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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 26, 2026
A real-world study on the treatment of pediatric narcolepsy with pitolisant in China
Shen Zhang, Yun Wu, Weihua Zhang, et al.
Life Sciences
|
October 9, 2025
Targeting ferroptosis and mitochondrial abnormalities: a promising therapeutic strategy for diabetes and its complications
Huayuan Liu, Chen Zhang, Jiuwei Li, et al.
European Journal of Medical Genetics
|
February 2, 2021
Novel truncating mutations in ASXL1 identified in two boys with Bohring-Opitz syndrome
Jianbo Zhao, Yanqi Hou, Fang Fang, et al.
Multiple Sclerosis and Related Disorders
|
September 12, 2022
Mycophenolate mofetil: An alternative disease-modifying agent for MOG-IgG-associated disorders in childhood: A single-center bidirectional cohort study
Ji Zhou, Jiuwei Li, Changhong Ren, et al.
Epilepsia
|
December 22, 2025
The symmetrical claustrum sign in pediatric febrile infection-related epilepsy syndrome: Diagnostic value and clinical implications
Xiaodi Han, Changhong Ren, Hua Cheng, et al.
Pediatric Investigation
|
April 6, 2022
Chinese patients with p.Arg756 mutations of <i>ATP1A3</i>: Clinical manifestations, treatment, and follow-up
Weihua Zhang, Jiuwei Li, Xiuwei Zhuo, et al.
Scientific Reports
|
October 24, 2017
Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type A
Xiaozhu Wang, Yu Huang, Ming Yan, et al.
Developmental Medicine and Child Neurology
|
September 15, 2022
Clinical and genetic spectrum of hereditary spastic paraplegia in Chinese children
Jiaping Wang, Fang Fang, Changhong Ding, et al.
Clinical Genetics
|
October 11, 2025
Genotype-Phenotype Correlations in Chinese Pediatric Patients With Single Large-Scale Mitochondrial DNA Deletion Disorders
Jun Wang, Minhan Song, Zhimei Liu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 20, 2018
Lack of association between valproic acid response and polymorphisms of its metabolism, transport, and receptor genes in children with focal seizures
Weixing Feng, Shenghui Mei, Jiaqi Han, et al.
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of 5
Search research articles
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Showing results (21-30 of 45) with videos related to
Sort By:
Page
of 5
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 26, 2026
A real-world study on the treatment of pediatric narcolepsy with pitolisant in China
Shen Zhang, Yun Wu, Weihua Zhang, et al.
Life Sciences
|
October 9, 2025
Targeting ferroptosis and mitochondrial abnormalities: a promising therapeutic strategy for diabetes and its complications
Huayuan Liu, Chen Zhang, Jiuwei Li, et al.
European Journal of Medical Genetics
|
February 2, 2021
Novel truncating mutations in ASXL1 identified in two boys with Bohring-Opitz syndrome
Jianbo Zhao, Yanqi Hou, Fang Fang, et al.
Multiple Sclerosis and Related Disorders
|
September 12, 2022
Mycophenolate mofetil: An alternative disease-modifying agent for MOG-IgG-associated disorders in childhood: A single-center bidirectional cohort study
Ji Zhou, Jiuwei Li, Changhong Ren, et al.
Epilepsia
|
December 22, 2025
The symmetrical claustrum sign in pediatric febrile infection-related epilepsy syndrome: Diagnostic value and clinical implications
Xiaodi Han, Changhong Ren, Hua Cheng, et al.
Pediatric Investigation
|
April 6, 2022
Chinese patients with p.Arg756 mutations of <i>ATP1A3</i>: Clinical manifestations, treatment, and follow-up
Weihua Zhang, Jiuwei Li, Xiuwei Zhuo, et al.
Scientific Reports
|
October 24, 2017
Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type A
Xiaozhu Wang, Yu Huang, Ming Yan, et al.
Developmental Medicine and Child Neurology
|
September 15, 2022
Clinical and genetic spectrum of hereditary spastic paraplegia in Chinese children
Jiaping Wang, Fang Fang, Changhong Ding, et al.
Clinical Genetics
|
October 11, 2025
Genotype-Phenotype Correlations in Chinese Pediatric Patients With Single Large-Scale Mitochondrial DNA Deletion Disorders
Jun Wang, Minhan Song, Zhimei Liu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 20, 2018
Lack of association between valproic acid response and polymorphisms of its metabolism, transport, and receptor genes in children with focal seizures
Weixing Feng, Shenghui Mei, Jiaqi Han, et al.
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of 5