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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
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Repositories
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2019臺灣學術機構典藏
研討會
機構典藏系統RC7版本已
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Institution Date Title Author
臺大學術典藏 2020-12-21T01:58:21Z ADHD-related symptoms, emotional/behavioral problems, and physical conditions in Taiwanese children with epilepsy Chiu Y.-N.; Gau S.S.F.; Lin W.-S.; PI-CHUAN FAN; Lee W.-T.; Lee C.-M.; Liu S.-T.; Tsai F.-J.; Tsai F.-J.;Liu S.-T.;Lee C.-M.;Lee W.-T.;Pi-Chuan Fan;Lin W.-S.;Chiu Y.-N.;Gau S.S.F.
臺大學術典藏 2020-12-21T01:58:21Z Molecular aspects of Dravet syndrome patients in Taiwan Tsai F.-J.; Tsai C.-H.; Chou I.-C.; Tsai Y.; Lin W.-C.; Weng W.-C.; PI-CHUAN FAN; Chen S.-J.; Lin W.-D.;Chang K.-P.;Wang C.-H.;Chen S.-J.;Pi-Chuan Fan;Weng W.-C.;Lin W.-C.;Tsai Y.;Tsai C.-H.;Chou I.-C.;Tsai F.-J.; Lin W.-D.; Chang K.-P.; Wang C.-H.
臺大學術典藏 2020-12-18T02:21:47Z Sleep problems in children with autism, attention-deficit hyperactivity disorder, and epilepsy Chiu Y.-N.; Wu Y.-Y.; Tsai F.-J.; Chiang H.-L.; Lee C.-M.; Gau S.S.-F.; WANG-TSO LEE; Fan P.-C.
臺大學術典藏 2020-12-16T02:26:32Z Niemann-Pick disease type B with ocular involvement: report of a case. Tsai F.J.;Peng C.T.;Tsai C.H.;Wuh-Liang Hwu;Wang T.R.; Tsai F.J.; Peng C.T.; Tsai C.H.; WUH-LIANG HWU; Wang T.R.
臺大學術典藏 2020-12-16T02:26:29Z Molecular diagnosis of Gaucher disease type II. Tsai F.J.;Chen H.W.;Peng C.T.;Tsai C.H.;Wuh-Liang Hwu;Wang T.R.;Liu S.C.; Tsai F.J.; Chen H.W.; Peng C.T.; Tsai C.H.; WUH-LIANG HWU; Wang T.R.; Liu S.C.
臺大學術典藏 2020-12-16T02:26:28Z Sex determination in infants with ambiguous genitalia using the polymerase chain reaction of SRY gene. Tsai F.J.;Tsai C.H.;Wuh-Liang Hwu;Wang T.R.;Shu S.G.;Liu S.C.; Tsai F.J.; Tsai C.H.; WUH-LIANG HWU; Wang T.R.; Shu S.G.; Liu S.C.
臺大學術典藏 2020-12-16T02:26:25Z Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with apert syndrome Tsai F.-J.; WUH-LIANG HWU; Lin S.-P.; Chang J.-G.; Wang T.-R.; Tsai C.-H.
臺大學術典藏 2020-12-16T02:26:24Z 3-hydroxy-3-methylglutaric aciduria presenting with Reye like syndrome: Report of one case Lee C.;Tsai F.-J.;Wu J.-Y.;Peng C.-T.;Tsai C.-H.;Wuh-Liang Hwu;Wang T.-R.;Millington D.S.; Lee C.; Tsai F.-J.; Wu J.-Y.; Peng C.-T.; Tsai C.-H.; WUH-LIANG HWU; Wang T.-R.; Millington D.S.
臺大學術典藏 2020-12-16T02:26:12Z Detection of a homozygous D645E mutation of the acid α-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II [3] Chen C.-P.;Lin S.-P.;Tzen C.-Y.;Tsai F.-J.;Wuh-Liang Hwu;Wang W.; Chen C.-P.; Lin S.-P.; Tzen C.-Y.; Tsai F.-J.; WUH-LIANG HWU; Wang W.
臺大學術典藏 2020-12-16T02:26:04Z Mutation analysis of Gaucher disease patients in Taiwan: High prevalence of the RecNciI and L444P mutations Wan L.;Hsu C.-M.;Tsai C.-H.;Lee C.-C.;Wuh-Liang Hwu;Tsai F.-J.; Wan L.; Hsu C.-M.; Tsai C.-H.; Lee C.-C.; WUH-LIANG HWU; Tsai F.-J.

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