Case report: A rare homozygous variation in the ENPP1 gene, presenting with generalized arterial calcification of infancy in a Chinese infant

por Lu, Pengtao, Chen, Jinglong, Chen, Mei, Wang, Ling, Xiang, Dandan, Yin, Jie, Yang, Shiwei
Publicado 2023

Rapid hydrogel formation via tandem visible light photouncaging and bioorthogonal ligation

por Chung, Kun-You, Halwachs, Kathleen N., Lu, Pengtao, Sun, Kaihong, Silva, Hope A., Rosales, Adrianne M., Page, Zachariah A.
Publicado 2022

Case report: Rare novel MIPEP compound heterozygous variants presenting with hypertrophic cardiomyopathy, severe lactic acidosis and hypotonia in a Chinese infant

por Wang, Ling, Lu, Pengtao, Yin, Jie, Xu, Kangkang, Xiang, Dandan, Zhang, Zhongman, Zhang, Han, Zheng, Bixia, Zhou, Wei, Wang, Chunli, Yang, Shiwei
Publicado 2023

Clinical characteristics and survival of children with hypertrophic cardiomyopathy in China: A multicentre retrospective cohort study

por Chan, Wenxiu, Yang, Shiwei, Wang, Jian, Tong, Shilu, Lin, Minyin, Lu, Pengtao, Yao, Ruen, Wu, Lanping, Chen, Lijun, Guo, Ying, Shen, Jie, Liu, Tingliang, Li, Fen, Chen, Huiwen, Zhang, Hao, Wang, Shushui, Fu, Lijun
Publicado 2022