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機構 日期 題名 作者
臺大學術典藏 2020-12-18T02:21:59Z Adrenoleukodystrophy initially diagnosed as idiopathic Addison's disease in two patients: The importance of early testing Tsai W.-Y.; Wang P.-J.; WANG-TSO LEE; Liang J.-S.; Chien Y.-H.; Hwu W.-L.; Hwu W.-L.;Chien Y.-H.;Liang J.-S.;Wang-Tso Lee;Wang P.-J.;Tsai W.-Y.
臺大學術典藏 2020-12-16T07:22:06Z Hypogonadotropic Hypogonadism and Hematologic Phenotype in Patients with Transfusion-Dependent Beta-Thalassemia Chern J.P.S.;Lin K.-H.;Tsai W.-Y.;Wang S.-C.;Meng-Yao Lu;Lin D.-T.;Lin K.-S.;Lo S.H.; Chern J.P.S.; Lin K.-H.; Tsai W.-Y.; Wang S.-C.; MENG-YAO LU; Lin D.-T.; Lin K.-S.; Lo S.H.
臺大學術典藏 2020-12-16T07:21:54Z Endocrine dysfunction in Taiwanese children with human chorionic gonadotropin-secreting germ cell tumors Lin C.-M.; Lee C.-T.; Tung Y.-C.; Wu M.-Z.; Tsai W.-Y.; Yang Y.-L.; MENG-YAO LU; Jou S.-T.; Lin D.-T.; Lin K.-H.
臺大學術典藏 2020-12-16T02:26:32Z Prader-Willi syndrome with chromosome 15 interstitial deletion: report of one case. Wuh-Liang Hwu;Tsai W.Y.;Lee J.S.;Wang P.J.;Wang T.R.; WUH-LIANG HWU; Tsai W.Y.; Lee J.S.; Wang P.J.; Wang T.R.
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 Late-onset holocarboxylase synthetase deficiency with homologous R508W mutation Wuh-Liang Hwu;Suzuki Y.;Yang X.;Li X.;Chou S.-P.;Narisawa K.;Tsai W.-Y.; WUH-LIANG HWU; Suzuki Y.; Yang X.; Li X.; Chou S.-P.; Narisawa K.; Tsai W.-Y.
臺大學術典藏 2020-12-16T02:26:18Z Neonatal screening for congenital adrenal hyperplasia in taiwan: A pilot study Chu S.-Y.;Tsai W.-Y.;Chen L.-H.;Wei M.-L.;Chien Y.-H.;Wuh-Liang Hwu; Chu S.-Y.; Tsai W.-Y.; Chen L.-H.; Wei M.-L.; Chien Y.-H.; WUH-LIANG HWU
臺大學術典藏 2020-12-16T02:26:17Z Neonatal screening and monitoring system in Taiwan. Wuh-Liang Hwu;Huang A.C.;Chen J.S.;Hsiao K.J.;Tsai W.Y.; WUH-LIANG HWU; Huang A.C.; Chen J.S.; Hsiao K.J.; Tsai W.Y.
臺大學術典藏 2020-12-16T02:26:16Z Adrenoleukodystrophy initially diagnosed as idiopathic Addison's disease in two patients: The importance of early testing Wuh-Liang Hwu;Chien Y.-H.;Liang J.-S.;Lee W.-T.;Wang P.-J.;Tsai W.-Y.; WUH-LIANG HWU; Chien Y.-H.; Liang J.-S.; Lee W.-T.; Wang P.-J.; Tsai W.-Y.
臺大學術典藏 2020-12-16T02:26:11Z Terminal deletion of chromosome 2q associated with Graves' disease: A case report and literature review Chu S.-Y.;Tsai W.-Y.;Chien Y.-H.;Fang J.-S.;Ku C.-W.;Chang P.-Y.;Wuh-Liang Hwu; Chu S.-Y.; Tsai W.-Y.; Chien Y.-H.; Fang J.-S.; Ku C.-W.; Chang P.-Y.; WUH-LIANG HWU
臺大學術典藏 2020-12-16T02:26:02Z Slipped capital femoral epiphysis as a complication of growth hormone therapy. Wang S.Y.;Tung Y.C.;Tsai W.Y.;Chien Y.H.;Lee J.S.;Wuh-Liang Hwu; Wang S.Y.; Tung Y.C.; Tsai W.Y.; Chien Y.H.; Lee J.S.; WUH-LIANG HWU
臺大學術典藏 2020-12-16T02:25:52Z Caloric restriction in Alstr?m syndrome prevents hyperinsulinemia Lee N.-C.;Marshall J.D.;Collin G.B.;Naggert J.K.;Chien Y.-H.;Tsai W.-Y.;Wuh-Liang Hwu; Lee N.-C.; Marshall J.D.; Collin G.B.; Naggert J.K.; Chien Y.-H.; Tsai W.-Y.; WUH-LIANG HWU
臺大學術典藏 2020-12-16T02:25:43Z Congenital hypopituitarism due to POU1F1 gene mutation Lee N.-C.;Tsai W.-Y.;Peng S.-F.;Tung Y.-C.;Chien Y.-H.;Wuh-Liang Hwu; Lee N.-C.; Tsai W.-Y.; Peng S.-F.; Tung Y.-C.; Chien Y.-H.; WUH-LIANG HWU
臺大學術典藏 2020-12-16T02:25:27Z Cyclic pamidronate infusion for neonatal-onset Osteogenesis imperfecta Lin C.-H.; Chien Y.-H.; Peng S.-F.; Tsai W.-Y.; Tung Y.-C.; Lee C.-T.; Chien C.-C.; WUH-LIANG HWU; Lee N.-C.
