Growth Hormone Deficiency in a Case of Crouzon Syndrome with Hydrocephalus

por Wen, Mei-Hong, Hsiao, Hui-Pin, Chao, Mei-Chyn, Tsai, Fuu-Jen
Publicado 2010

Altered Pattern of Macrophage Polarization as a Biomarker for Severity of Childhood Asthma

por Kuo, Chang-Hung, Tsai, Mei-Lan, Li, Chung-Hsiang, Hsiao, Hui-Pin, Chao, Mei-Chyn, Lee, Ming-Sheng, Lin, Yi-Ching, Hung, Chih-Hsing
Publicado 2021

Epigenetic regulation of COX-2 expression by DNA hypomethylation via NF-κB activation in ketamine-induced ulcerative cystitis

por Chuang, Shu-Mien, Lu, Jian-He, Lin, Kun-Ling, Long, Cheng-Yu, Lee, Yung-Chin, Hsiao, Hui-Pin, Tsai, Chia-Chun, Wu, Wen-Jeng, Yang, Hui-Jun, Juan, Yung-Shun
Publicado 2019

Mutations in Pseudohypoparathyroidism 1a and Pseudopseudohypoparathyroidism in Ethnic Chinese

por Wu, Yi-Lei, Hwang, Daw-Yang, Hsiao, Hui-Pin, Ting, Wei-Hsin, Huang, Chi-Yu, Tsai, Wen-Yu, Chen, Hung-Chun, Chao, Mei-Chyn, Lo, Fu-Sung, Tsai, Jeng-Daw, Yang, Stone, Shih, Shin-Lin, Lin, Shuan-Pei, Lin, Chiung-Ling, Lee, Yann-Jinn
Publicado 2014

Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Beckwith-Wiedemann Syndrome

por Lin, Hsiang-Yu, Lee, Chung-Lin, Fran, Sisca, Tu, Ru-Yi, Chang, Ya-Hui, Niu, Dau-Ming, Chang, Chia-Ying, Chiu, Pao Chin, Chou, Yen-Yin, Hsiao, Hui-Pin, Yang, Chia-Feng, Tsai, Meng-Che, Chu, Tzu-Hung, Chuang, Chih-Kuang, Lin, Shuan-Pei
Publicado 2021

Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver–Russell Syndrome

por Lin, Hsiang-Yu, Lee, Chung-Lin, Fran, Sisca, Tu, Ru-Yi, Chang, Ya-Hui, Niu, Dau-Ming, Chang, Chia-Ying, Chiu, Pao-Chin, Chou, Yen-Yin, Hsiao, Hui-Pin, Tsai, Meng-Che, Chao, Mei-Chyn, Tsai, Li-Ping, Yang, Chia-Feng, Su, Pen-Hua, Pan, Yu-Wen, Lee, Chen-Hao, Chu, Tzu-Hung, Chuang, Chih-Kuang, Lin, Shuan-Pei
Publicado 2021