Showing results (11-20 of 28) with videos related to
Sort By:
Pageof 3
Frontiers in Immunology|July 22, 2026
Epileptic spasms in the acute phase of pediatric anti-N-methyl-d-aspartate receptor encephalitis: a case seriesPingping Tian, Guiling Liu, Wandong Hu, et al.Human Mutation|July 28, 2026
Novel ALG13 Variants and an Expanded Neurodevelopmental Spectrum: Genotype-Phenotype CorrelationsSong Su, Wandong Hu, Ying Ren, et al.Medicine|January 10, 2025
De novo KCNB1 missense variant causing developmental and epileptic encephalopathy: Two case reportsYing Ren, Wandong Hu, Zaifen Gao, et al.Journal of Child Neurology|June 9, 2026
Superfast VNS Titration for the Treatment of SRSE in the Acute Phase of FIRES: A Pediatric Case Report and Literature ReviewYao Meng, Guifu Geng, Lin Wang, et al.Medicine|December 16, 2025
Severe anti-NMDA receptor encephalitis in a pediatric patient presenting with status dystonicus as the primary clinical manifestation: A case report (CARE)Pingping Tian, Juan Li, Meng Wang, et al.Frontiers in Allergy|March 2, 2026
Tic disorders and allergic diseases: mechanistic links and the impact of allergy management - a narrative reviewLili Li, Wandong Hu, Ying Ren, et al.Seizure|July 8, 2026
Genotype-phenotype correlations and clinical spectrum of ALG13-related developmental epileptic encephalopathySong Su, Wenchao Zhang, Ying Ren, et al.Epilepsia|June 20, 2026
Insights into ANKRD11-related epilepsy from 163 peopleSong Su, Jian Ma, Qi Zhang, et al.Medicine|August 2, 2024
Emphasis on the importance of comprehensive clinical and genetic analysis - spinal muscular atrophy combined with phenylketonuria: A case reportKai Ma, Dong Wang, Wandong Hu, et al.Seizure|November 6, 2025
Genotypic and phenotypic analysis of epilepsy associated with NPRL2/NPRL3 genesSong Su, Hongwei Zhang, Qi Zhang, et al.Pageof 3