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Showing items 16-40 of 69  (3 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2021-05-26T09:08:05Z Distinct clinical and biologic characteristics in adult acute myeloid leukemia bearing the isocitrate dehydrogenase 1 mutation Chou W.-C.; Hou H.-A.; Chen C.-Y.; Tang J.-L.; Yao M.; Tsay W.; Ko B.-S.; Wu S.-J.; Huang S.-Y.; Hsu S.-C.; YAO-CHANG CHEN; Huang Y.-N.; Chang Y.-.; Lee F.-Y.; Liu M.-C.; Liu C.-W.; Tseng M.-H.; Huang C.-F.; Tien H.-F.
臺大學術典藏 2021-05-26T09:08:04Z Distinct clinical and biological features of de novo acute myeloid leukemia with additional sex comb-like 1 (ASXL1) mutations Chou W.-C.; Huang H.-H.; Hou H.-A.; Chen C.-Y.; Tang J.-L.; Yao M.; Tsay W.; Ko B.-S.; Wu S.-J.; Huang S.-Y.; Hsu S.-C.; YAO-CHANG CHEN; Huang Y.-N.; Chang Y.-C.; Lee F.-Y.; Liu M.-C.; Liu C.-W.; Tseng M.-H.; Huang C.-F.; Tien H.-F.
臺大學術典藏 2021-05-19T01:57:28Z Acute myeloid leukemia bearing t(7;11)(p15;p15) is a distinct cytogenetic entity with poor outcome and a distinct mutation profile: Comparative analysis of 493 adult patients Chou W.-C.; Chen C.-Y.; Hou H.-A.; Lin L.-I.; Tang J.-L.; Yao M.; Tsay W.; Ko B.-S.; Wu S.-J.; Huang S.-Y.; SZU-CHUN HSU; Chen Y.-C.; Huang Y.-N.; Tseng M.-H.; Huang C.-F.; Tien H.-F.
臺大學術典藏 2021-05-19T01:57:26Z Distinct clinical and biologic characteristics in adult acute myeloid leukemia bearing the isocitrate dehydrogenase 1 mutation Chou W.-C.; Hou H.-A.; Chen C.-Y.; Tang J.-L.; Yao M.; Tsay W.; Ko B.-S.; Wu S.-J.; Huang S.-Y.; SZU-CHUN HSU; Chen Y.-C.; Huang Y.-N.; Chang Y.-.; Lee F.-Y.; Liu M.-C.; Liu C.-W.; Tseng M.-H.; Huang C.-F.; Tien H.-F.
臺大學術典藏 2021-05-19T01:57:24Z Distinct clinical and biological features of de novo acute myeloid leukemia with additional sex comb-like 1 (ASXL1) mutations Chou W.-C.; Huang H.-H.; Hou H.-A.; Chen C.-Y.; Tang J.-L.; Yao M.; Tsay W.; Ko B.-S.; Wu S.-J.; Huang S.-Y.; SZU-CHUN HSU; Chen Y.-C.; Huang Y.-N.; Chang Y.-C.; Lee F.-Y.; Liu M.-C.; Liu C.-W.; Tseng M.-H.; Huang C.-F.; Tien H.-F.
