Echocardiographic characteristics of PRKAG2 syndrome: a research using three-dimensional speckle tracking echocardiography compared with sarcomeric hypertrophic cardiomyopathy

por Tang, Lu, Li, Xuejie, Zhou, Nianwei, Jiang, Yingying, Pan, Cuizhen, Shu, Xianhong
Publicado 2022

Whole-exome sequencing reveals a novel mutation of MT-ND5 gene in a mitochondrial cardiomyopathy pedigree: Patients who show biventricular hypertrophy, hyperlactacidemia, pulmonary...

por Zhou, Nianwei, Tang, Lu, Jiang, Yingying, Qin, Shengmei, Cui, Jie, Wang, Yanan, Zhu, Wenqing, Zhao, Weipeng, Pan, Cuizhen, Shu, Xianhong
Publicado 2019

A family with Danon disease caused by a splice site mutation in LAMP2 that generates a truncated protein

por Zhou, Nianwei, Cui, Jie, Zhao, Weipeng, Jiang, Yingying, Zhu, Wenqing, Tang, Lu, Li, Xuejie, Sun, Minmin, Pan, Cuizhen, Shu, Xianhong
Publicado 2019

The mechanical effects of CRT promoting autophagy via mitochondrial calcium uniporter down‐regulation and mitochondrial dynamics alteration

por Yu, Ziqing, Gong, Xue, Yu, Yong, Li, Minghui, Liang, Yixiu, Qin, Shengmei, Fulati, Zibire, Zhou, Nianwei, Shu, Xianhong, Nie, Zhenning, Dai, Shimo, Chen, Xueying, Wang, Jingfeng, Chen, Ruizhen, Su, Yangang, Ge, Junbo
Publicado 2019