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Showing items 1-10 of 33  (4 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2018-09-10T06:49:59Z Early detection of pompe disease by newborn screening is feasible: Results from the Taiwan screening program Chien, YH;Chiang, SC;Zhang, XK;Keutzer, J;Lee, NC;Huang, AC;Chen, CA;Wu, MH;Huang, PH;Tsai, FJ;Chen, YT;Hwu, WL; Chien, Y.-H. and Chiang, S.-C. and Zhang, X.K. and Keutzer, J. and Lee, N.-C. and Huang, A.-C. and Chen, C.-A. and Wu, M.-H. and Huang, P.-H. and Tsai, F.-J. and Chen, Y.-T. and Hwu, W.-L.; CHUN-AN CHEN; Chien, YH; Chiang, SC; NI-CHUNG LEE; MEI-HWAN WU; Zhang, XK; YIN-HSIU CHIEN; Keutzer, J; WUH-LIANG HWU; Lee, NC; Huang, AC; PEI-HSIN HUANG; Chen, CA; Wu, MH; Huang, PH; Tsai, FJ; Chen, YT; Hwu, WL
臺大學術典藏 2018-09-10T06:12:49Z Computer simulation of hemodynamic changes after right lobectomy in a liver with intrahepatic portal vein aneurysm Ho, C.-M. and Tsai, S.-F. and Lin, R.-K. and Liang, P.-C. and Sheu, T.W.-H. and Hu, R.-H. and Lee, P.-H.; Sheu, Tony W. H.; Ho, C. M.; Tsai, S. F.; Lin, R. K.; Liang, P. C.; Hu, R. H.; Lee, P. H.; PO-HUANG LEE; Hsieh, CT; Sheu, Tony W. H.; PO-CHIN LIANG; Hwu, WL; Ho, C. M.; Huang, YT; REY-HENG HU; Tsai, S. F.; Lin, R. K.; CHENG-MAW HO; Huang, AC; Wang, SF; Liang, P. C.; Hu, MH; Hu, R. H.; Chien, YH.; Lee, P. H.
國立臺灣大學 2010 Phenotypic Analyses and Mutation Screening of the SLC26A4 and FOXI1 Genes in 101 Taiwanese Families with Bilateral Nonsyndromic Enlarged Vestibular Aqueduct (DFNB4) or Pendred Syndrome Wu, CC; Lu, YC; Chen, PJ; Yeh, PL; Su, YN; Hwu, WL; Hsu, CJ
國立臺灣大學 2009-04 Application of SNaPshot multiplex assays for simultaneous multigene mutation screening in patients with idiopathic sensorineural hearing impairment Wu, CC; Lu, YC; Chen, PJ; Liu, AY; Hwu, WL; Hsu, CJ
國立臺灣大學 2008-11 Brain Damage by Mild Metabolic Derangements in Methylmalonic Acidemia. Lee, NC; Chien, YH; Peng, SF; Huang, AC; Liu, TT; Wu, AS; Chen, LC; Hsu, LW; Tseng, SC; Hwu, WL.
國立臺灣大學 2008-07 Early detection of Pompe disease by newborn screening is feasible: results from the Taiwan screening program. Chien, YH; Chiang, SC; Zhang, XK; Keutzer, J; Lee, NC; Huang, AC; Chen, CA; Wu, MH; Huang, PH; Tsai, FJ; Chen, YT; Hwu, WL
亞洲大學 2008-05 Identification of eight novel mutations of the acid alpha-glucosidase gene causing the infantile or juvenile form of glycogen storage disease type II Lei Wan;Cheng-Chun Lee;Chin-Moo Hsu;Hwu WL;Yang CC;Chang-Hai Tsai;Fuu-Jen Tsai
國立臺灣大學 2008-05 Identification of eight novel mutations of the acid alpha-glucosidase gene causing the infantile or juvenile form of glycogen storage disease type II. Wan, L; Lee, CC; Hsu, CM; Hwu, WL; Yang, CC; Tsai, CH; Tsai, FJ
國立臺灣大學 2008-05 Long-term follow-up of a girl with Maroteaux-Lamy syndrome after bone marrow transplantation. Wang, CC; Hwu, WL; Lin, KH.
中國醫藥大學 2008-05 Identification of eight novel mutations of the acid alpha-glucosidase gene causing the infantile or juvenile form of glycogen storage disease type II. 萬磊(Lei Wan); 李正淳(Cheng-Chun Lee); 許欽木(Chin-Moo Hsu); (Hwu WL); (Yang CC); 蔡長海(Chang-Hai Tsai); 蔡輔仁(Fuu-Jen Tsai)*

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