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432 积分 2024-06-24 加入
Current and Emerging Precision Therapies for Developmental and Epileptic Encephalopathies
6天前
已完结
Phenotypic spectrum and genetics of SCN2A-related disorders, treatment options, and outcomes in epilepsy and beyond
6天前
已完结
Epileptic Encephalopathy with Variants in the PHACTR1 and AFF2 Genes: A Case Report
6天前
已完结
Challenges in seizure control in ATP6V0C deficiency: A longitudinal case report
6天前
已完结
Genetic analysis of developmental and epileptic encephalopathy caused by novel biallelic SZT2 gene mutations in three Chinese Han infants: a case series and literature review
6天前
已完结
Biallelic SZT2 variants in a child with developmental and epileptic encephalopathy
6天前
已完结
Novel West syndrome candidate genes in a Chinese cohort
6天前
已完结
[Clinical and genetic analysis of a child with West syndrome due to a de novo variant of NEXMIF gene]
6天前
已完结
Infantile spasms caused by NEXMIF mutation: A case report and literature review
6天前
已完结
[Genetic and clinical characteristics in epilepsy patients with ATP6V1A gene variants]
8天前
已完结
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