臺大學術典藏 2021-03-08T08:06:11Z A case of GNE myopathy mimicking hereditary motor neuropathy Huang Y.-N.;Chuang H.-J.;Hsueh H.-W.;Huang H.-C.;Lee N.-C.;Chao C.-C.;Huang P.-H.;Lee Y.-C.;Lin K.-P.;Yang C.-C.;Sung-Tsang Hsieh; Huang Y.-N.; Chuang H.-J.; Hsueh H.-W.; Huang H.-C.; Lee N.-C.; Chao C.-C.; Huang P.-H.; Lee Y.-C.; Lin K.-P.; Yang C.-C.; SUNG-TSANG HSIEH
臺大學術典藏 2021-03-05T08:48:35Z A case of GNE myopathy mimicking hereditary motor neuropathy Huang, Y-N;Chuang, H-J;Hsueh, H-W;Huang, H-C;Lee, N-C;Chao, C-C;Pei-Hsin Huang;Lee, Y-C;Lin, K-P;Yang, C-C;Hsieh, S-T; Huang, Y-N; Chuang, H-J; Hsueh, H-W; Huang, H-C; Lee, N-C; Chao, C-C; PEI-HSIN HUANG; Lee, Y-C; Lin, K-P; Yang, C-C; Hsieh, S-T
臺大學術典藏 2021-02-05T06:29:45Z Acute myeloid leukemia bearing t(7;11)(p15;p15) is a distinct cytogenetic entity with poor outcome and a distinct mutation profile: Comparative analysis of 493 adult patients Wen-Chien Chou;Chen C.-Y.;Hou H.-A.;Lin L.-I.;Tang J.-L.;Yao M.;Tsay W.;Ko B.-S.;Wu S.-J.;Huang S.-Y.;Hsu S.-C.;Chen Y.-C.;Huang Y.-N.;Tseng M.-H.;Huang C.-F.;Tien H.-F.; WEN-CHIEN CHOU; Chen C.-Y.; Hou H.-A.; Lin L.-I.; Tang J.-L.; Yao M.; Tsay W.; Ko B.-S.; Wu S.-J.; Huang S.-Y.; Hsu S.-C.; Chen Y.-C.; Huang Y.-N.; Tseng M.-H.; Huang C.-F.; Tien H.-F.
臺大學術典藏 2021-02-05T06:29:44Z Distinct clinical and biologic characteristics in adult acute myeloid leukemia bearing the isocitrate dehydrogenase 1 mutation Wen-Chien Chou;Hou H.-A.;Chen C.-Y.;Tang J.-L.;Yao M.;Tsay W.;Ko B.-S.;Wu S.-J.;Huang S.-Y.;Hsu S.-C.;Chen Y.-C.;Huang Y.-N.;Chang Y.-.;Lee F.-Y.;Liu M.-C.;Liu C.-W.;Tseng M.-H.;Huang C.-F.;Tien H.-F.; WEN-CHIEN CHOU; Hou H.-A.; Chen C.-Y.; Tang J.-L.; Yao M.; Tsay W.; Ko B.-S.; Wu S.-J.; Huang S.-Y.; Hsu S.-C.; Chen Y.-C.; Huang Y.-N.; Chang Y.-.; Lee F.-Y.; Liu M.-C.; Liu C.-W.; Tseng M.-H.; Huang C.-F.; Tien H.-F.
臺大學術典藏 2021-02-05T06:29:43Z A single-tube, sensitive multiplex method for screening of isocitrate dehydrogenase 1 (IDH1) mutations Wen-Chien Chou;Huang Y.-N.;Huang C.-F.;Tseng M.-H.;Tien H.-F.; WEN-CHIEN CHOU; Huang Y.-N.; Huang C.-F.; Tseng M.-H.; Tien H.-F.
臺大學術典藏 2021-02-05T06:29:42Z Distinct clinical and biological features of de novo acute myeloid leukemia with additional sex comb-like 1 (ASXL1) mutations Wen-Chien Chou;Huang H.-H.;Hou H.-A.;Chen C.-Y.;Tang J.-L.;Yao M.;Tsay W.;Ko B.-S.;Wu S.-J.;Huang S.-Y.;Hsu S.-C.;Chen Y.-C.;Huang Y.-N.;Chang Y.-C.;Lee F.-Y.;Liu M.-C.;Liu C.-W.;Tseng M.-H.;Huang C.-F.;Tien H.-F.; WEN-CHIEN CHOU; Huang H.-H.; Hou H.-A.; Chen C.-Y.; Tang J.-L.; Yao M.; Tsay W.; Ko B.-S.; Wu S.-J.; Huang S.-Y.; Hsu S.-C.; Chen Y.-C.; Huang Y.-N.; Chang Y.-C.; Lee F.-Y.; Liu M.-C.; Liu C.-W.; Tseng M.-H.; Huang C.-F.; Tien H.-F.
