Lv1
30 积分 2025-07-07 加入
Clinical, metabolic, and genetic characteristics of 42 children with mitochondrial short-chain enoyl-CoA hydratase 1 deficiency in China
1个月前
已完结
Phenotypes and genotypes of mitochondrial diseases with mtDNA variations in Chinese children: A multi-center study
1个月前
已完结
Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial
7个月前
已完结
Rates and predictors of seizure outcome after corpus callosotomy for drug-resistant epilepsy: a meta-analysis
7个月前
已关闭
CELSR1 variants are associated with partial epilepsy of childhood
8个月前
已完结
Molecular and Synaptic Bases of CDKL5 Disorder
9个月前
已完结
5-mC DNA methylation in neurodevelopment: from molecular mechanisms to therapeutic implications
9个月前
已完结
Research progress on the pathogenesis of CDKL5 pathogenic variants and related encephalopathy
9个月前
已完结
CELSR1 variants are associated with partial epilepsy of childhood
9个月前
已完结
Research progress on the pathogenesis of CDKL5 pathogenic variants and related encephalopathy
9个月前
已完结
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