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"wen yu tsai"
Showing items 46-68 of 68 (3 Page(s) Totally)
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| 臺大學術典藏 |
2018-09-10T04:05:38Z |
Familial nephrogenic diabetes insipidus: report of two families.
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Lee, J.S.;Tsai, W.Y.;Tsai, W.S.;Tsau, Y.K.;Chen, C.H.;Wang, T.R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T04:05:37Z |
Clinical characteristics and management of acute suppurative thyroiditis in children
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Chang, P.;Tsai, W.-Y.;Lee, P.-I.;Hsiao, P.-H.;Huang, L.-M.;Lee, J.-S.;Peng, S.-F.;Li, Y.-W.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T04:05:37Z |
Erratum: Clinical characteristics and management of acute suppurative thyroiditis in children (Journal of the Formosan Medical Association (2002) vol. 101 (468-71))
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Chang, P.;Tsai, W.Y.;Lee, P.I.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T04:05:37Z |
Neonatal screening for congenital adrenal hyperplasia in taiwan: A pilot study
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Chu, S.-Y.;Tsai, W.-Y.;Chen, L.-H.;Wei, M.-L.;Chien, Y.-H.;Hwu, W.-L.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T04:05:37Z |
Clinical experience of octreotide in the treatment of acromegaly
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Chang, T.-C.;Chang, C.-C.;Tsai, K.-S.;Huang, T.-S.;Tsai, W.-Y.;Lin, M.-H.;Chen, F.-W.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T04:05:37Z |
Congenital hypothyroidism in Taiwan: experience before mass screening.
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Tsai, W.Y.;Lee, J.S.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T03:51:36Z |
An epidemiological study of nocturnal enuresis in Taiwanese children
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Chang, P.;Chen, W.J.;Tsai, W.-Y.;Chiu, Y.-N.; WEI J. CHEN; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T03:41:51Z |
Intellectual outcome of patients with congenital hypothyroidism 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 |
2018-09-10T03:41:51Z |
Paraganglioma manifesting as shock: A case report
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Chang, P.;Tsai, W.-Y.;Lai, M.-K.;Wu, M.-H.;Tsau, Y.-K.;Peng, S.-F.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T03:41:51Z |
Prader-Willi syndrome with chromosome 15 interstitial deletion: report of one case.
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Hwu, W.L.;Tsai, W.Y.;Lee, J.S.;Wang, P.J.;Wang, T.R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T03:24:11Z |
Propylthiouracil-induced antineutrophil cytoplasm antibody-positive anaphylactoid purpura-like vasculitis - A case report
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Wang, L.-H.;Tsai, M.-J.;Tsai, W.-Y.;Lee, J.-S.;Chiang, B.-L.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T03:24:11Z |
Renal malformations in children with Turner's syndrome
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Chang, P.;Tsau, Y.-K.;Tsai, W.-Y.;Tsai, W.-S.;Hou, J.-W.;Hsiao, P.-H.;Lee, J.-S.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T03:24:11Z |
Islet cell and other organ-specific autoantibodies in Chinese children with insulin-dependent diabetes mellitus.
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WEN-YU TSAI; Tsai, W.Y.;Riley, W.J.;Lee, J.S.;Tsai, W.S. |
| 臺大學術典藏 |
2018-09-10T03:24:11Z |
Wiedemann-Beckwith syndrome with congenital central hypothyroidism in one of monozygotic twins.
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Chien, C.H.;Lee, J.S.;Tsai, W.Y.;Wang, T.R.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T03:24:10Z |
Genetic epidemiology of type 1 diabetes mellitus in Taiwan
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Chuang, L.-M.;Tsai, S.-T.;Juang, J.-H.;Tsai, W.-Y.;Tai, T.-Y.; LEE-MING CHUANG; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T03:24:10Z |
Late-onset holocarboxylase synthetase deficiency with homologous R508W mutation
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Hwu, W.-L.;Suzuki, Y.;Yang, X.;Li, X.;Chou, S.-P.;Narisawa, K.;Tsai, W.-Y.; WEN-YU TSAI |
| 臺大學術典藏 |
2018-09-10T03:24:10Z |
Autoimmune thyroiditis in children with Turner syndrome
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Chang, P.;Tsai, W.-Y.;Hou, J.-W.;Hsiao, P.-H.;Lee, J.-S.; WEN-YU TSAI |
| 中原大學 |
2012-07-17 |
創造性問題本位遊戲教學對六年級學生科技創造力的影響
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蔡文玉; Wen-Yu Tsai |
| 中原大學 |
2012-06-26 |
擁擠效果對大陸台商在不同產業群聚績效之影響
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蔡汶育; Wen-Yu Tsai |
| 臺大學術典藏 |
2007 |
Slipped capital femoral epiphysis as a complication of growth hormone therapy.
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WEN-YU TSAI; Wang, S.Y.;Tung, Y.C.;Tsai, W.Y.;Chien, Y.H.;Lee, J.S.;Hwu, W.L. |
| 臺大學術典藏 |
2003 |
Adrenoleukodystrophy initially diagnosed as idiopathic Addison's disease in two patients: The importance of early testing
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Hwu, W.-L.;Chien, Y.-H.;Liang, J.-S.;Lee, W.-T.;Wang, P.-J.;Tsai, W.-Y.; WEN-YU TSAI |
| 臺大學術典藏 |
1992 |
Hypothalamic hamartoma and precocious puberty: report of a case.
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Hsiao, P.H.;Tsai, W.Y.;Lee, J.S.;Liu, H.M.;Hsieh, F.J.; WEN-YU TSAI |
| 臺大學術典藏 |
1990 |
Restriction fragment length polymorphism study of families with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Taiwan.
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Lee, J.S.;Tsai, H.M.;Shieh, R.P.;Chen, S.H.;Tsai, W.Y.;Chung, B.C.; WEN-YU TSAI |
Showing items 46-68 of 68 (3 Page(s) Totally)
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