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Safety and efficacy of teriflunomide in paediatric multiple sclerosis (TERIKIDS): a multicentre, double-blind, phase 3, randomised, placebo-controlled trial

Lancet neurology, 2021-12, Vol.20 (12), p.1001-1011

2021

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Novel NtA and LG1 Mutations in Agrin in a Single Patient Causes Congenital Myasthenic Syndrome

Frontiers in neurology, 2020-04, Vol.11, p.239

2020

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Early-onset epileptic encephalopathy with de novo SCN8A mutation

Epilepsy research, 2018-01, Vol.139, p.9-13

2018

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MicroRNA-34b mediates hippocampal astrocyte apoptosis in a rat model of recurrent seizures

BMC neuroscience, 2016-08, Vol.17 (1), p.56-56, Article 56

2016

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Clinicopathological characteristics of dysplastic teratomous neuroglia with anti-N-methyl-d-aspartate receptor encephalitis

Clinical immunology (Orlando, Fla.), 2020-01, Vol.210, p.108271-108271, Article 108271

2020

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Identification of Biomarkers Associated With CD4+ T-Cell Infiltration With Gene Coexpression Network in Dermatomyositis

Frontiers in immunology, 2022-05, Vol.13, p.854848-854848

2022

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NLRC5: A Potential Target for Central Nervous System Disorders

Frontiers in immunology, 2021-06, Vol.12, p.704989-704989

2021

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Neuroprotection of cannabidiol in epileptic rats: Gut microbiome and metabolome sequencing

Frontiers in nutrition (Lausanne), 2022-11, Vol.9, p.1028459-1028459

2022

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Case Report: Evidences of myasthenia and cerebellar atrophy in a chinese patient with novel compound heterozygous MSTO1 variants

Frontiers in genetics, 2022-08, Vol.13

2022

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Effects of Rhizoma Acori Tatarinowii extracts on gamma-aminobutyric acid type A receptor alpha 1 subunit brain expression during development in a recurrent seizure rat model

Neural regeneration research, 2011-02, Vol.6 (6), p.412-417

Liqun Liu Ding＇an Mao Keqiang Chi Xingfang Li Tao Bo Jinming Guo Zhuwen Yi

2011

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Case Report: Aicardi-Goutières Syndrome Type 6 and Dyschromatosis Symmetrica Hereditaria With Congenital Heart Disease and Mitral Valve Calcification – Phenotypic Variants Caused by Adenosine Deaminase Acting on the RNA 1 Gene Homozygous Mutations

Frontiers in pediatrics, 2022-06, Vol.10

2022

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The Clinical, Radiologic, and Prognostic Differences Between Pediatric and Adult Patients With Myelin Oligodendrocyte Glycoprotein Antibody-Associated Encephalomyelitis

Frontiers in neurology, 2021-05, Vol.12, p.679430-679430

2021

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The First Case Report of X-Linked Sideroblastic Anemia With Ataxia of Chinese Origin and Literature Review

Frontiers in pediatrics, 2021-07, Vol.9

2021

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Case Report: A case of recurrent thrombosis in pediatric antiphospholipid syndrome associated with pediatric onset systemic lupus

Frontiers in pediatrics, 2023-02, Vol.10, p.1004053

2023

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Analysis of Clinical and Genetic Characterization of Three Ataxia-Telangiectasia Pedigrees With Novel ATM Gene Mutations

Frontiers in pediatrics, 2022-05, Vol.10, p.877826-877826

2022

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Clinical characteristics of anti - N - methyl - D - aspartate receptor encephalitis in children

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2020-01, Vol.45 (1), p.47-54

2020

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Effects of progesterone on glutamate transporter 2 and gamma-aminobutyric acid transporter 1 expression in the developing rat brain after recurrent seizures

Neural regeneration research, 2012-09, Vol.7 (26), p.2036-2042

2012

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Construction of a Prognostic Gene Signature Associated with Immune Infiltration in Glioma: A Comprehensive Analysis Based on the CGGA

Journal of oncology, 2021, Vol.2021, p.6620159-19

2021

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Novel NtA and LG1 Mutations in Agrin in a Single Patient Causes Congenital Myasthenic Syndrome

Frontiers in neurology, 2020, Vol.11, p.239-239

2020

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Effects of progesterone on glutamate transporter 2 and gamma-aminobutyric acid transporter 1 expression in the developing rat brain after recurrent seizures

