| 臺大學術典藏 |
2020-11-03T11:45:23Z |
Hereditary neuropathy with liability to pressure palsies: A clinical and electrophysiological study
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Cheng M.-L.;Jiann-Shing Jeng;Sung S.-F.;Chang Y.-C.;Huang C.-C.;Chen R.- C.;Hsieh S.-T.; Cheng M.-L.; JIANN-SHING JENG; Sung S.-F.; Chang Y.-C.; Huang C.-C.; Chen R.- C.; Hsieh S.-T. |
| 國立臺灣大學 |
1991 |
Hereditary Pancreatitis in a Chinese Family
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林肇堂; Wang, T. H.; 陳定信; Lin, Jaw-Town; Wang, T. H.; Chen, Ding-Shinn |
| 國立臺灣大學 |
1994 |
Hereditary Progressive Dystonia with Marked Diurnal Fluctuation (Segawa Syndrome) in Taiwan
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王本榮; 楊千立; 胡務亮; 沈友仁; WANG, PEN-JUNG; KO, YOU-MIN; YOUNG, CHAINLLIE; HWU, WUH-LIANG; SHEN, YU-ZEN |
| 臺大學術典藏 |
2020-12-16T02:26:30Z |
Hereditary progressive dystonia with marked diurnal fluctuation (Segawa syndrome) in Taiwan
|
Wang P.-J.; Ko Y.-M.; Young C.; WUH-LIANG HWU; Shen Y.-Z. |
| 臺大學術典藏 |
2020-12-16T02:26:33Z |
Hereditary progressive dystonia with marked diurnal fluctuation: report of a case.
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WUH-LIANG HWU; Wang P.J.; Shen Y.Z. |
| 國立臺灣大學 |
1989 |
Hereditary Progressive Dystonia with Marked Diurnal Fluctuation:Report of A Case
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王本榮; Shen, Y. Z.; 胡務亮; Wang, Pen-Jung; Shen, Y. Z.; Hwu, Wuh-Liang |
| 國立臺灣大學 |
1989 |
Hereditary Progrressive Dystonia with Marked Diurnal Fluctuation, Report of a Case
|
胡務亮; Wang, P. J.; Shen, Y. Z.; Hwu, Wuh-Liang; Wang, P. J.; Shen, Y. Z. |
| 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
|
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 |
2020-03-03T02:33:36Z |
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) gene
|
MING-JEN LEE; Stephenson D.A.; Groves M.J.; Sweeney M.G.; Davis M.B.; An S.-F.; Houlden H.; Salih M.A.M.; Timmerman V.; de Jonghe P.; Auer-Grumbach M.; Di Maria E.; Scaravilli F.; Wood N.W.; Reilly M.M. |
| 臺大學術典藏 |
2020-11-03T11:32:32Z |
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) gene
|
Houlden H.; Salih M.A.M.; Timmerman V.; de Jonghe P.; Auer-Grumbach M.; Di Maria E.; Scaravilli F.; Wood N.W.; Reilly M.M.; Davis M.B.; An S.-F.; Sweeney M.G.; Groves M.J.; Stephenson D.A.; MING-JEN LEE |
