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"tsai l p"的相关文件
显示项目 1-10 / 37 (共4页)
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| 臺大學術典藏 |
2022-07-12T01:43:19Z |
High prevalence of lower urinary tract dysfunction in patients with Prader–Willi syndrome
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Chao T.-C.; Yang S.S.D.; SHANG-JEN CHANG; Tsai L.-P. |
| 臺大學術典藏 |
2022-07-12T01:43:07Z |
Elevated postvoid residual urine volume predicting recurrence of urinary tract infections in toilet-trained children
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SHANG-JEN CHANG; Tsai L.-P.; Hsu C.-K.; Yang S.S. |
| 臺大學術典藏 |
2021-01-27T06:53:36Z |
Firing activity of locus coeruleus noradrenergic neurons decreases in necdin-deficient mice, an animal model of Prader-Willi syndrome
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Wu, R.-N.;Hung, W.-C.;Chen, C.-T.;Tsai, L.-P.;Lai, W.-S.;Min, M.-Y.;Wong, S.-B.; Wu, R.-N.; Hung, W.-C.; Chen, C.-T.; Tsai, L.-P.; Lai, W.-S.; Min, M.-Y.; Wong, S.-B.; WEN-SUNG LAI |
| 臺大學術典藏 |
2021-01-27T03:23:37Z |
Firing activity of locus coeruleus noradrenergic neurons decreases in necdin-deficient mice, an animal model of Prader-Willi syndrome
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Wu, R.-N.;Hung, W.-C.;Chen, C.-T.;Tsai, L.-P.;Lai, W.-S.;Min, M.-Y.;Wong, S.-B.; Wu, R.-N.; Hung, W.-C.; Chen, C.-T.; Tsai, L.-P.; Lai, W.-S.; Min, M.-Y.; Wong, S.-B.; WEN-SUNG LAI |
| 臺大學術典藏 |
2021-01-04T07:38:59Z |
Corrigendum: Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type Ia (Human Molecular Genetics (1995) 4 (1095-1096))
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MEI-HWEI CHANG; Chang S.-M.; Wang T.-R.; Hwu W.-L.;Chuang S.-C.;Tsai L.-P.;Mei-Hwei Chang;Chang S.-M.;Wang T.-R.; Hwu W.-L.; Chuang S.-C.; Tsai L.-P. |
| 臺大學術典藏 |
2021-01-04T07:38:56Z |
Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type Ia
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Hwu W.-L.;Chuang S.-C.;Tsai L.-P.;Mei-Hwei Chang;Chuang S.-M.;Wang T.-R.; Hwu W.-L.; Chuang S.-C.; Tsai L.-P.; MEI-HWEI CHANG; Chuang S.-M.; Wang T.-R. |
| 臺大學術典藏 |
2021-01-04T07:38:56Z |
Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type la
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Hwu W.-L.;Chuang S.-C.;Tsai L.-P.;Mei-Hwei Chang;Chuang S.-M.;Wang T.-R.; Hwu W.-L.; Chuang S.-C.; Tsai L.-P.; MEI-HWEI CHANG; Chuang S.-M.; Wang T.-R. |
| 國立成功大學 |
2021 |
Epigenotype, genotype, and phenotype analysis of taiwanese patients with silver–russell syndrome
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Lin, H.-Y.;Lee, C.-L.;Fran, S.;Tu, R.-Y.;Chang, Y.-H.;Niu, D.-M.;Chang, Chang C.-Y.;Chiu, P.-C.;Chou, Y.-Y.;Hsiao, Hsiao H.-P.;Tsai, M.-C.;Chao, M.-C.;Tsai, L.-P.;Yang, C.-F.;Su, P.-H.;Pan, Y.-W.;Lee, C.-H.;Chu, T.-H.;Chuang, Chuang C.-K.;Lin, S.-P. |
| 臺大學術典藏 |
2020-12-29T08:15:37Z |
Firing activity of locus coeruleus noradrenergic neurons decreases in necdin-deficient mice, an animal model of Prader-Willi syndrome
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Wu, R.-N.;Hung, W.-C.;Chen, C.-T.;Tsai, L.-P.;Lai, W.-S.;Min, M.-Y.;Wong, S.-B.; Wu, R.-N.; Hung, W.-C.; Chen, C.-T.; Tsai, L.-P.; Lai, W.-S.; Min, M.-Y.; Wong, S.-B.; MING-YUAN MIN |
| 臺大學術典藏 |
2020-12-24T06:16:37Z |
Incidence of severe combined immunodeficiency through newborn screening in a Chinese population
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Yu H.-H.; Chang K.-L.; Chiang S.-C.; YIN-HSIU CHIEN; Lee W.-I.; Tsai L.-P.; Hsu L.-W.; Hu M.-H.; Hwu W.-L. |
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