Association Between Methylmalonic Acid and Cognition: A Systematic Review and Meta-Analysis

por Wang, Chao, Zhang, Ying, Shu, Jianbo, Gu, Chunyu, Yu, Yuping, Liu, Wei
Publicado 2022

The biallelic novel pathogenic variants in AGL gene in a chinese patient with glycogen storage disease type III

por Wang, Jing, Yu, Yuping, Cai, Chunquan, Zhi, Xiufang, Zhang, Ying, Zhao, Yu, Shu, Jianbo
Publicado 2022

Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report

por Wu, Jinying, Lei, Meifang, Wang, Xuetao, Liu, Nan, Xu, Xiaowei, Gu, Chunyu, Yu, Yuping, Liu, Wei
Publicado 2023

Efficacy and Safety of Diet Therapies in Children With Autism Spectrum Disorder: A Systematic Literature Review and Meta-Analysis

por Yu, Yuping, Huang, Jinyue, Chen, Xiaofang, Fu, Jia, Wang, Xinhui, Pu, Linjie, Gu, Chunyu, Cai, Chunquan
Publicado 2022

Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report

por Wu, Jinying, Lei, Meifang, Wang, Xuetao, Liu, Nan, Xu, Xiaowei, Gu, Chunyu, Yu, Yuping, Liu, Wei
Publicado 2022

Identification of a Novel Deep Intronic Variant by Whole Genome Sequencing Combined With RNA Sequencing in a Chinese Patient With Menkes Disease

por Zhi, Xiufang, Ai, Qi, Sheng, Wenchao, Yu, Yuping, Shu, Jianbo, Yu, Changshun, Yu, Xiaoli, Li, Dong, Cai, Chunquan
Publicado 2022