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Institution	Date	Title	Author
臺大學術典藏	2022-04-08T09:23:06Z	Epstein-Barr virus BRLF1 induces genomic instability and progressive malignancy in nasopharyngeal carcinoma cells	Huang S.-Y.; Wu C.-C.; Cheng Y.-J.; Chou S.-P.; Jiang Y.-J.; Chu K.-C.; CHING-HWA TSAI; Lin S.-F.; Chen J.-Y.
臺大學術典藏	2022-04-08T09:23:05Z	Inhibition of Epstein-Barr virus reactivation by the flavonoid apigenin	Wu C.-C.; Fang C.-Y.; Cheng Y.-J.; Hsu H.-Y.; Chou S.-P.; Huang S.-Y.; CHING-HWA TSAI; Chen J.-Y.
臺大學術典藏	2021-06-29T08:16:06Z	Treatment and outcome of Taiwanese patients with 6-pyruvoyltetrahydropterin synthase gene mutations	Chien Y.-H.; Chiang S.-C.; Huang A.; Lin J.-M.; YEN-NAN CHIU; Chou S.-P.; Chu S.-Y.; Wang T.-R.; Hwu W.-L.
臺大學術典藏	2021-06-29T08:16:05Z	Phenylalanine hydroxylase deficiency: Intelligence of patients after early dietary treatment	Chien Y.-H.; Chiang S.-C.; Huang A.; Lin J.-M.; YEN-NAN CHIU; Chou S.-P.; Wang T.-R.; Hwu W.-L.
臺大學術典藏	2021-05-07T06:02:39Z	Familial tendency and risk of nasopharyngeal carcinoma in Taiwan: Effects of covariates on risk	Hsu W.-L.;Yu K.J.;Chien Y.-C.;Chun-Ju Chiang ;Cheng Y.-J.;Chen J.-Y.;Liu M.-Y.;Chou S.-P.;You S.-L.;Hsu M.-M.;Lou P.-J.;Wang C.-P.;Hong J.-H.;Leu Y.-S.;Tsai M.-H.;Su M.-C.;Tsai S.-T.;Chao W.-Y.;Ger L.-P.;Chen P.-R.;Yang C.-S.;Hildesheim A.;Diehl S.R.;Chen C.-J.; Hsu W.-L.; Yu K.J.; Chien Y.-C.; CHUN-JU CHIANG; Cheng Y.-J.; Chen J.-Y.; Liu M.-Y.; Chou S.-P.; You S.-L.; Hsu M.-M.; Lou P.-J.; Wang C.-P.; Hong J.-H.; Leu Y.-S.; Tsai M.-H.; Su M.-C.; Tsai S.-T.; Chao W.-Y.; Ger L.-P.; Chen P.-R.; Yang C.-S.; Hildesheim A.; Diehl S.R.; Chen C.-J.
臺大學術典藏	2020-12-24T06:17:24Z	Treatment and outcome of Taiwanese patients with 6-pyruvoyltetrahydropterin synthase gene mutations	YIN-HSIU CHIEN; Chiang S.-C.; Huang A.; Lin J.-M.; Chiu Y.-N.; Chou S.-P.; Chu S.-Y.; Wang T.-R.; Hwu W.-L.
臺大學術典藏	2020-12-24T06:17:20Z	Gene symbol: OTC: Disease: Ornithine carbamoyltransferase deficiency	Chiang S.-C.; Lin J.-M.; Chou S.-P.; Lul F.; Yeh H.-Y.; YIN-HSIU CHIEN; Huang Y.-T.; Hwu W.-L.
臺大學術典藏	2020-12-24T06:17:20Z	Gene Symbol: OTC: Disease: Ornithine carbamoyltransferase deficiency	Lin J.-M.; Chou S.-P.; Lul F.; Yeh H.-Y.; YIN-HSIU CHIEN; Huang Y.-T.; Hwu W.-L.; Chiang S.-C.
臺大學術典藏	2020-12-24T06:17:19Z	Mutation spectrum in Taiwanese patients with phenylalanine hydroxylase deficiency and a founder effect for the R241C mutation.	YIN-HSIU CHIEN; Chiang S.C.; Huang A.; Chou S.P.; Tseng S.S.; Huang Y.T.; Hwu W.L.
臺大學術典藏	2020-12-24T06:17:19Z	Poor outcome for neonatal-type nonketotic hyperglycinemia treated with high-dose sodium benzoate and dextromethorphan	YIN-HSIU CHIEN; Hsu C.-C.; Huang A.; Chou S.-P.; Lu F.-L.; Lee W.-T.; Hwu W.-L.
臺大學術典藏	2020-12-24T06:17:14Z	Phenylalanine hydroxylase deficiency: Intelligence of patients after early dietary treatment	YIN-HSIU CHIEN; Chiang S.-C.; Huang A.; Lin J.-M.; Chiu Y.-N.; Chou S.-P.; Wang T.-R.; Hwu W.-L.
臺大學術典藏	2020-12-24T06:16:24Z	Genotypic and phenotypic correlations of biotinidase deficiency in the Chinese population	Chang I.-F.; Hwu W.-L.; YIN-HSIU CHIEN; Hsu R.-H.; Ho H.-C.; Chou S.-P.; Huang T.-M.; Lee N.-C.