臺大學術典藏 2021-02-05T06:29:40Z Sensitive measurement of quantity dynamics of FLT3 internal tandem duplication at early time points provides prognostic information Wen-Chien Chou;Hou H.-A.;Liu C.-Y.;Chen C.-Y.;Lin L.-I.;Huang Y.-N.;Chao Y.-C.;Hsu C.-A.;Huang C.-F.;Tien H.-F.; WEN-CHIEN CHOU; Hou H.-A.; Liu C.-Y.; Chen C.-Y.; Lin L.-I.; Huang Y.-N.; Chao Y.-C.; Hsu C.-A.; Huang C.-F.; Tien H.-F.
臺大學術典藏 2021-01-12T12:49:20Z Acute myeloid leukemia bearing t(7;11)(p15;p15) is a distinct cytogenetic entity with poor outcome and a distinct mutation profile: Comparative analysis of 493 adult patients Chou W.-C.; Chen C.-Y.; Hou H.-A.; Lin L.-I.; Tang J.-L.; Yao M.; Tsay W.; Ko B.-S.; Wu S.-J.; SHANG-YI HUANG; Hsu S.-C.; Chen Y.-C.; Huang Y.-N.; Tseng M.-H.; Huang C.-F.; Tien H.-F.
臺大學術典藏 2021-01-12T12:49:19Z Distinct clinical and biologic characteristics in adult acute myeloid leukemia bearing the isocitrate dehydrogenase 1 mutation Wu S.-J.; Ko B.-S.; Yao M.; Tsay W.; Chen C.-Y.; Tang J.-L.; Hou H.-A.; Chou W.-C.; SHANG-YI HUANG; Hsu S.-C.; Chen Y.-C.; Huang Y.-N.; Chang Y.-.; Lee F.-Y.; Liu M.-C.; Liu C.-W.; Tseng M.-H.; Huang C.-F.; Tien H.-F.
臺大學術典藏 2021-01-12T12:49:17Z Distinct clinical and biological features of de novo acute myeloid leukemia with additional sex comb-like 1 (ASXL1) mutations Huang Y.-N.; Chen Y.-C.; Wu S.-J.; SHANG-YI HUANG; Hsu S.-C.; Chou W.-C.; Huang H.-H.; Hou H.-A.; Chen C.-Y.; Tang J.-L.; Yao M.; Tsay W.; Ko B.-S.; Chang Y.-C.; Lee F.-Y.; Liu M.-C.; Liu C.-W.; Tseng M.-H.; Huang C.-F.; Tien H.-F.
臺大學術典藏 2021-01-06T03:58:45Z Acute myeloid leukemia bearing t(7;11)(p15;p15) is a distinct cytogenetic entity with poor outcome and a distinct mutation profile: Comparative analysis of 493 adult patients Chou W.-C.; Chen C.-Y.; Hou H.-A.; Lin L.-I.; JIH-LUH TANG; Yao M.; Tsay W.; Ko B.-S.; Wu S.-J.; Huang S.-Y.; Hsu S.-C.; Chen Y.-C.; Huang Y.-N.; Tseng M.-H.; Huang C.-F.; Tien H.-F.
臺大學術典藏 2021-01-06T03:58:42Z Distinct clinical and biologic characteristics in adult acute myeloid leukemia bearing the isocitrate dehydrogenase 1 mutation Liu M.-C.; Chou W.-C.; Hou H.-A.; Chen C.-Y.; JIH-LUH TANG; Yao M.; Tsay W.; Ko B.-S.; Wu S.-J.; Huang S.-Y.; Hsu S.-C.; Chen Y.-C.; Huang Y.-N.; Chang Y.-.; Lee F.-Y.; Liu C.-W.; Tseng M.-H.; Huang C.-F.; Tien H.-F.
臺大學術典藏 2021-01-06T03:58:41Z Distinct clinical and biological features of de novo acute myeloid leukemia with additional sex comb-like 1 (ASXL1) mutations Chou W.-C.; Huang H.-H.; Hou H.-A.; Chen C.-Y.; JIH-LUH TANG; Yao M.; Tsay W.; Ko B.-S.; Wu S.-J.; Huang S.-Y.; Hsu S.-C.; Chen Y.-C.; Huang Y.-N.; Chang Y.-C.; Lee F.-Y.; Liu M.-C.; Liu C.-W.; Tseng M.-H.; Huang C.-F.; Tien H.-F.
