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"wen yu tsai"
Showing items 6-30 of 68 (3 Page(s) Totally)
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| 臺大學術典藏 |
2021-06-07T07:59:31Z |
Symptomatic Hypomagnesemia in Children
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Yong-Kwei Tsau; Wen-Yu Tsai; FRANK LEIGH LU; Wen-Shiung Tsai; Chiung-Hui Chen |
| 臺大學術典藏 |
2019-10-19T01:46:51Z |
Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith-Wiedemann spectrum
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NI-CHUNG LEE; NI-CHUNG LEE;WEN-YU TSAI;SHIH-YAO LIU;Jong, Yiin-Jeng;Su, Yi-Ning;Chen, Ming;HUEY-LING CHEN;YUNG-LI YANG;KUAN-TING KUO;MU-ZON WU;WEN-HSI LIN;JIN-CHUNG SHIH;WUH-LIANG HWU;YI-CHING TUNG;CHENG-TING LEE; CHENG-TING LEE; YI-CHING TUNG; WUH-LIANG ??HWU; JIN-CHUNG SHIH; WEN-HSI LIN; MU-ZON WU; KUAN-TING KUO; YUNG-LI YANG; HUEY-LING CHEN; Chen, Ming; Su, Yi-Ning; Jong, Yiin-Jeng; SHIH-YAO LIU; WEN-YU TSAI |
| 臺大學術典藏 |
2019-09-24T01:37:46Z |
The spectrum of 45,X/46,XY mosaicism in Taiwanese children: The experience of a single center
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WEN-YU TSAI;HONG-NERNG HO;YI-CHING TUNG;SHIH-YAO LIU;MU-ZON WU;CHENG-TING LEE;Huang, Yen-Chun; Huang, Yen-Chun; CHENG-TING LEE; MU-ZON WU; SHIH-YAO LIU; YI-CHING TUNG; HONG-NERNG HO; WEN-YU TSAI |
| 臺大學術典藏 |
2019-01-05T07:20:19Z |
Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome
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Kuo, Pei-Wen;Tu, Mei-Pin;Fang, Mei-Ya;Chen, Lang-Yao;Niu, Dau-Ming;Li, Ni-Chung;Lin, Shuan-Pei;Su, Yi-Ning;Hung, Chia-Cheng;Lin, Chiou-Ya;HONG-NERNG HO;WEN-MING HSU;YI-CHING TUNG;WU-SHIUN HSIEH;WEN-YU TSAI;CHIEN-NAN LEE;SHIN-YU LIN; SHIN-YU LIN; CHIEN-NAN LEE; Hung, Chia-Cheng; WEN-YU TSAI; Lin, Shuan-Pei; Li, Ni-Chung; WU-SHIUN HSIEH; YI-CHING TUNG; Niu, Dau-Ming; WEN-MING HSU; Chen, Lang-Yao; Fang, Mei-Ya; Tu, Mei-Pin; Kuo, Pei-Wen; Lin, Chiou-Ya; Su, Yi-Ning; HONG-NERNG HO |
| 臺大學術典藏 |
2018-09-10T14:50:28Z |
Cyclic pamidronate infusion for neonatal-onset Osteogenesis imperfecta
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Lin, Chia-Hsuan;Chien, Yin-Hsiu;Peng, Shinn-Forng;Tsai, Wen-Yu;Tung, Yi-Ching;Lee, Cheng-Ting;Chien, Chun-Ching;Hwu, Wuh-Liang;Lee, Ni-Chung; Lin, C.-H. and Chien, Y.-H. and Peng, S.-F. and Tsai, W.-Y. and Tung, Y.-C. and Lee, C.-T. and Chien, C.-C. and Hwu, W.-L. and Lee, N.-C.; 蔡文友;胡務亮;童怡靖;彭信逢;李正婷;李妮鍾;簡穎秀; NI-CHUNG LEE; Lin, Chia-Hsuan; YI-CHING TUNG; Chien, Yin-Hsiu; CHENG-TING LEE; Peng, Shinn-Forng; YIN-HSIU CHIEN; Tsai, Wen-Yu; Tung, Yi-Ching; WUH-LIANG HWU; Lee, Cheng-Ting; WEN-YU TSAI; Chien, Chun-Ching; Hwu, Wuh-Liang; Lee, Ni-Chung; �^�H�{ |
| 臺大學術典藏 |
2018-09-10T09:40:39Z |
Clinical characteristics of central diabetes insipidus in taiwanese children
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Liu, Shih-Yao;Tung, Yi-Ching;Lee, Cheng-Ting;Liu, Hon-Man;Peng, Shinn-Forng;Wu, Mu-Zon;Kuo, Meng-Fai;Tsai, Wen-Yu; Liu, S.-Y. and Tung, Y.-C. and Lee, C.-T. and Liu, H.-M. and Peng, S.-F. and Wu, M.-Z. and Kuo, M.-F. and Tsai, W.-Y.; 蔡文友 ;吳木榮 ;童怡靖 ;彭信逢 ;廖漢文 ;郭夢菲; MENG-FAI KUO; Liu, Shih-Yao; YI-CHING TUNG; Tung, Yi-Ching; Lee, Cheng-Ting; SHIH-YAO LIU; CHENG-TING LEE; Liu, Hon-Man; MU-ZON WU; Peng, Shinn-Forng; HON-MAN LIU; Wu, Mu-Zon; WEN-YU TSAI; Tsai, Wen-Yu; ?^?H?{ |
| 臺大學術典藏 |
2018-09-10T08:22:30Z |
Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome
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Lin, S.-Y. and Lee, C.-N. and Hung, C.-C. and Tsai, W.-Y. and Lin, S.-P. and Li, N.-C. and Hsieh, W.-S. and Tung, Y.-C. and Niu, D.-M. and Hsu, W.-M. and Chen, L.-Y. and Fang, M.-Y. and Tu, M.-P. and Kuo, P.-W. and Lin, C.-Y. and Su, Y.-N. and Ho, H.-N.; WU-SHIUN HSIEH; SHIN-YU LIN; WEN-MING HSU; HONG-NERNG HO; YI-CHING TUNG; CHIEN-NAN LEE; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T08:04:53Z |
Cushings disease in children: Report of three cases
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Hsu, P.-Y. and Tung, Y.-C. and Lee, C.-T. and Lo, F.-S. and Wu, M.-Z. and Tsai, W.-Y. and Tu, Y.-K.; YI-CHING TUNG; CHENG-TING LEE; MU-ZON WU; Yong-Kwang Tu; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T08:04:43Z |
Premature thelarche in Taiwanese girls
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Lee, C.-T.;Tung, Y.-C.;Tsai, W.-Y.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T07:22:21Z |
