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Showing items 181-205 of 221  (9 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2018-09-10T04:17:00Z Distributions of p53 codon 72 polymorphism in primary open angle glaucoma Lin, H.-J.;Chen, W.-C.;Tsai, F.-J.;Tsai, S.-W.; SHIH-WEI TSAI
臺大學術典藏 2018 Temporal and Reciprocal Relations Between ADHD symptoms and Emotional Problems in School-Age Children Han G.T.; Chen Y.-L.; Tsai F.-J.; SUSAN SHUR-FEN GAU
臺大學術典藏 2018 Functional independence of Taiwanese children with Prader–Willi syndrome Lee C.-L.;Lin H.-Y.;Tsai L.-P.;Chiu H.-C.;Tu R.-Y.;Huang Y.-H.;Chien Y.-H.;Ni-Chung Lee;Niu D.-M.;Chao M.-C.;Tsai F.-J.;Chou Y.-Y.;Chuang C.-K.;Lin S.-P.; Lee C.-L.; Lin H.-Y.; Tsai L.-P.; Chiu H.-C.; Tu R.-Y.; Huang Y.-H.; Chien Y.-H.; NI-CHUNG LEE; Niu D.-M.; Chao M.-C.; Tsai F.-J.; Chou Y.-Y.; Chuang C.-K.; Lin S.-P.
臺大學術典藏 2018 Clinical characteristics and surgical history of Taiwanese patients with mucopolysaccharidosis type II: Data from the hunter outcome survey (HOS) Lin H.-Y.; Chuang C.-K.; Chen M.-R.; Lin S.J.; Chiu P.C.; Niu D.-M.; Tsai F.-J.; Hwu W.-L.; YIN-HSIU CHIEN; Lin J.-L.; Lin S.-P.
國立成功大學 2018 Functional independence of Taiwanese children with Prader–Willi syndrome Lee, C.-L.;Lin, H.-Y.;Tsai, L.-P.;Chiu, H.-C.;Tu, R.-Y.;Huang, Y.-H.;Chien, Y.-H.;Lee, N.-C.;Niu, D.-M.;Chao, M.-C.;Tsai, F.-J.;Chou, Y.-Y.;Chuang, Chuang C.-K.;Lin, S.-P.
臺大學術典藏 2016 Causes of death and clinical characteristics of 34 patients with Mucopolysaccharidosis II in Taiwan from 1995-2012 Dr. Segolene Ayme Lin H.-Y.; Chuang C.-K.; Huang Y.-H.; Tu R.-Y.; Lin F.-J.; Lin S.J.; Chiu P.C.; Niu D.-M.; Tsai F.-J.; Hwu W.-L.; YIN-HSIU CHIEN; Lin J.-L.; Chou Y.-Y.; Tsai W.-H.; Chang T.-M.; Lin S.-P.
臺大學術典藏 2016 Long-term galsulfase enzyme replacement therapy in Taiwanese mucopolysaccharidosis VI patients: A case series Lin H.-Y.; Chuang C.-K.; Wang C.-H.; YIN-HSIU CHIEN; Wang Y.-M.; Tsai F.-J.; Chou Y.-Y.; Lin S.J.; Pan H.-P.; Niu D.-M.; Hwu W.-L.; Ke Y.-Y.; Lin S.-P.
國立臺灣大學 2015 TET2 ALTERATIONS IN TAIWANESE CHILDHOOD ACUTE MYELOID LEUKEMIA Li, M. J.; Lin, D. T.; Tsai, F. J.; Tsai, C. H.; Peng, C. T.; 李孟儒; 林東燦
臺大學術典藏 2015 Long-term prognosis of patients with infantile-onset pompe disease diagnosed by newborn screening and treated since birth Hwu W.-L.; Hsu W.-C.; Tsai T.-H.; Chien Y.-H.; Huang H.-J.; JENG-YI SHIEH; Lee N.-C.; Chen C.-A.; Tsai F.-J.; Tsai W.-H.
