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Frontiers in Neuroscience|June 30, 2026
A novel <i>de novo QRICH1</i> variant causing Ververi-Brady syndrome with infantile epileptic spasms syndrome: clinical and genetic analysisHongjun Fang, Xinghan Wu, Xiaojun Kuang, et al.
Frontiers in Neuroscience|June 5, 2023
Clinical spectrum of contactin-associated protein 2 autoimmune encephalitis in childrenWenjing Hu, Enhui Wang, Hongjun Fang, et al.
Optics Express|May 9, 2023
High-precision method for simultaneously measuring the six-degree-of-freedom relative position and pose deformation of satellitesFajia Zheng, Zhijia Liu, Fei Long, et al.
Frontiers in Neurology|January 4, 2024
Clinical characteristics and genetic analysis of pediatric patients with sodium channel gene mutation-related childhood epilepsy: a review of 94 patientsHongjun Fang, Wenjing Hu, Qingyun Kang, et al.
Frontiers in Neuroscience|January 9, 2023
Clinical and genetic analyses of premature mitochondrial encephalopathy with epilepsia partialis continua caused by novel biallelic <i>NARS2</i> mutationsWenjing Hu, Hongjun Fang, Yu Peng, et al.
Molecular Genetics & Genomic Medicine|October 19, 2022
Nabais Sa-de Vries syndrome in a Chinese infant associated with a novel SPOP mutation: A clinical study and genetic reportWenjing Hu, Hongjun Fang, Yu Peng, et al.
The International Journal of Neuroscience|April 22, 2020
The correlation of neutrophil-to-lymphocyte ratio with the presence and short-time curative effect of myasthenia gravis in children: a retrospectively studyZhi Jiang, Zeshu Ning, Liming Yang, et al.
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