Role of thyrotropin-releasing hormone test in re-evaluation of congenital hypothyroidism

by Li-Min Chen, Yen-Chun Chen, Hui-Pin Hsiao, Bai-Hsiun Chen, Mei-Chyn Chao
Published 2014-08-01

Novel SOX9 Gene Mutation in Campomelic Dysplasia with Autosomal Sex Reversal

by Hui-Pin Hsiao, Li-Ping Tsai, Mei-Chyn Chao, Hsin-I Tseng, Yuli C. Chang
Published 2006-01-01

Maternal diabetes or hypertension and lifestyle factors may be associated with metabolic syndrome: A population-based study in Taiwan

by Tzu-Hua Chen, Hui-Pin Hsiao, Yu-Wen Chiu, Nai-Hua Shih, Hung-Yi Chuang, Chia-Tsuan Huang
Published 2014-02-01

A Taiwanese Boy With Congenital Generalized Lipodystrophy Caused by Homozygous Ile262fs Mutation in the BSCL2 Gene

by Hsiu-Hui Huang, Tai-Heng Chen, Hui-Pin Hsiao, Chia-Tsuan Huang, Cheng-Chu Wang, Ya-Huei Shiau, Mei-Chyn Chao
Published 2010-11-01

1,2,3,4,6 penta-O-galloyl-β-D-glucose ameliorates high-fat diet-induced nonalcoholic fatty liver disease and maintains the expression of genes involved in lipid homeostasis in mice...

by Rajni Kant, Chung-Kuang Lu, Hien Minh Nguyen, Hui-Hua Hsiao, Chao-Ju Chen, Hui-Pin Hsiao, Kai-Jay Lin, Cheng-Chieh Fang, Chia-Hung Yen
Published 2020-09-01

Syndromic ciliopathy: a taiwanese single-center study

by Yu-Wen Pan, Tsung-Ying Ou, Yen-Yin Chou, Pao-Lin Kuo, Hui-Pin Hsiao, Pao-Chin Chiu, Ju-Li Lin, Fu-Sung Lo, Chung-Hsing Wang, Peng-Chieh Chen, Meng-Che Tsai
Published 2024-04-01

Congenital generalized lipodystrophy in Taiwan

by Rai-Hseng Hsu, Wei-De Lin, Mei-Chyn Chao, Hui-Pin Hsiao, Siew-Lee Wong, Pao-Chin Chiu, Shao-Yin Chu, Yu-Yuan Ke, Beng-Huat Lau, Yin-Hsiu Chien, Wuh-Liang Hwu, Fuu-Jen Tsai, Chung-Hsing Wang, Ni-Chung Lee
Published 2019-01-01

Mutations in pseudohypoparathyroidism 1a and pseudopseudohypoparathyroidism in ethnic Chinese.

by Yi-Lei Wu, Daw-Yang Hwang, Hui-Pin Hsiao, Wei-Hsin Ting, Chi-Yu Huang, Wen-Yu Tsai, Hung-Chun Chen, Mei-Chyn Chao, Fu-Sung Lo, Jeng-Daw Tsai, Stone Yang, Shin-Lin Shih, Shuan-Pei Lin, Chiung-Ling Lin, Yann-Jinn Lee
Published 2014-01-01

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

by Hsiang-Yu Lin, Chung-Lin Lee, Sisca Fran, Ru-Yi Tu, Ya-Hui Chang, Dau-Ming Niu, Chia-Ying Chang, Pao Chin Chiu, Yen-Yin Chou, Hui-Pin Hsiao, Chia-Feng Yang, Meng-Che Tsai, Tzu-Hung Chu, Chih-Kuang Chuang, Shuan-Pei Lin
Published 2021-10-01

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

by Hsiang-Yu Lin, Chung-Lin Lee, Sisca Fran, Ru-Yi Tu, Ya-Hui Chang, Dau-Ming Niu, Chia-Ying Chang, Pao-Chin Chiu, Yen-Yin Chou, Hui-Pin Hsiao, Meng-Che Tsai, Mei-Chyn Chao, Li-Ping Tsai, Chia-Feng Yang, Pen-Hua Su, Yu-Wen Pan, Chen-Hao Lee, Tzu-Hung Chu, Chih-Kuang Chuang, Shuan-Pei Lin
Published 2021-11-01