Cerebellar atrophy in genetic epileptic encephalopathies: A cohort study and a systematic review-Reference-Cited by-同舟云学术

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Cerebellar atrophy in genetic epileptic encephalopathies: A cohort study and a systematic review

Published:2024-08 Issue: Volume:120 Page:41-48
ISSN:1059-1311
Container-title:Seizure: European Journal of Epilepsy
language:en
Short-container-title:Seizure: European Journal of Epilepsy

Author:

Yang Yao-Lun^ORCID,Lee Hsiu-Fen^ORCID,Chi Ching-Shiang^ORCID,Tsai Chi-Ren^ORCID,Wu Pei-Yu^ORCID,Liu Shu-Ning^ORCID

Publisher

Elsevier BV

Reference28 articles.

1. ILAE classification of the epilepsies: position paper of the ILAE commission for classification and terminology;Scheffer;Epilepsia,2017

2. Developmental and epileptic encephalopathies – therapeutic consequences of genetic testing;Syrbe;Medizinis Genet,2022

3. Inherited developmental and epileptic encephalopathies;Bartolini;Neurol Int,2021

4. The genetic landscape of the epileptic encephalopathies of infancy and childhood;McTague;Lancet Neurol,2016

5. Intrafamilial phenotypic variability in TBC1D24-TLDc homozygous pathogenic variant-related developmental and epileptic encephalopathy;Lee;Clin Neurol Neurosurg,2022

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