Qiong-xiang Zhai

发表

Mutations in the sodium channel genes SCN1A, SCN3A, and SCN9A in children with epilepsy with febrile seizures plus(EFS+)

Hongxia Ma, Yu-xiong Guo, Zhi-hong Chen, 2021, Seizure.

Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy

Xin Li, Xin Li, Xiao-Rong Liu, 2022, Frontiers in Molecular Neuroscience.

Children treated for epileptic encephalopathies show improved glucose metabolism

J. Gui, Qiong-xiang Zhai, H. Qiao, 2010, Pediatrics international : official journal of the Japan Pediatric Society.

Mutational analysis of CHRNB 2 , CHRNA 2 and CHRNA 4 genes in Chinese population with autosomal dominant nocturnal frontal lobe epilepsy

Yu-xiong Guo, Zhi-hong Chen, Lingan Wang, 2015 .

Analysis of the CHRNA7 gene mutation and polymorphism in Southern Han Chinese patients with nocturnal frontal epilepsy.

Yu-xiong Guo, Zhi-hong Chen, Lingan Wang, 2015, Asian Pacific journal of tropical medicine.

Whole-Exome Sequencing for Identifying Genetic Causes of Intellectual Developmental Disorders

Yu-xiong Guo, Zhi-hong Chen, Qiong-xiang Zhai, 2021, International journal of general medicine.

A novel missense creatine mutant of CaBP4, c.464G>A (p.G155D), associated with autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE), reduces the expression of CaBP4

X. Li, Yu-xiong Guo, Zhi-hong Chen, 2022, Translational pediatrics.

ATP6V0C Is Associated With Febrile Seizures and Epilepsy With Febrile Seizures Plus

Zhen Shi, W. Liao, Xiao-jing Li, 2022, Frontiers in Molecular Neuroscience.

Novel mutations in SCN9A occurring with fever-associated seizures or epilepsy

Yu-xiong Guo, Zhi-hong Chen, Jing-wen Zhang, 2019, Seizure.

BCOR variants are associated with X-linked recessive partial epilepsy

Xiao-Rong Liu, W. Liao, N. He, 2022, Epilepsy Research.

Etiological and clinical analysis on 220 children with cerebrovascular diseases

Zhi-hong Tang, Qiong-xiang Zhai, Chun Wang, 2014 .

Novel KCNQ 4 gene mutations contribute to susceptibility of genetic febrile seizures

Lingan Wang, Jing-wen Zhang, Qiong-xiang Zhai, 2016 .

Research of the serum level of neuron-specific enolase in children with various types of seizure

Zhi-hong Tang, Qiong-xiang Zhai, Chun Wang, 2012 .

Scalp EEG high frequency oscillations as a biomarker of treatment response in epileptic encephalopathy with continuous spike-and-wave during sleep (CSWS)

Hiroki Nariai, F. Wen, Yan Chen, 2019, Seizure.

Chloroquine inhibits autophagy and deteriorates the mitochondrial dysfunction and apoptosis in hypoxic rat neurons☆

Guang Yang, P. Li, Lei Hao, 2018, Life sciences.

DEPDC5 Variants Associated Malformations of Cortical Development and Focal Epilepsy With Febrile Seizure Plus/Febrile Seizures: The Role of Molecular Sub-Regional Effect

Xiao-Rong Liu, W. Liao, N. He, 2020, Frontiers in Neuroscience.

Original Article A novel ARSA gene mutation c.302delG in a Chinese patient with metachromatic leukodystrophy

Yu-xiong Guo, Zhi-hong Chen, Lingan Wang, 2016 .

A novel ARSA gene mutation c . 302 delG in a Chinese patient with metachromatic leukodystrophy

Yu-xiong Guo, Zhi-hong Chen, Lingan Wang, 2016 .

MED12 variants associated with X-linked recessive partial epilepsy without intellectual disability

M. Zhang, N. He, Zhigang Liu, 2023, Seizure.

Novel mutations and phenotypes of epilepsy‐associated genes in epileptic encephalopathies

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2018, Genes, brain, and behavior.

[Effect of Ilepcimide Combined Western Drugs on Serum Level of Neuron Specific Enolase in Treating Epilepsy Children Patients].

Yu-xiong Guo, Zhi-hong Chen, Lingan Wang, 2016, Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine.

Characteristics of very high frequency oscillations of somatosensory evoked potentials in humans with epilepsy

Y. Inoue, K. Terada, K. Matsuda, 2014 .

Efficacy and safety of switching from brand-name to domestic generic levetiracetam in children with epilepsy.

Zhi-hong Chen, Jing-wen Zhang, Qiong-xiang Zhai, 2022, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

Correlation between interictal cerebral glucose hypometabolism and IQ in children with epilepsy

Zhi-hong Chen, Zhi-hong Tang, Qiong-xiang Zhai, 2014, Epilepsy & Behavior.

HCFC1 variants in the proteolysis domain are associated with X‐linked idiopathic partial epilepsy: Exploring the underlying mechanism

B. Tang, D. Zhou, Yi-wu Shi, 2023, Clinical and translational medicine.

Recessive APC2 missense variants associated with epilepsies without neurodevelopmental disorders

Yun Li, N. He, Jianhang Guo, 2023, Seizure: European Journal of Epilepsy.

Exome sequencing identified a novel missense mutation c.464G>A (p.G155D) in Ca2+-binding protein 4 (CABP4) in a Chinese pedigree with autosomal dominant nocturnal frontal lobe epilepsy

J. Gui, Yu-xiong Guo, Zhi-hong Chen, 2017, Oncotarget.

DYNC1H1 variants associated with infant-onset epilepsy without neurodevelopmental disorders

W. Liao, N. He, Zhigang Liu, 2023, Seizure: European Journal of Epilepsy.

ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes

W. Liao, N. He, Yong-Hong Yi, 2024, Journal of Medical Genetics.

DYNC1H1 variants associated with infant-onset epilepsy without neurodevelopmental disorders

W. Liao, N. He, Zhigang Liu, 2023, Seizure: European Journal of Epilepsy.

Children treated for epileptic encephalopathies show improved glucose metabolism

J. Gui, Qiong-xiang Zhai, H. Qiao, 2010, Pediatrics international : official journal of the Japan Pediatric Society.