| 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. |
| 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 |
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. |
| 國立臺灣大學 |
2012 |
A whole genome methylation analysis of systemic lupus erythematosus: hypomethylation of the IL10 and IL1R2 promoters is associated with disease activity
|
Lin, S-Y; Hsieh, S-C; Lin, Y-C; Lee, C-N; Tsai, M-H; Lai, L-C; Chuang, E. Y.; Chen, P-C; Hung, C-C; Chen, L-Y; Hsieh, W. S.; Niu, D-M; Su, Y-N; Ho, H-N; 陳保中; 謝武勳; 謝松洲 |
| 元培科技大學 |
2011-06 |
Idiopathic Calcinosis Cutis in a Child: Chemical Composition of the Calcified Deposits
|
Niu, D.-M.; Lin, S.-Y.; Li, M.-J.; Cheng, W.-T.; Pan, C.-C.; Lin, C.-C. |
| 臺大學術典藏 |
2009 |
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome
|
Su Y.;Niu D.-M;Ho H.-N;Cheng W.-F;Chiu H.-H;Yu C.-C;Lin C.-Y;Chang C.-H;Chen C.-P;Chen M.-R;Lin S.-P;Cheng H.-Y;CHIEN-NAN LEE;Lin S.-Y;Hung C.-C; Hung C.-C; Lin S.-Y; CHIEN-NAN LEE; Cheng H.-Y; Lin S.-P; Chen M.-R; Chen C.-P; Chang C.-H; Lin C.-Y; Yu C.-C; Chiu H.-H; Cheng W.-F; Ho H.-N; Niu D.-M; Su Y. |
