臺大學術典藏 |
2020-12-16T02:26:24Z |
3-hydroxy-3-methylglutaric aciduria presenting with Reye like syndrome: Report of one case
|
Lee C.;Tsai F.-J.;Wu J.-Y.;Peng C.-T.;Tsai C.-H.;Wuh-Liang Hwu;Wang T.-R.;Millington D.S.; Lee C.; Tsai F.-J.; Wu J.-Y.; Peng C.-T.; Tsai C.-H.; WUH-LIANG HWU; Wang T.-R.; Millington D.S. |
國立臺灣大學 |
1991 |
A Clinical Observation in Achondroplasia
|
胡務亮; Wang, T. R.; Hwu, Wuh-Liang; Wang, T. R. |
臺大學術典藏 |
2020-12-16T02:26:32Z |
A clinical observation of achondroplasia.
|
Wuh-Liang Hwu;Wang T.R.; WUH-LIANG HWU; Wang T.R. |
國立成功大學 |
1998-06 |
A curvature-ovalization measurement apparatus for circular tubes under cyclic bending
|
Pan, Wen-Fung; Wang, T. R.; Hsu, C. M. |
臺大學術典藏 |
2020-12-16T02:26:33Z |
Alkaptonuria in a Chinese baby
|
Wang T.-R.; WUH-LIANG HWU |
國立臺灣大學 |
1989 |
Alkaptonuria in a Chinese Baby Case Report
|
Wang, T. R.; 胡務亮; Wang, T. R.; Hwu, Wuh-Liang |
臺大學術典藏 |
2020-12-16T02:26:25Z |
Allele distribution at the FMR1 locus in the general Chinese population
|
Chiang S.-C.;Lee Y.-M.;Wang T.-R.;Wuh-Liang Hwu; Chiang S.-C.; Lee Y.-M.; Wang T.-R.; WUH-LIANG HWU |
國立臺灣大學 |
1990 |
Apert Syndrome Associated with Septo-Optic Dysplasia
|
沈友仁; 滕儒錚; 王本榮; Wang, T. R.; Shen, Y. Z.; 沈友仁; 滕儒錚; Wang, Pen-Jung; Wang, T. R.; Shen, Y. Z. |
臺大學術典藏 |
2020-12-16T02:26:27Z |
Arylsulfatase A pseudodeficiency in Chinese
|
Wuh-Liang Hwu;Tsai L.-P.;Wang W.-C.;Chuang S.-C.;Wang P.-J.;Wang T.-R.; WUH-LIANG HWU; Tsai L.-P.; Wang W.-C.; Chuang S.-C.; Wang P.-J.; Wang T.-R. |
國立臺灣大學 |
1993 |
Atlantoaxial Subluxation and Syringomyelia in Down Syndrome
|
王本榮; Hou, J. W.; Lin, Y. J.; Wang, T. R.; Wang, Pen-Jung; Hou, J. W.; Lin, Y. J.; Wang, T. R. |
臺大學術典藏 |
2020-06-29T01:39:39Z |
Author Correction: Hyperpolarization of the subthalamic nucleus alleviates hyperkinetic movement disorders (Scientific Reports, (2020), 10, 1, (8278), 10.1038/s41598-020-65211-w)
|
Tai C.-H.;Ming-Kai Pan;Tseng S.-H.;Wang T.-R.;Kuo C.-C.; Tai C.-H.; MING-KAI PAN; Tseng S.-H.; Wang T.-R.; Kuo C.-C. |
臺大學術典藏 |
2020-06-30T07:15:18Z |
Author Correction: Hyperpolarization of the subthalamic nucleus alleviates hyperkinetic movement disorders (Scientific Reports, (2020), 10, 1, (8278), 10.1038/s41598-020-65211-w)
|
Tai C.-H.;Pan M.-K.;Tseng S.-H.;Wang T.-R.;Chung-Chin Kuo; Tai C.-H.; Pan M.-K.; Tseng S.-H.; Wang T.-R.; Chung-Chin Kuo |
臺大學術典藏 |
2020-11-03T12:21:46Z |
Author Correction: Hyperpolarization of the subthalamic nucleus alleviates hyperkinetic movement disorders (Scientific Reports, (2020), 10, 1, (8278), 10.1038/s41598-020-65211-w)
