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"ming jen lee"的相关文件
显示项目 101-110 / 123 (共13页)
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| 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 |
显示项目 101-110 / 123 (共13页)
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