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Science China. Life Sciences|June 23, 2017
The clinical and genetic characteristics in children with mitochondrial disease in ChinaFang Fang, Zhimei Liu, Hezhi Fang, et al.
Science China. Life Sciences|July 22, 2017
Erratum to: The clinical and genetic characteristics in children with mitochondrial disease in ChinaFang Fang, Zhimei Liu, Hezhi Fang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 14, 2016
[Diagnosis of mitochondrial disorders in children with next generation sequencing]Zhimei Liu, Fang Fang, Changhong Ding, et al.
Brain : a Journal of Neurology|May 7, 2019
Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathiesCiria C Hernandez, Wenshu XiangWei, Ningning Hu, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 16, 2021
Age-dependent characteristics and prognostic factors of pediatric anti-N-methyl-d-aspartate receptor encephalitis in a Chinese single-center studyWeihua Zhang, Changhong Ren, Xiaohui Wang, et al.
Parkinsonism & Related Disorders|October 17, 2024
The clinical spectrum and pathogenesis associated with KMT2B variants in Chinese pediatric patientsShuangjin Ding, Gang Xie, Zonglin Han, et al.
Annals of Neurology|January 30, 2022
Leigh Syndrome: A Study of 209 Patients at the Beijing Children's HospitalSarah L Stenton, Ying Zou, Hua Cheng, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 18, 2026
The Movement Disorder Spectrum of ATP1A3-Related Disorders: Cross-Sectional Analysis and Video Archive of 88 PatientsKaterina Bernardi, Anna Zhou, Kathryn Yang, et al.
Brain : a Journal of Neurology|August 14, 2025
Molecular and clinical spectrum of epilepsy-dyskinesia syndromes: a cross-sectional study of 609 patientsVicente Quiroz, Julian E Alecu, Umar Zubair, et al.
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