臺大學術典藏 2021-01-05T03:34:50Z Distinct clinical and biologic characteristics in adult acute myeloid leukemia bearing the isocitrate dehydrogenase 1 mutation Chen C.-Y.; Hou H.-A.; Chou W.-C.; Huang Y.-N.; Hsu S.-C.; Chen Y.-C.; Huang S.-Y.; Wu S.-J.; Ko B.-S.; MING YAO; Tsay W.; Tang J.-L.; Tien H.-F.; Huang C.-F.; Tseng M.-H.; Liu C.-W.; Liu M.-C.; Chang Y.-.; Lee F.-Y.
臺大學術典藏 2021-01-05T03:34:48Z Distinct clinical and biological features of de novo acute myeloid leukemia with additional sex comb-like 1 (ASXL1) mutations Huang S.-Y.; Hsu S.-C.; Wu S.-J.; Ko B.-S.; Tsay W.; MING YAO; Chou W.-C.; Huang H.-H.; Hou H.-A.; Chen C.-Y.; Tang J.-L.; Chang Y.-C.; Huang Y.-N.; Chen Y.-C.; Tien H.-F.; Huang C.-F.; Tseng M.-H.; Liu M.-C.; Liu C.-W.; Lee F.-Y.
臺大學術典藏 2021-01-05T00:56:42Z Acute myeloid leukemia bearing t(7;11)(p15;p15) is a distinct cytogenetic entity with poor outcome and a distinct mutation profile: Comparative analysis of 493 adult patients Hsu S.-C.; Huang S.-Y.; SHANG-JU WU; Ko B.-S.; Tsay W.; Chou W.-C.; Chen C.-Y.; Hou H.-A.; Lin L.-I.; Tang J.-L.; Yao M.; Chen Y.-C.; Huang Y.-N.; Tseng M.-H.; Huang C.-F.; Tien H.-F.
國立成功大學 2021 Collapse seismic risk assessment for irregular mid-rise buildings Lu, Lu L.-Y.;Hsiao, F.-P.;Huang, Y.-N.;Hsieh, W.-H.
臺大學術典藏 2020-12-10T01:24:26Z A case of GNE myopathy mimicking hereditary motor neuropathy Huang, Y-N;Chuang, H-J;Hsueh, H-W;Huang, H-C;Ni-Chung Lee;Chao, C-C;Huang, P-H;Lee, Y-C;Lin, K-P;Yang, C-C;Hsieh, S-T; Huang, Y-N; Chuang, H-J; Hsueh, H-W; Huang, H-C; NI-CHUNG LEE; Chao, C-C; Huang, P-H; Lee, Y-C; Lin, K-P; Yang, C-C; Hsieh, S-T
臺大學術典藏 2020-11-11T07:58:22Z A case of GNE myopathy mimicking hereditary motor neuropathy Huang Y.-N.; Chuang H.-J.; HSUEH-WEN HSUEH; Huang H.-C.; Lee N.-C.; Chao C.-C.; Huang P.-H.; Lee Y.-C.; Lin K.-P.; Yang C.-C.; Hsieh S.-T.
臺大學術典藏 2020-11-03T10:54:58Z A case of GNE myopathy mimicking hereditary motor neuropathy Yang C.-C.; Hsieh S.-T.; Lin K.-P.; Lee Y.-C.; Lee N.-C.; CHI-CHAO CHAO; Huang P.-H.; Huang Y.-N.;Chuang H.-J.;Hsueh H.-W.;Huang H.-C.;Lee N.-C.;Chi-Chao Chao;Huang P.-H.;Lee Y.-C.;Lin K.-P.;Yang C.-C.;Hsieh S.-T.; Huang H.-C.; Hsueh H.-W.; Chuang H.-J.; Huang Y.-N.

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