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顯示項目151-175 / 232. (共10頁) << < 1 2 3 4 5 6 7 8 9 10 > >> 每頁顯示[10|25|50]項目

日期	題名	作者
2001-12	Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation	Wei-De Lin; Wu,Jer-Yuarn; Tsai,Fuu-Jen; Lee,Chun-Cheng; Chang-Hai Tsai
2006-02	Mutation Analysis of Crouzon Syndrome in Taiwanese Patients	Chin-Ping Chang; Lei Wan; Chang-Hai Tsai; Cheng-Chun Lee; Fuu-Jen Tsai
2006-05	Mutation analysis of Gaucher disease patients in Taiwan: high prevalence of the RecNciI and L444P mutations	Lei Wan; Hsu CM; Chang-Hai Tsai; Lee,Chun-Cheng; Hwu WL; Tsai,Fuu-Jen
2006-06	Mutation analysis of Taiwanese Wilson disease patients	Lei Wan; Chang-Hai Tsai; Yuhsin Tsai; Hsu CM; Lee,Chun-Cheng; Tsai,Fuu-Jen
2002	Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan	Shi YR; Wu,Jer-Yuarn; Hsu YA; Cheng-Chun Lee; Chang-Hai Tsai; Fuu-Jen Tsai
2003	Neurodevelopment outcome of meconium aspiration syndrome at 2 years of age	Lin Hung-Chih; Bai-Horng Su; Tsung-Wen Lin; Chang-Hai Tsai
1996	Neuroimaging of pediatric cerebral infarctions	Wu-Chung Shen; Chang-Hai Tsai; Su-Tso Yang
2005	No association between TAP1 Dpn2 polymorphism and bronchopulmonary dysplasia	Hung-Chih Lin; Bai-Horng Su; Chin-Moo Hsu; Kang-Hsi Wu; Hsiao-Chuan Lin; Fuu-Jen Tsai; Chang-Hai Tsai
2005-09	No Association between TAP1 DpnII Polymorphism and Bronchopulmonary Dysplasia	Hung-Chih Lin; Bai-Horng Su; Tsu-Fuh Yeh; Chang-Hai Tsai
2004-07	No association of p53 codon 72 and p21 codon 31 polymorphisms in Taiwan Chinese patients with pterygium	Yi-Yu Tsai; YW Cheng; Chiu-Yueh Lee; SH Tseng; Chang-Hai Tsai; Fuu-Jen Tsai
2004-11	No association of urokinase gene 3'-UTR polymorphism with bronchopulmonary dysplasia for ventilated preterm infants	Lin HC; Su BH; Lin TW; Hsu CM; Lei Wan; Chang-Hai Tsai; Fuu-Jen Tsai
2005-10	No relationship between -627 interleukin-10 promoter polymorphism in Chinese patients with rheumatoid arthritis	Chung-Ming Huang; Chang-Hai Tsai; Chi-Lan Chen; Chin-Ping Chang; Tsai,Fuu-Jen
2000	Normal Values of Inner Canthal Distance, Interpupillary Distance and Palpebral Fissure Length in Normal Chinese Children in Taiwan	Kang-Hsi Wu; Fuu-Jen Tsai; Tsai-Chung Li; Chang-Hai Tsai; Ching-Tien Peng; Tso-Ren Wang
2009-10	A Novel Strategy for Designing Dual-target Inhibitors of KU86 and XRCC4	Chien-Yu Chen; Fuu-Jen Tsai; Jing-Gung Chung; Chang-Hai Tsai; Yuan-Man Hsu; Hung-Jin Huang; Tin-Yun Ho; Yea-Huey Chang; Da-Tian Bau; Ming-Hsui Tsai; Chen, Calvin Yu-Chian
2005-03	Objective structured clinical examination (OSCE): A comparison of interpersonal skills scores with written part scores of OSCE	蘇百弘; 沈戊忠; 陳偉德; 洪瑞松; 蔡長海
2004-03	Outcomes at School Age after Postnatal Dexamethasone Therapy for Lung Disease of Prematurity	Tsu-Fuh Yeh; Yuh J. Lin; Lin Hung-Chih; Chao C. Huang; Wu S. Hsieh; CHIN-LIN CHANG; Chang-Hai Tsai
2009-03	The p21 codon 31( *)C- and DRD2 codon 313( *)T-related genotypes/alleles, but not XRCC1 codon 399, hOGG1 codon 326, and DRD1-48 polymorphisms, are correlated with the presence of leiomyoma	Hsieh Yao-Yuan; Chang CC; Da-Tian Bau; Fuu-Jen Tsai; Tsai CH; Chen CP
2001	p21 gene codon 31 arginine/serine polymorphism: Non-association with endometrosis	Hsieh Yao-Yuan; Fuu-Jen Tsai; Chang CC; Chen Wen-Chi; Chang-Hai Tsai; Tsai HD; Cheng-Chieh Lin
2008-03	p53 Codon 72 Proline/Arginine Polymorphism and Autoimmune Thyroid Diseases	Rong-Hsing Chen; Chwen-Tzuei Chang; Tzu-Yuan Wang; Wen-Liang Huang; Chang-Hai Tsai; Fuu-Jen Tsai
2006-11	Penil length of noormal boys in Taiwan	Wei-De Lin; Chang-Hai Tsai; Da-Tian Bau; Tsai,Fuu-Jen
2008-04	Pigment epithelium-derived factor gene Met72Thr polymorphism is associated with increased risk of wet age-related macular degeneration	Lin Jane-Ming; Lei Wan; Yi-Yu Tsai; Hui-Ju Lin; Yuhsin Tsai; Cheng-Chun Lee; Chang-Hai Tsai; SUNG-HUEI TSENG; Fuu-Jen Tsai
2001-07	A pilot study of neonatal screening by electrospray ionization tandem mass spectrometry in Taiwan	Wei-De Lin; Wu,Jer-Yuarn; Lai,Chien-Chen; Tsai,Fuu-Jen; Chang-Hai Tsai
2001-05	Pitfalls of PCR-based genotyping in patients with 21-hydroxylase deficiency	Chang-Hai Tsai; Wei-De Lin; Tsai,Fuu-Jen; Peng,Ching-Tien; Wu,Jer-Yuarn
2007-12	Polymorphism of XRCC1 Codon Arg 399 Gln Is Associated with Higher Susceptibility to Endometriosis	Da-Tian Bau; Hsieh Yao-Yuan; Lei Wan; Rou-Fen Wang; Chiu-Chu Liao; Cheng-Chun Lee; Cheng-Chieh Lin; Chang-Hai Tsai; Fuu-Jen Tsai
2002	Polymorphisms for interleukin 1 beta exon 5 and interleukin 1 receptor antagonist in Taiwanese children with febrile convulsions	Fuu-Jen Tsai; Hsieh Yao-Yuan; Chi-Chen Chang; Cheng-Chieh Lin; Chang-Hai Tsai

顯示項目151-175 / 232. (共10頁) << < 1 2 3 4 5 6 7 8 9 10 > >> 每頁顯示[10|25|50]項目