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Showing items 596-605 of 770  (77 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2020-03-03T03:06:22Z Gene therapy improves brain white matter in aromatic l-amino acid decarboxylase deficiency Tseng C.-H.; Chien Y.-H.; Lee N.-C.; Hsu Y.-C.; Peng S.-F.; WEN-YIH TSENG; Hwu W.-L.
臺大學術典藏 2020-03-03T02:33:35Z Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1. MING-JEN LEE; Su Y.N.; You H.L.; Chiou S.C.; Lin L.C.; Yang C.C.; Lee W.C.; Hwu W.L.; Hsieh F.J.; Stephenson D.A.; Yu C.L.
臺大學術典藏 2020-03-03T02:33:35Z Six novel NPC1 mutations in Chinese patients with Niemann-Pick disease type C Yang C.-C.; Su Y.-N.; Chiou P.-C.; Fietz M.J.; Yu C.-L.; Hwu W.-L.; MING-JEN LEE
臺大學術典藏 2020-03-03T01:14:51Z DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients Wang C.K; Wu Y.R; Hwu W.L; Chen C.M; Ro L.S; Chen S.T; Gwinn-Hardy K; Yang C.C; Wu R.M; TA-FU CHEN; Wang H.C; Chao M.C; Chiu M.J; Lu C.J; Lee-Chen G.J.
臺大學術典藏 2020-02-27T01:50:09Z Human pompe disease-induced pluripotent stem cells for pathogenesis modeling, drug testing and disease marker identification Huang H.-P.;Chen P.-H.;Hwu W.-L.;Chuang C.-Y.;Chien Y.-H.;Stone L.;Chung-Liang Chien;Li L.-T.;Chiang S.-C.;Chen H.-F.;Ho H.-N.;Chen C.-H.;Kuo H.-C.; Huang H.-P.; Chen P.-H.; Hwu W.-L.; Chuang C.-Y.; Chien Y.-H.; Stone L.; CHUNG-LIANG CHIEN; Li L.-T.; Chiang S.-C.; Chen H.-F.; Ho H.-N.; Chen C.-H.; Kuo H.-C.
臺大學術典藏 2020-02-27T01:50:09Z Human Pompe disease-induced pluripotent stem cells for pathogenesis modeling, drug testing and disease marker identification Huang H.-P. ;Chen P.-H. ;Hwu W.-L. ;Chuang C.-Y. ;Chien Y.-H. ;Stone L. ;Chung-Liang Chien ;Li L.-T. ;Chiang S.-C. ;Chen H.-F. ;Ho H.-N. ;Chen C.-H. ;Kuo H.-C.; Huang H.-P.; Chen P.-H.; Hwu W.-L.; Chuang C.-Y.; Chien Y.-H.; Stone L.; CHUNG-LIANG CHIEN; Li L.-T.; Chiang S.-C.; Chen H.-F.; Ho H.-N.; Chen C.-H.; Kuo H.-C.
臺大學術典藏 2020-02-26T07:30:05Z Electrical abnormalities in dopaminergic neurons of the substantia nigra in mice with an aromatic L-amino acid decarboxylase deficiency Ho S.-Y; Chien Y.-H; Tsai L.-K; Muramatsu S.-I; Hwu W.-L; HORNG-HUEI LIOU; Lee N.-C.
臺大學術典藏 2020-02-25T08:01:46Z Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and Parkin gene mutations Ruey-Meei Wu;Shan D.-E;Sun C.-M;Liu R.-S;Hwu W.-L;Tai C.-H;Hussey J;West A;Gwinn-Hardy K;Hardy J;Chen J;Farrer M;Lincoln S.; RUEY-MEEI WU; Shan D.-E; Sun C.-M; Liu R.-S; Hwu W.-L; Tai C.-H; Hussey J; West A; Gwinn-Hardy K; Hardy J; Chen J; Farrer M; Lincoln S.
臺大學術典藏 2020-02-25T08:01:45Z DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients Wang C.K;Wu Y.R;Hwu W.L;Chen C.M;Ro L.S;Chen S.T;Gwinn-Hardy K;Yang C.C;Ruey-Meei Wu;Chen T.F;Wang H.C;Chao M.C;Chiu M.J;Lu C.J;Lee-Chen G.J.; Wang C.K; Wu Y.R; Hwu W.L; Chen C.M; Ro L.S; Chen S.T; Gwinn-Hardy K; Yang C.C; RUEY-MEEI WU; Chen T.F; Wang H.C; Chao M.C; Chiu M.J; Lu C.J; Lee-Chen G.J.
臺大學術典藏 2020-02-25T08:01:44Z Parkin mutations and early-onset parkinsonism in a Taiwanese cohort Ruey-Meei Wu;Bounds R;Lincoln S;Hulihan M;Lin C.-H;Hwu W.-L;Chen J;Gwinn-Hardy K;Farrer M.; RUEY-MEEI WU; Bounds R; Lincoln S; Hulihan M; Lin C.-H; Hwu W.-L; Chen J; Gwinn-Hardy K; Farrer M.

Showing items 596-605 of 770  (77 Page(s) Totally)
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