公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
---|---|---|---|---|---|---|
2004 | Association of aspirin with eosinophilia in peripheral blood [4] | Cheng T.-I.; TSUN-JEN CHENG ; Chiang S.C. | Annals of Pharmacotherapy | 4 | 4 | |
2013 | Endothelin type A receptor genotype is a determinant of quantitative traits of metabolic syndrome in Asian hypertensive families: A SAPPHIRe study | Ho L.T.; Hsu Y.P.; Hsiao C.F.; Ting C.T.; Shih K.C.; LEE-MING CHUANG ; Masaki K.; Grove J.; Quertermous T.; Juan C.C.; Lin M.W.; Chiang S.C.; Chen Y.D.I. | Frontiers in Endocrinology | 3 | 0 | |
2012 | Fabry disease: incidence of the common later-onset α-galactosidase A IVS4+919G→A mutation in Taiwanese newborns--superiority of DNA-based to enzyme-based newborn screening for common mutations. | YIN-HSIU CHIEN ; NI-CHUNG LEE ; Chiang S.C.; Desnick R.J.; WUH-LIANG HWU | Molecular medicine (Cambridge, Mass.) | 69 | 59 | |
2002 | Gemcitabine and cisplatin in a multimodality treatment for locally advanced non-small cell lung cancer | CHIH-HSIN YANG ; PAN-CHYR YANG ; Wang L.S.; Lee Y.C.; CHIEN-JEN CHANG ; Lui L.T.; Yen S.H.; CHIUN HSU ; ANN-LII CHENG ; Liu M.Y.; Chiang S.C.; Chen Y.M.; KWEN-TAY LUH ; Huang M.H.; Yang P.-C.; Perng R.-P. | British Journal of Cancer | 24 | 20 | |
2004 | Mutation spectrum in Taiwanese patients with phenylalanine hydroxylase deficiency and a founder effect for the R241C mutation. | YIN-HSIU CHIEN ; Chiang S.C.; Huang A.; Chou S.P.; Tseng S.S.; Huang Y.T.; WUH-LIANG HWU | Human mutation | 33 | 0 | |
2014 | Suboptimal duration of granulocyte colony-stimulating factor use and chemotherapy-induced neutropenia in women diagnosed with breast cancer | Lin W.-T.; Wen Y.-W.; Chien C.-R.; Gau C.-S.; Chiang S.C.; FEI-YUAN HSIAO | Clinical Therapeutics | 4 | 4 |