English  |  正體中文  |  简体中文  |  0  
???header.visitor??? :  53111499    ???header.onlineuser??? :  1046
???header.sponsordeclaration???
 
臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
???ui.leftmenu.abouttair???

???ui.leftmenu.bartitle???

???index.news???

???ui.leftmenu.copyrighttitle???

???ui.leftmenu.link???

"yanagawa y"???jsp.browse.items-by-author.description???

???jsp.browse.items-by-author.back???
???jsp.browse.items-by-author.order1??? ???jsp.browse.items-by-author.order2???

Showing items 1-6 of 6  (1 Page(s) Totally)
1 
View [10|25|50] records per page

Institution Date Title Author
臺大學術典藏 2020-11-04T01:59:21Z Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant dravet syndrome model during development Chang F.-C.; Hsiao J.H.; Khorkova O.; Liou H.-H.; Yanagawa Y.; Lee L.-J.; Lin S.-W.; Tsai M.-S.; Lee M.-L.; Chang C.-Y.; Fan H.-H.; Yu I.-S.; YOU-TZUNG CHEN; You J.-Y.; Chen C.-Y.
臺大學術典藏 2020-11-03T09:53:23Z Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant dravet syndrome model during development Tsai M.-S.;Lee M.-L.;Chang C.-Y.;Fan H.-H.;Yu I.-S.;Chen Y.-T.;You J.-Y.;Chen C.-Y.;Chang F.-C.;Hsiao J.H.;Khorkova O.;Horng-Huei Liou;Yanagawa Y.;Lee L.-J.;Lin S.-W.; Tsai M.-S.; Lee M.-L.; Chang C.-Y.; Fan H.-H.; Yu I.-S.; Chen Y.-T.; You J.-Y.; Chen C.-Y.; Chang F.-C.; Hsiao J.H.; Khorkova O.; HORNG-HUEI LIOU; Yanagawa Y.; Lee L.-J.; Lin S.-W.
臺大學術典藏 2020-03-02T05:45:40Z Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant dravet syndrome model during development Tsai M.-S.; Lee M.-L.; Chang C.-Y.; Fan H.-H.; Yu I.-S.; Chen Y.-T.; You J.-Y.; Chen C.-Y.; Chang F.-C.; Hsiao J.H.; Khorkova O.; Liou H.-H.; Yanagawa Y.; LI-JEN LEE; Lin S.-W.
臺大學術典藏 2020-02-26T07:30:11Z Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant dravet syndrome model during development Tsai M.-S; Lee M.-L; Chang C.-Y; Fan H.-H; Yu I.-S; Chen Y.-T; You J.-Y; Chen C.-Y; Chang F.-C; Hsiao J.H; Khorkova O; HORNG-HUEI LIOU; Yanagawa Y; Lee L.-J; Lin S.-W.
中國醫藥大學 2001 ATP7A gene mutations in 16 patients with Menkes disease and a patient with occipital horn syndrome Gu, YH; Kodama, H; Murata, Y; Mochizuki, D; Yanagawa, Y; Ushijima, H; Shiba, T; Lee, CC
中國醫藥大學 2001 ATP7A gene mutations in 16 patients with Menkes disease and a patient with occipital horn syndrome Gu, YH; Kodama, H; Murata, Y; Mochizuki, D; Yanagawa, Y; Ushijima, H; Shiba, T; Lee, CC

Showing items 1-6 of 6  (1 Page(s) Totally)
1 
View [10|25|50] records per page