Chunxi Han

Congenital muscular dystrophies in China

Ge Lin, Cheng Zhang, Zhaoxia Wang et al. · Clinical Genetics · 2019 · 49 citations

Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients

Danyu Song, Yi Dai, Xiaoyu Chen et al. · Clinical Genetics · 2020 · 37 citations

Initial application of three-dimensional speckle-tracking echocardiography to detect subclinical left ventricular dysfunction and stratify cardiomyopathy associated with Duchenne muscular dystrophy in children

Hong-kui Yu, Bei Xia, Xiao Liu et al. · International journal of cardiac imaging · 2018 · 31 citations

Three-dimensional Speckle-tracking Echocardiography, Heart Failure, Cardiomyopathy +12

Clinical and MRI features of neurological complications after influenza A (H1N1) infection in critically ill children

Hongwu Zeng, Stephen Quinet, Wenxian Huang et al. · Pediatric Radiology · 2013 · 30 citations

Clinical Neurology, Pediatrics, Mri Features +9

FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies

Xiaona Fu, Haipo Yang, Cuijie Wei et al. · Journal of Human Genetics · 2016 · 19 citations · Full text

Founder Mutation, Mendelian Disorder, Fkrp Mutations +8