臺大學術典藏 2020-12-16T02:25:15Z Clinical characteristics of Taiwanese children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency detected by neonatal screening Liu S.-Y.;Lee C.-T.;Tung Y.-C.;Chien Y.-H.;Wuh-Liang Hwu;Tsai W.-Y.; Liu S.-Y.; Lee C.-T.; Tung Y.-C.; Chien Y.-H.; WUH-LIANG HWU; Tsai W.-Y.
臺大學術典藏 2020-12-16T02:25:14Z Comprehensive human leukocyte antigen genotyping of patients with type 1 diabetes mellitus in Taiwan Tung Y.-C.;Fann C.S.-J.;Chang C.-C.;Chu C.-C.;Yang W.-S.;Wuh-Liang Hwu;Chen P.-L.;Tsai W.-Y.; Tung Y.-C.; Fann C.S.-J.; Chang C.-C.; Chu C.-C.; Yang W.-S.; WUH-LIANG HWU; Chen P.-L.; Tsai W.-Y.
臺大學術典藏 2020-12-16T02:25:12Z SHOX deficiency in short Taiwanese children: A single-center experience Tung Y.-C.;Lee N.-C.;Wuh-Liang Hwu;Liu S.-Y.;Lee C.-T.;Chien Y.-H.;Tsai W.-Y.; Tung Y.-C.; Lee N.-C.; WUH-LIANG HWU; Liu S.-Y.; Lee C.-T.; Chien Y.-H.; Tsai W.-Y.
臺大學術典藏 2020-12-16T02:25:10Z Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum Lee C.-T.;Tung Y.-C.;Wuh-Liang Hwu;Shih J.-C.;Lin W.-H.;Wu M.-Z.;Kuo K.-T.;Yang Y.-L.;Chen H.-L.;Chen M.;Su Y.-N.;Jong Y.-J.;Liu S.-Y.;Tsai W.-Y.;Lee N.-C.; Lee C.-T.; Tung Y.-C.; WUH-LIANG HWU; Shih J.-C.; Lin W.-H.; Wu M.-Z.; Kuo K.-T.; Yang Y.-L.; Chen H.-L.; Chen M.; Su Y.-N.; Jong Y.-J.; Liu S.-Y.; Tsai W.-Y.; Lee N.-C.
臺大學術典藏 2020-12-16T02:25:02Z Thyroid disorders in Taiwanese children with Down syndrome: The experience of a single medical center Liu M.-Y.;Lee C.-T.;Lee N.-C.;Tung Y.-C.;Chien Y.-H.;Wuh-Liang Hwu;Tsai W.-Y.; Liu M.-Y.; Lee C.-T.; Lee N.-C.; Tung Y.-C.; Chien Y.-H.; WUH-LIANG HWU; Tsai W.-Y.
臺大學術典藏 2020-12-15T07:42:46Z Persistent hyperinsulinemic hypoglycemia due to nesidiodysplasia in a neonate LUAN-YIN CHANG; Tsai W.-Y.; Huang S.-F.; Yau K.-I.T.; Li Y.-W.; Chen C.-C.
臺大學術典藏 2020-12-09T05:58:47Z Nephrocalcinosis in childhood Chen C.-H.;Lin M.-T.;Tsau Y.-K.;Tsai W.-Y.;Tsai W.-S.;Frank Leigh Lu;Hsiao P.-H.; Chen C.-H.; Lin M.-T.; Tsau Y.-K.; Tsai W.-Y.; Tsai W.-S.; FRANK LEIGH LU; Hsiao P.-H.
臺大學術典藏 2020-12-09T01:38:38Z Caloric restriction in Alstr?m syndrome prevents hyperinsulinemia NI-CHUNG LEE; Marshall J.D.; Collin G.B.; Naggert J.K.; Chien Y.-H.; Tsai W.-Y.; Hwu W.-L.
臺大學術典藏 2020-12-09T01:38:33Z Congenital hypopituitarism due to POU1F1 gene mutation Ni-Chung Lee;Tsai W.-Y.;Peng S.-F.;Tung Y.-C.;Chien Y.-H.;Hwu W.-L.; NI-CHUNG LEE; Tsai W.-Y.; Peng S.-F.; Tung Y.-C.; Chien Y.-H.; Hwu W.-L.
臺大學術典藏 2020-12-09T01:38:18Z Russell–Silver syndrome presenting with ambiguous genitalia Chang I.-F.;Chien Y.-H.;Tsai W.-Y.;Ni-Chung Lee; Chang I.-F.; Chien Y.-H.; Tsai W.-Y.; NI-CHUNG LEE
臺大學術典藏 2020-12-09T01:38:15Z SHOX deficiency in short Taiwanese children: A single-center experience Tung Y.-C.;Ni-Chung Lee;Hwu W.-L.;Liu S.-Y.;Lee C.-T.;Chien Y.-H.;Tsai W.-Y.; Tung Y.-C.; NI-CHUNG LEE; Hwu W.-L.; Liu S.-Y.; Lee C.-T.; Chien Y.-H.; Tsai W.-Y.

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