Mutant EXT1 in Taiwanese Patients with Multiple Hereditary Exostoses

by Lin, Wei-De, Hwu, Wuh-Liang, Wang, Chung-Hsing, Tsai, Fuu-Jen
Published 2014

RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia

by Lin, Wei-De, Lin, Shuan-Pei, Wang, Chung-Hsing, Tsai, Yushin, Chen, Chih-Ping, Tsai, Fuu-Jen
Published 2011

Successful control with carbamazepine of family with paroxysmal kinesigenic dyskinesia of PRRT2 mutation

by Chou, I-Ching, Lin, Sheng-Shing, Lin, Wei-De, Wang, Chung-Hsing, Chang, Yu-Tzu, Tsai, Fuu-Jen, Tsai, Chang-Hai
Published 2014

Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB

by Chang, Yu-Tzu, Wang, Chung-Hsing, Chou, I-Ching, Lin, Wei-De, Chee, Siew-Yin, Kuo, Huang-Tsung, Tsai, Fuu-Jen
Published 2014

Long-term galsulfase enzyme replacement therapy in Taiwanese mucopolysaccharidosis VI patients: A case series

by Lin, Hsiang-Yu, Chuang, Chih-Kuang, Wang, Chung-Hsing, Chien, Yin-Hsiu, Wang, Yu-Mei, Tsai, Fuu-Jen, Chou, Yen-Yin, Lin, Shio Jean, Pan, Hui-Ping, Niu, Dau-Ming, Hwu, Wuh-Liang, Ke, Yu-Yuan, Lin, Shuan-Pei
Published 2016