| 臺大學術典藏 |
2016 |
Hereditary Genius in the Grandeur of Life: The New Man, the Beast Man and the Crazy Scientist on Dr. Moreau’s Island
|
CHUNG-JEN CHEN |
| 臺北醫學大學 |
1999 |
Hereditary gingival fibromatosis and its three generations pedigree-- case report
|
項家蘭; 郭倍榮; Chia-Lan Hsiang Bey-Rong Guo Bao-Fang Tang |
| 臺北醫學大學 |
2001 |
Hereditary gingival fibromatosis associated with periodontal disease: clinical diagnosis and treatment
|
呂炫?; Wu K-J; Lu H-K |
| 臺大學術典藏 |
2021-06-03T06:02:05Z |
Hereditary hearing impairment with cutaneous abnormalities
|
Lee T.-L.; Lin P.-H.; PEI-LUNG CHEN; Hong J.-B.; Wu C.-C. |
| 臺大學術典藏 |
2021-01-18T09:12:02Z |
Hereditary hearing impairment with cutaneous abnormalities
|
Lee, Tung Lin; PEI-HSUAN LIN; PEI-LUNG CHEN; JIN-BON HONG; CHEN-CHI WU |
| 臺大學術典藏 |
2021-07-06T02:03:48Z |
Hereditary hearing impairment with cutaneous abnormalities
|
Lee T.-L.; Lin P.-H.; PEI-LUNG CHEN; Hong J.-B.; Wu C.-C. |
| 臺大學術典藏 |
2021-09-07T03:54:09Z |
Hereditary Hearing Impairment with Cutaneous Abnormalities
|
Lee, Tung-Lin; Lin, Pei-Hsuan; Chen, Pei-Lung; Hong, Jin-Bon; Wu, Chen-Chi |
| 臺大學術典藏 |
2022-09-15T05:47:51Z |
Hereditary hearing impairment with cutaneous abnormalities
|
Lee T.-L.; Lin P.-H.; Chen P.-L.; Hong J.-B.; Chen-Chi Wu |
| 高雄醫學大學 |
2012 |
Hereditary hemorrhagic telangiectasia presenting as portal hypertension
|
趙家宏;莊世昌;陳榮祥;李金德 ; Chao, CH;Chuang, SC;Chen, JS;KT , Lee |
| 臺大學術典藏 |
2018-09-10T06:40:10Z |
Hereditary neuropathy with liability to pressure palsies: A clinical and electrophysiological study
|
Cheng, M.-L. and Jeng, J.-S. and Sung, S.-F. and Chang, Y.-C. and Huang, C.-C. and Chen R.-, C. and Hsieh, S.-T.; SUNG-TSANG HSIEH |
| 臺大學術典藏 |
2020-03-02T08:11:33Z |
Hereditary neuropathy with liability to pressure palsies: A clinical and electrophysiological study
|
Cheng M.-L.;Jeng J.-S.;Sung S.-F.;Chang Y.-C.;Huang C.-C.;Chen R.- C.;Sung-Tsang Hsieh; Cheng M.-L.; Jeng J.-S.; Sung S.-F.; Chang Y.-C.; Huang C.-C.; Chen R.- C.; SUNG-TSANG HSIEH |
| 臺大學術典藏 |
2020-03-03T03:46:14Z |
Hereditary neuropathy with liability to pressure palsies: A clinical and electrophysiological study
|
Cheng M.-L.; JIANN-SHING JENG; Sung S.-F.; Chang Y.-C.; Huang C.-C.; Chen R.- C.; Hsieh S.-T. |
| 臺大學術典藏 |
2020-11-03T11:45:23Z |
Hereditary neuropathy with liability to pressure palsies: A clinical and electrophysiological study
|
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. |
| 臺大學術典藏 |
2021-12-22T03:54:53Z |
Hereditary neuropathy with liability to pressure palsies: A clinical and electrophysiological study
|
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
|
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
|
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.
|
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
|
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 |
| 臺大學術典藏 |
2018-09-10T04:24:33Z |
Hereditary xanthinuria: report of two cases.
|
Chu, T.S.; TZONG-SHINN CHU |
| 臺大學術典藏 |
2021-07-20T03:15:56Z |
Hereditary xanthinuria: report of two cases.
|
TZONG-SHINN CHU |
