Baomin Li
8PUBLICATIONS
6CO-AUTHORS
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Publications (8)
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|Mar 21, 2025
A rare de novo mutation, m.1630A>G, in the mitochondrial tRNAVal (MT-TV) gene in a child with epilepsy: case report and review of the literature.Qiong Wang, Yan Chen, Jun Li
|May 27, 2024
Attention-deficit/hyperactivity disorder in children with epilepsy: A systematic review and meta-analysis of prevalence and risk factors.Zimeng He, Xiaofan Yang, Yumei Li
|Apr 29, 2021
De novo frameshift variants of HNRNPU in patients with early infantile epileptic encephalopathy: Two case reports and literature review.Zhenfeng Song, Ying Zhang, Chengqing Yang
|Jan 29, 2021
A novel Xp11.22-22.33 deletion suggesting a possible mechanism of congenital cervical spinal muscular atrophy.Jingwei Liu, Kelai Wang, Baomin Li
|Oct 31, 2020
Continuous epileptic negative myoclonus as the first seizure type in atypical benign epilepsy with centrotemporal spikes.Li Yang, Quanping Su, Na Xu
|Apr 03, 2020
Novel and de novo point and large microdeletion mutation in PRRT2-related epilepsy.Li Yang, Cuiping You, Shiyan Qiu
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