臺大學術典藏 2015 Long-term prognosis of patients with infantile-onset pompe disease diagnosed by newborn screening and treated since birth Tsai W.-H.; Shieh J.-Y.; Tsai F.-J.; CHUN-AN CHEN; Lee N.-C.; Chien Y.-H.; Chien Y.-H.;Lee N.-C.;Chun-An Chen;Tsai F.-J.;Tsai W.-H.;Shieh J.-Y.;Huang H.-J.;Hsu W.-C.;Tsai T.-H.;Hwu W.-L.; Huang H.-J.; Hsu W.-C.; Tsai T.-H.; Hwu W.-L.
國立交通大學 2014-12-08T15:13:46Z Mutation analysis of the tumor suppressor gene PPP2R1B in human cervical cancer Yeh, L.-S.; Hsieh, Y.-Y.; Chang, J.-G.; Chang, W. W.-C.; Chang, C.-C.; Tsai, F.-J.
臺大學術典藏 2014 Mutant EXT1 in Taiwanese patients with multiple hereditary exostoses Lin W.-D.; WUH-LIANG HWU; Wang C.-H.; Tsai F.-J.
臺大學術典藏 2014 Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index Yamamoto K.; Kubo M.; Guo X.; Delahanty R.; Guo X.; Sheu W.H.-H.; Liang J.; Zhang Y.; He M.; Wu Y.; He J.; Wen W.; Zheng W.; Okada Y.; Takeuchi F.; Tabara Y.; Hwang J.-Y.; Dorajoo R.; Li H.; Tsai F.-J.; Yang X.; Chen C.-H.; Ong R.T.; Lu L.; Cho Y.S.; Takashima N.; Akiyama K.; Tsunoda T.; Long J.; Lee I.-T.; Ohkubo T.; Go M.J.; Liu J.J.; Gan W.; Chen C.-C.; Gao Y.; Li S.; Lee N.R.; Wu C.; Zhou X.; Song H.; Yao J.; Lee J.; Lim W.-Y.; Nabika T.; Lu W.; Sim X.; Kim B.-J.; Isono M.; Xiang Y.-B.; Hixson J.; Seielstad M.; Tan A.; Rice T.K.; Adair L.S.; Gui L.; Allison M.; Lee W.-J.; Cai Q.; Isomura M.; Umemura S.; Kim Y.J.; Young T.L.; Shin D.H.; Lee Y.-H.; Ji B.-T.; Lee J.; Shin M.-H.; Wang T.-D.; Lim W.Y.; Gao Y.-T.; Takayanagi R.; Kang D.-H.; Wong T.Y.; Hsiung C.A.; Wu I.-C.; JYH-MING JIMMY JUANG; Shi J.; Choi B.Y.; Aung T.; Hu F.; Kim M.K.; Mo Z.; Mohlke K.L.; Gu D.; Wu T.; Zhu D.; Qi L.; Rotter J.I.; Chun B.-Y.; Cho M.-C.; Han B.-G.; Hwu C.-M.; Assimes T.L.; Absher D.; Yan X.; Kim E.; Kuo J.Z.; Kwon S.; Taylor K.D.; Chen Y.-D.I.; Wu J.-Y.; Lin X.; Miki T.; Tai E.S.; Lee J.-Y.; Kato N.; Shu X.-O.; Tanaka T.
臺大學術典藏 2013 Erratum: Enzyme replacement therapy for mucopolysaccharidosis VI - Experience in Taiwan (Journal of Inherited Metabolic Disease DOI: 10.1007/s20545-101-9212-5) Lin H.-Y.; Chen M.-R.; Chuang C.-K.; Chen C.-P.; Lin D.-S.; Chien Y.-H.; Ke Y.-Y.; Tsai F.-J.; Pan H.-P.; Lin S.-J.; Hwu W.-L.; Niu D.-M.; NI-CHUNG LEE; Lin S.-P.
臺大學術典藏 2013 ADHD-related symptoms, emotional/behavioral problems, and physical conditions in Taiwanese children with epilepsy WANG-TSO LEE; Lee C.-M.; Tsai F.-J.; Liu S.-T.; Fan P.-C.; Lin W.-S.; Chiu Y.-N.; Gau S.S.F.
臺大學術典藏 2013 Molecular aspects of Dravet syndrome patients in Taiwan Wang C.-H.; Chang K.-P.; Lin W.-D.; Chen S.-J.; Fan P.-C.; WEN-CHIN WENG; Lin W.-C.; Tsai Y.; Tsai C.-H.; Chou I.-C.; Tsai F.-J.
