Cargando…
Shared functional network abnormality in patients with temporal lobe epilepsy and their siblings
AIM: Temporal lobe epilepsy is a neurological network disease in which genetics played a greater role than previously appreciated. This study aimed to explore shared functional network abnormalities in patients with sporadic temporal lobe epilepsy and their unaffected siblings. METHODS: Fifty‐eight...
Autores principales: | Wang, Kangrun, Xie, Fangfang, Liu, Chaorong, Wang, Ge, Zhang, Min, He, Jialinzi, Tan, Langzi, Tang, Haiyun, Chen, Fenghua, Xiao, Bo, Song, Yanmin, Long, Lili |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018100/ https://www.ncbi.nlm.nih.gov/pubmed/36647843 http://dx.doi.org/10.1111/cns.14087 |
Ejemplares similares
-
Impaired Cognitive Abilities in Siblings of Patients with Temporal Lobe Epilepsy
por: Tan, Langzi, et al.
Publicado: (2020) -
Cerebellar functional disruption and compensation in mesial temporal lobe epilepsy
por: Peng, Yiqian, et al.
Publicado: (2023) -
Novel PRRT2 gene variants identified in paroxysmal kinesigenic dyskinesia and benign familial infantile epilepsy in Chinese families
por: He, Jialinzi, et al.
Publicado: (2021) -
Structural and functional changes of the cerebellum in temporal lobe epilepsy
por: Wang, Ge, et al.
Publicado: (2023) -
Structural–functional coupling abnormalities in temporal lobe epilepsy
por: Huang, Xiaoting, et al.
Publicado: (2023)