Secondary hypertension in children
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Lin, J.-H.;Tsau, Y.-K.;Tsai, W.-Y.;Wu, M.-H.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T07:22:20Z |
Detection of KAL-1 gene deletion with fluorescence in situ hybridization
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Hou, J.-W.;Tsai, W.-Y.;Wang, T.-R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T07:22:20Z |
Intellectual outcomes of patients with congenital hypothyroidism not detected by neonatal screening
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Hsiao, P.-H.;Chiu, Y.-N.;Tsai, W.-Y.;Su, S.-C.;Lee, J.-S.;Soong, W.-T.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T07:22:20Z |
Longitudinal study of serum free thyroxine and thyrotropin levels by chemiluminescent immunoassay during infancy
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Lu, F.L.;Tsou Yau, K.-I.;Tsai, K.-S.;Tang, J.-R.;Tsao, P.-N.;Tsai, W.-Y.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T07:22:20Z |
Nephrocalcinosis in childhood
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Lin, M.-T.;Tsau, Y.-K.;Tsai, W.-Y.;Tsai, W.-S.;Lu, F.L.;Hsiao, P.-H.;Chen C.-, H.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T06:41:38Z |
Anti-GAD65 autoantibody in Taiwanese patients with insulin-dependent diabetes mellitus: Effect of HLA on anti-GAD65 positivity and clinical characteristics
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Chuang, L.-M.;Lin, C.-Y.;Wu, H.-P.;Tsai, W.-Y.;Tai, T.-Y.;Lin, B.J.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T06:14:53Z |
Anti-GAD65 autoantibody in Taiwanese patients with insulin-dependent diabetes mellitus: Effect of HLA on anti-GAD65 positivity and clinical characteristics
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Chuang, L.-M.;Lin, C.-Y.;Wu, H.-P.;Tsai, W.-Y.;Tai, T.-Y.;Lin, B.J.; WEN-YU TSAI |
| 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
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Hou, J.-W.;Wang, J.-K.;Tsai, W.-Y.;Chou, C.-C.;Wang, T.-R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T06:14:53Z |
Clinical significance of thyrotropin-binding inhibitor immunoglobulin levels in newborns and their mothers
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Huang, C.-Y.;Chang, T.-C.;Tsai, W.-Y.;Hsiao, Y.-L.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T06:14:53Z |
Partial DiGeorge anomaly associated with 10p deletion
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Hsu, H.-L.;Hsiao, P.-H.;Hou, J.-W.;Tsai, W.-Y.;Wang, T.-R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T05:46:39Z |
HLA DRB1/DQA1/DQB1 haplotype determines thyroid autoimmunity in patients with insulin-dependent diabetes mellitus
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Chuang, L.-M.;Wu, H.-P.;Chang, C.-C.;Tsai, W.-Y.;Chang, H.-M.;Tai, T.-Y.;Lin, B.J.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T05:46:39Z |
Kleine-Levin syndrome in a boy with Prader-Willi syndrome
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Gau, S.-F.;Soong, W.-T.;Liu, H.-M.;Hou, J.-W.;Tsai, W.-Y.;Chiu, Y.-N.;Yeh, Y.-C.;Wang, P.-J.;Wang, T.-R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T05:46:39Z |
Mitochondrial gene mutations in patients with insulin-dependent diabetes mellitus in Taiwan
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Chuang, L.-M.;Wu, H.-P.;Tsai, W.-Y.;Lai, C.-S.;Tai, T.-Y.;Lin, B.J.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T05:46:39Z |
Urinary N-acetyl-beta-D-glucosaminidase activity in children with insulin-dependent diabetes mellitus
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Hsiao, P.-H.;Tsai, W.-S.;Tsai, W.-Y.;Lee, J.-S.;Tsau, Y.-K.;Chen, C.-H.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T05:12:25Z |
Dynamic enhancement MRI of anterior lobe in pituitary dwarfism
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Liu, H.M.;Li, Y.W.;Tsai, W.Y.;Su, C.T.; HON-MAN LIU; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T05:12:25Z |
Novel deletion mutations of the DAX1 (NR0B1) gene in two Taiwanese families with X-linked adrenal hypoplasia congenita
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Tsai, W.-Y.;Tung, Y.-C.; WEN-YU TSAI |
Showing items 6-30 of 68 (3 Page(s) Totally)
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View [10|25|50] records per page
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