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Taiwan Academic Institutional Repository >
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"ming jen lee"
Showing items 106-115 of 123 (13 Page(s) Totally)
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| 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 |
Showing items 106-115 of 123 (13 Page(s) Totally)
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