臺大學術典藏 2013 erratum: Enzyme replacement therapy for mucopolysaccharidosis VI - Experience in Taiwan (Journal of Inherited Metabolic Disease DOI: 10.1007/s20545-101-9212-5) Lin H.-Y.; Chen M.-R.; Chuang C.-K.; Chen C.-P.; Lin D.-S.; YIN-HSIU CHIEN; Ke Y.-Y.; Tsai F.-J.; Pan H.-P.; Lin S.-J.; Hwu W.-L.; Niu D.-M.; Lee N.-C.; Lin S.-P.
臺大學術典藏 2011 Attentional processes and ADHD-related symptoms in pediatric patients with epilepsy Liu S.-T.;Tsai F.-J.;Lee W.-T.;Lee C.-M.;Fan P.-C.;Lin W.-S.;Chiu Y.-N.;Susan Shur-Fen Gau; Liu S.-T.; Tsai F.-J.; Lee W.-T.; Lee C.-M.; Fan P.-C.; Lin W.-S.; Chiu Y.-N.; SUSAN SHUR-FEN GAU
臺大學術典藏 2011 Impact of shock wave lithotripsy on heart rate variability in patients with urolithiasis Lin W.-C. ;Ho C.-Y. ;Chen Y.-H. ;Chen I.-C. ;Chen H.-Y. ;Tsai F.-J. ;Shen J.-L. ;Man S.S. ;Huang P.-H. ;Yuh-Lien Chen ;Man K.-M. ;Chen W.-C.; Lin W.-C.; Ho C.-Y.; Chen Y.-H.; Chen I.-C.; Chen H.-Y.; Tsai F.-J.; Shen J.-L.; Man S.S.; Huang P.-H.; YUH-LIEN CHEN; Man K.-M.; Chen W.-C.
臺大學術典藏 2011 Attentional processes and ADHD-related symptoms in pediatric patients with epilepsy Liu S.-T.;Tsai F.-J.;Lee W.-T.;Lee C.-M.;Pi-Chuan Fan;Lin W.-S.;Chiu Y.-N.;Gau S.S.F.; Liu S.-T.; Tsai F.-J.; Lee W.-T.; Lee C.-M.; PI-CHUAN FAN; Lin W.-S.; Chiu Y.-N.; Gau S.S.F.
臺大學術典藏 2011 Attentional processes and ADHD-related symptoms in pediatric patients with epilepsy Liu S.-T. ;Tsai F.-J. ;Wang-Tso Lee ;Lee C.-M. ;Fan P.-C. ;Lin W.-S. ;Chiu Y.-N. ;Gau S.S.F.; Liu S.-T.; Tsai F.-J.; WANG-TSO LEE; Lee C.-M.; Fan P.-C.; Lin W.-S.; Chiu Y.-N.; Gau S.S.F.
亞洲大學 2010-09 The NBS1 Genetic Polymorphisms and the Risk of the Systemic Lupus Erythematosus in Taiwanese Patients ;Lin, Y.J.;Lan, Y.C.;萬磊;Wan, Lei;Huang, C.M.;Lin, C.W.;Hsueh, K.C.;Chen, D.Y.;Lin, T.H.;Tsai, F.J.
亞洲大學 2010-08 Disease Association of the CD103 Polymorphisms in Taiwan Chinese Graves' Ophthalmopathy Patients ;Liu, Y.H.;Chen, R.H.;Chen, W.C.;Tsai, Y.;萬磊;Wan, Lei;Tsai, F.J.
亞洲大學 2010-06 The association between lumican gene polymorphisms and high myopia ;Lin, H.J.;萬磊;Wan, Lei;Tsai, Y.;Chen, W.C.;Tsai, S.W.;Tsai, F.J.
亞洲大學 2010-01 Association of the lumican gene functional 3'-UTR polymorphism with high myopia ;Lin, H.J.;Kung, Y.J.;Lin, Y.J.;Sheu, J.J.;Chen, B.H.;Lan, Y.C.;Lai, C.H.;Hsu, Y.A.;萬磊;Wan, Lei;Tsai, F.J.

Showing items 181-205 of 221  (9 Page(s) Totally)
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