Lv4
480 积分 2024-02-26 加入
Exome sequencing reveals genetic heterogeneity and clinically actionable findings in children with cerebral palsy
1个月前
已完结
Unravelling the genetic complexity of drug-resistant epilepsy: a critical narrative review
2个月前
已完结
The interaction of UBR4, LRP1, and OPHN1 in refractory epilepsy: Drosophila model to investigate the oligogenic effect on epilepsy
2个月前
已完结
Expansion of the Epilepsy Genotype-Phenotype Spectrum: Genetic and Clinical Characterization of 288 Children with Epilepsy in China
2个月前
已完结
Loss of Function SPTAN1 Variants Result in Ataxia and Intellectual Disability
2个月前
已完结
Harnessing FDA-approved dipyridamole to inhibit NLRP3 inflammasome and improve outcomes of acute lung injury in sepsis
2个月前
已完结
Antiviral treatment for influenza in Japan
3个月前
已关闭
Summary of WHO clinical practice guidelines for influenza
3个月前
已完结
Mild phenotype of a de novo partial trisomy 13q22.2-qter: case report and review of the literature
4个月前
已关闭
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