|
Chun-Hwei Tai;Pan M.-K.;Tseng S.-H.;Wang T.-R.;Kuo C.-C.; CHUN-HWEI TAI; Pan M.-K.; Tseng S.-H.; Wang T.-R.; Kuo C.-C. |
臺大學術典藏 |
2021-05-18T05:54:27Z |
Author Correction: Hyperpolarization of the subthalamic nucleus alleviates hyperkinetic movement disorders (Scientific Reports, (2020), 10, 1, (8278), 10.1038/s41598-020-65211-w)
|
Tai C.-H.; Pan M.-K.; SHENG-HONG TSENG; Wang T.-R.; Kuo C.-C. |
臺大學術典藏 |
2021-07-08T03:25:54Z |
Bony changes in common mucopolysaccharidoses
|
SHYH-JYE CHEN; Li, Y W; Wang, T R; Hsu, J C |
臺大學術典藏 |
2022-03-09T06:48:39Z |
Camptomelic dysplasia: report of one case
|
Tsao, P. N.; Teng, R. J.; WUH-LIANG HWU; Tsou Yau, K. I.; Wang, T. R. |
臺大學術典藏 |
2018-09-10T05:46:28Z |
Camptomelic dysplasia: report of one case.
|
Tsao, P.N.;Teng, R.J.;Hwu, W.L.;Tsou Yau, K.I.;Wang, T.R.; PO-NIEN TSAO |
臺大學術典藏 |
2020-12-16T02:26:31Z |
Cardiovascular disorders in Turner's syndrome and its correlation to karyotype.
|
Hou J.W.; WUH-LIANG HWU; Tsai W.Y.; Lee J.S.; Wang T.R.; Lue H.C. |
臺大學術典藏 |
2020-12-16T02:26:23Z |
Carnitine transport defect presenting with hyperammonemia: Report of one case
|
Wuh-Liang Hwu;Chiang S.-C.;Chang M.-H.;Wang T.-R.; WUH-LIANG HWU; Chiang S.-C.; Chang M.-H.; Wang T.-R. |
臺大學術典藏 |
2021-01-04T07:38:42Z |
Carnitine transport defect presenting with hyperammonemia: Report of one case
|
Hwu W.-L.;Chiang S.-C.;Mei-Hwei Chang;Wang T.-R.; Hwu W.-L.; Chiang S.-C.; MEI-HWEI CHANG; Wang T.-R. |
國立臺灣大學 |
1994 |
Case Report:Fucosidosis in a Chinese Girl
|
胡務亮; Chuang, S. C.; Wang, W. C.; Wang, T. R.; Hwu, Wuh-Liang; Chuang, S. C.; Wang, W. C.; Wang, T. R. |
臺大學術典藏 |
2018-09-10T06:14:53Z |
CATCH 22: Deletion of locus 22Q11 in velocardiofacial syndrome, digeorge anomaly, and nonsyndromic conotruncal defects
|
Hou, J.-W.;Wang, J.-K.;Tsai, W.-Y.;Chou, C.-C.;Wang, T.-R.; WEN-YU TSAI |
臺大學術典藏 |
2021-01-06T05:51:00Z |
CATCH 22: Deletion of locus 22Q11 in velocardiofacial syndrome, digeorge anomaly, and nonsyndromic conotruncal defects
|
Hou J.-W.; JOU-KOU WANG; Tsai W.-Y.; Chou C.-C.; Wang T.-R. |
臺大學術典藏 |
2021-03-10T08:56:26Z |
Common variable immunodeficiency: An immunological study
|
Keh-Sung Tsai;Chuang C.Y.;Hsieh K.H.;Wang T.R.;Luh K.T.;Hsu H.C.; KEH-SUNG TSAI; Chuang C.Y.; Hsieh K.H.; Wang T.R.; Luh K.T.; Hsu H.C. |
臺大學術典藏 |
2021-05-26T03:36:28Z |
Common variable immunodeficiency: An immunological study
|
Tsai K.S.; Chuang C.Y.; Hsieh K.H.; Wang T.R.; KWEN-TAY LUH; Hsu H.C. |