005 |
Complex haplotypic effects of the ABCB1 gene on epilepsy treatment response
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Liou H.-H.; MING-JEN LEE; Lin C.-J.; Tai J.J.; Hung C.-C. |
| 臺大學術典藏 |
2002 |
Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis [4]
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Yip P.-K.; Reilly M.M.; Wood N.W.; Sweeney M.G.; Huang Y.-C.; MING-JEN LEE |
Showing items 96-123 of 123 (3 Page(s) Totally)
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