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Showing items 116-123 of 123 (13 Page(s) Totally)
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| 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 116-123 of 123 (13 Page(s) Totally)
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