臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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Showing items 121-130 of 288 (29 Page(s) Totally)
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Institution	Date	Title	Author
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	2020-12-16T02:26:02Z	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	2020-12-16T02:25:43Z	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	2020-12-09T01:38:33Z	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.

Showing items 121-130 of 288 (29 Page(s) Totally)
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