臺大學術典藏	2020-12-18T02:21:59Z	Poor outcome for neonatal-type nonketotic hyperglycinemia treated with high-dose sodium benzoate and dextromethorphan	Chien Y.-H.; Chien Y.-H.;Hsu C.-C.;Huang A.;Chou S.-P.;Lu F.-L.;Wang-Tso Lee;Hwu W.-L.; Hsu C.-C.; Huang A.; Chou S.-P.; Lu F.-L.; WANG-TSO LEE; Hwu W.-L.
臺大學術典藏	2020-12-16T02:26:31Z	Measurement of urinary orotic acid by gas chromatography-mass spectrometry.	WUH-LIANG HWU; Chou S.P.; Wang T.R.
臺大學術典藏	2020-12-16T02:26:30Z	Fragile-X mental retardation--a combination of cytogenetic and molecular approaches, with greater emphasis on DNA analysis.	Wang T.R.;Wuh-Liang Hwu;Hou J.W.;Chou S.P.;Liu C.H.; Wang T.R.; WUH-LIANG HWU; Hou J.W.; Chou S.P.; Liu C.H.
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	2020-12-16T02:26:21Z	A Chinese adult onset type II citrullinaemia patient with 851del4/1638ins23 mutations in the SLC25A13 gene.	Wuh-Liang Hwu;Kobayashi K.;Hu Y.H.;Yamaguchi N.;Saheki T.;Chou S.P.;Wang J.H.; WUH-LIANG HWU; Kobayashi K.; Hu Y.H.; Yamaguchi N.; Saheki T.; Chou S.P.; Wang J.H.
臺大學術典藏	2020-12-16T02:26:20Z	Treatment and outcome of Taiwanese patients with 6-pyruvoyltetrahydropterin synthase gene mutations	Chien Y.-H.;Chiang S.-C.;Huang A.;Lin J.-M.;Chiu Y.-N.;Chou S.-P.;Chu S.-Y.;Wang T.-R.;Wuh-Liang Hwu; Chien Y.-H.; Chiang S.-C.; Huang A.; Lin J.-M.; Chiu Y.-N.; Chou S.-P.; Chu S.-Y.; Wang T.-R.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:15Z	Gene Symbol: OTC: Disease: Ornithine carbamoyltransferase deficiency	Wuh-Liang Hwu;Huang Y.-T.;Chien Y.-H.;Yeh H.-Y.;Lul F.;Chou S.-P.;Lin J.-M.;Chiang S.-C.; WUH-LIANG HWU; Huang Y.-T.; Chien Y.-H.; Yeh H.-Y.; Lul F.; Chou S.-P.; Lin J.-M.; Chiang S.-C.
臺大學術典藏	2020-12-16T02:26:15Z	Gene symbol: OTC: Disease: Ornithine carbamoyltransferase deficiency	Wuh-Liang Hwu;Huang Y.-T.;Chien Y.-H.;Yeh H.-Y.;Lul F.;Chou S.-P.;Lin J.-M.;Chiang S.-C.; WUH-LIANG HWU; Huang Y.-T.; Chien Y.-H.; Yeh H.-Y.; Lul F.; Chou S.-P.; Lin J.-M.; Chiang S.-C.
臺大學術典藏	2020-12-16T02:26:14Z	Poor outcome for neonatal-type nonketotic hyperglycinemia treated with high-dose sodium benzoate and dextromethorphan	Chien Y.-H.;Hsu C.-C.;Huang A.;Chou S.-P.;Lu F.-L.;Lee W.-T.;Wuh-Liang Hwu; Chien Y.-H.; Hsu C.-C.; Huang A.; Chou S.-P.; Lu F.-L.; Lee W.-T.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:14Z	Mutation spectrum in Taiwanese patients with phenylalanine hydroxylase deficiency and a founder effect for the R241C mutation.	Chien Y.H.;Chiang S.C.;Huang A.;Chou S.P.;Tseng S.S.;Huang Y.T.;Wuh-Liang Hwu; Chien Y.H.; Chiang S.C.; Huang A.; Chou S.P.; Tseng S.S.; Huang Y.T.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:14Z	Phenotype and genotype analyses of ornithine transcarbamylase deficiency in Taiwanese	Huang Y.-T.;Chien Y.-H.;Yeh H.-Y.;Lin S.-J.;Lu F.L.;Chou S.-P.;Lin J.-M.;Chiang S.-H.;Wuh-Liang Hwu; Huang Y.-T.; Chien Y.-H.; Yeh H.-Y.; Lin S.-J.; Lu F.L.; Chou S.-P.; Lin J.-M.; Chiang S.-H.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:09Z	Phenylalanine hydroxylase deficiency: Intelligence of patients after early dietary treatment	Chien Y.-H.;Chiang S.-C.;Huang A.;Lin J.-M.;Chiu Y.-N.;Chou S.-P.;Wang T.-R.;Wuh-Liang Hwu; Chien Y.-H.; Chiang S.-C.; Huang A.; Lin J.-M.; Chiu Y.-N.; Chou S.-P.; Wang T.-R.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:25:32Z	Can a girl with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency live a normal life?	Tsai T.-Y.;Weng C.-Y.;Lin H.-M.;Lai P.-C.;Chou S.-P.;Wuh-Liang Hwu;Chu S.-Y.; Tsai T.-Y.; Weng C.-Y.; Lin H.-M.; Lai P.-C.; Chou S.-P.; WUH-LIANG HWU; Chu S.-Y.

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