Chunxi Han

机构：Shenzhen Children's Hospital

发表论文 26 篇 · 总被引 237 次 · h-index 8

代表论文

• Congenital muscular dystrophies in China (2019 · Clinical Genetics · 被引 52)
• Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients (2020 · Clinical Genetics · 被引 42)
• Initial application of three-dimensional speckle-tracking echocardiography to detect subclinical left ventricular dysfunction and stratify cardiomyopathy associated with Duchenne muscular dystrophy in children (2018 · International journal of cardiac imaging · 被引 34)
• Clinical and MRI features of neurological complications after influenza A (H1N1) infection in critically ill children (2013 · Pediatric Radiology · 被引 30)
• FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies (2016 · Journal of Human Genetics · 被引 20)
• A mutation in the filamin c gene causes myofibrillar myopathy with lower motor neuron syndrome: a case report (2019 · BMC Neurology · 被引 14)