Neural regeneration research, 2012-09, Vol.7 (25), p.2036-2042

2012

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Case Report: Evidences of myasthenia and cerebellar atrophy in a chinese patient with novel compound heterozygous MSTO1 variants

Frontiers in genetics, 2022, Vol.13, p.947886-947886

2022

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Case Report: Aicardi-Goutières Syndrome Type 6 and Dyschromatosis Symmetrica Hereditaria With Congenital Heart Disease and Mitral Valve Calcification - Phenotypic Variants Caused by Adenosine Deaminase Acting on the RNA 1 Gene Homozygous Mutations

Frontiers in pediatrics, 2022, Vol.10, p.852903-852903

2022

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The First Case Report of X-Linked Sideroblastic Anemia With Ataxia of Chinese Origin and Literature Review

Frontiers in pediatrics, 2021, Vol.9, p.692459-692459

2021

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Case Report: A case of recurrent thrombosis in pediatric antiphospholipid syndrome associated with pediatric onset systemic lupus

Frontiers in pediatrics, 2022, Vol.10, p.1004053-1004053

2022

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The PER3rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria

Journal of molecular medicine (Berlin, Germany), 2023-03, Vol.101 (3), p.279-294

2023

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Safety and efficacy of teriflunomide in paediatric multiple sclerosis (TERIKIDS): a multicentre, double-blind, phase 3, randomised, placebo-controlled trial

Novel NtA and LG1 Mutations in Agrin in a Single Patient Causes Congenital Myasthenic Syndrome

Early-onset epileptic encephalopathy with de novo SCN8A mutation

MicroRNA-34b mediates hippocampal astrocyte apoptosis in a rat model of recurrent seizures

Clinicopathological characteristics of dysplastic teratomous neuroglia with anti-N-methyl-d-aspartate receptor encephalitis

Identification of Biomarkers Associated With CD4+ T-Cell Infiltration With Gene Coexpression Network in Dermatomyositis

NLRC5: A Potential Target for Central Nervous System Disorders

Neuroprotection of cannabidiol in epileptic rats: Gut microbiome and metabolome sequencing

Case Report: Evidences of myasthenia and cerebellar atrophy in a chinese patient with novel compound heterozygous MSTO1 variants

Effects of Rhizoma Acori Tatarinowii extracts on gamma-aminobutyric acid type A receptor alpha 1 subunit brain expression during development in a recurrent seizure rat model

Case Report: Aicardi-Goutières Syndrome Type 6 and Dyschromatosis Symmetrica Hereditaria With Congenital Heart Disease and Mitral Valve Calcification – Phenotypic Variants Caused by Adenosine Deaminase Acting on the RNA 1 Gene Homozygous Mutations

The Clinical, Radiologic, and Prognostic Differences Between Pediatric and Adult Patients With Myelin Oligodendrocyte Glycoprotein Antibody-Associated Encephalomyelitis

The First Case Report of X-Linked Sideroblastic Anemia With Ataxia of Chinese Origin and Literature Review

Case Report: A case of recurrent thrombosis in pediatric antiphospholipid syndrome associated with pediatric onset systemic lupus

Analysis of Clinical and Genetic Characterization of Three Ataxia-Telangiectasia Pedigrees With Novel ATM Gene Mutations

Clinical characteristics of anti - N - methyl - D - aspartate receptor encephalitis in children

Effects of progesterone on glutamate transporter 2 and gamma-aminobutyric acid transporter 1 expression in the developing rat brain after recurrent seizures

Construction of a Prognostic Gene Signature Associated with Immune Infiltration in Glioma: A Comprehensive Analysis Based on the CGGA

Novel NtA and LG1 Mutations in Agrin in a Single Patient Causes Congenital Myasthenic Syndrome

Effects of progesterone on glutamate transporter 2 and gamma-aminobutyric acid transporter 1 expression in the developing rat brain after recurrent seizures

Case Report: Evidences of myasthenia and cerebellar atrophy in a chinese patient with novel compound heterozygous MSTO1 variants

Case Report: Aicardi-Goutières Syndrome Type 6 and Dyschromatosis Symmetrica Hereditaria With Congenital Heart Disease and Mitral Valve Calcification - Phenotypic Variants Caused by Adenosine Deaminase Acting on the RNA 1 Gene Homozygous Mutations

The First Case Report of X-Linked Sideroblastic Anemia With Ataxia of Chinese Origin and Literature Review

Case Report: A case of recurrent thrombosis in pediatric antiphospholipid syndrome associated with pediatric onset systemic lupus

The PER3rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria

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