公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2004 | DNA haplotype analysis of CAG repeat in Taiwanese Huntington’s disease patients | Wang, CK; Wu, YR; Hwu, WL; Chen, CM; Ro, LS; Chen, ST; Gwinn-Hardy, K; Yang, CC; Wu, RM; Chen, TF; Wang, HC; Chao, MC; Chiu, MJ; Lu, CJ; Lee-Chen, GJ | Eur Neurol | | | |
2006 | Hepatic steatosis and neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) in Taiwanese infants. | Yeh, JN; Jeng, YM; Chen, HL; Ni, YH; Hwu, WL; Chang, MH. | J Pediatr | | | |
2008 | 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 | J Neurol | | | |
2008 | Long-term follow-up of a girl with Maroteaux-Lamy syndrome after bone marrow transplantation. | Wang, CC; Hwu, WL; Lin, KH. | World J Pediatr | | | |
2007 | Treatment of Niemann-Pick disease type C in two children with miglustat: Initial responses and maintenance of effects over 1 year. | Chien, YH; Lee, NC; Tsai, LK; Huang, AC; Peng, SF; Chen, SJ; Hwu, WL | J Inherit Metab Dis | | | |