Publications by authors named "Chunxi Han"

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Research on Constitutive Modeling of DH460 Continuous Casting Steel with the Solidification End Reduction Process.
Bochun Liang, Chunxi Han, Tan Zhao, Cheng Ji, Miaoyong Zhu

Materials (Basel)· January 2025

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Novel Intronic Mutations Introduce Pseudoexons in DMD That Cause Muscular Dystrophy in Patients.
Xinguo Lu, Chunxi Han, Jiahui Mai, Xianping Jiang, Jianxiang Liao

Front Genet· April 2021

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Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients.
Danyu Song, Yi Dai, Xiaoyu Chen, Xiaona Fu, Xingzhi Chang, Cheng Zhang, Chunxi Han

Clin Genet· March 2021

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c.3G>A mutation in the gene that causes fatal infantile hypertonic myofibrillar myopathy in the Chinese population.
Xin-Guo Lu, Uet Yu, Chun-Xi Han, Jia-Hui Mai, Jian-Xiang Liao

J Integr Neurosci· March 2021

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Congenital muscular dystrophies in China.
Lin Ge, Cheng Zhang, Zhaoxia Wang, Sophelia H S Chan, Wenhua Zhu, Chunxi Han, Xiaoli Zhang, Jingli Shan, Xingzhi Chang, Yuehua Zhang

Clin Genet· September 2019

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A mutation in the filamin c gene causes myofibrillar myopathy with lower motor neuron syndrome: a case report.
Juanjuan Chen, Jun Wu, Chunxi Han, Yao Li, Yuzu Guo

BMC Neurol· August 2019

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Effectiveness of High-Speed T2-Corrected Multiecho MR Spectroscopic Method for Quantifying Thigh Muscle Fat Content in Boys With Duchenne Muscular Dystrophy.
Zhiyong Li, Hongwu Zeng, Chunxi Han, Longwei Sun, Diangang Fang

AJR Am J Roentgenol· June 2019

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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, Chunxi Han, Weiling Chen

Int J Cardiovasc Imaging· January 2019

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FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies.
Xiaona Fu, Haipo Yang, Cuijie Wei, Hui Jiao, Shuo Wang, Chunxi Han

J Hum Genet· December 2016

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Mutation in the caveolin-3 gene causes asymmetrical distal myopathy.
Juanjuan Chen, Wenshuang Zeng, Chunxi Han, Jun Wu, Haiou Zhang

Neuropathology· October 2016

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Patient with spinal muscular atrophy with respiratory distress type 1 presenting initially with hypertonia.
Chunxi Han, Jiahui Mai, Tian Tian, Yanxia He, Jianxiang Liao

Brain Dev· May 2015

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[A novel mutation in GCH1 gene causes dopa-responsive dystonia].
Weiqing Wu, Chunxi Han, Ying Hao, Jiansheng Xie, Zhiyong Xu

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· August 2014

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Clinical and MRI features of neurological complications after influenza A (H1N1) infection in critically ill children.
Hongwu Zeng, Stephen Quinet, Wenxian Huang, Yungen Gan, Chunxi Han

Pediatr Radiol· September 2013

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[Genetic analysis and prenatal diagnosis for a family with megalencephalic leukoencephalopathy and subcortical cysts].
Wei-qing Wu, Jian-sheng Xie, Chun-xi Han, Zhi-yong Xu, Qian Geng

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· December 2011

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CA2: the most vulnerable sector to bicuculline exposure in rat hippocampal slice cultures.
Chunxi Han, Nahoko Kasai, Keiichi Torimitsu

Neuroreport· March 2005

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Detection of glutamate in optically trapped single nerve terminals by Raman spectroscopy.
Katsuhiro Ajito, Chunxi Han, Keiichi Torimitsu

Anal Chem· May 2004

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