EDITORIAL
Published on 25 Sep 2020
Editorial: Epilepsy and Neurodevelopmental Diseases
doi 10.3389/fncel.2020.00255
- 1,663 views
- Frontiers in Cellular Neuroscience
- Cellular Neuropathology
- Research Topics
- Epilepsy and Neurodevelopmental Diseases
Epilepsy and Neurodevelopmental Diseases
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Articles
ORIGINAL RESEARCH
Published on 08 May 2020
Multimodal Analysis of STRADA Function in Brain Development
doi 10.3389/fncel.2020.00122
- 3,483 views
- 13 citations
ORIGINAL RESEARCH
Published on 20 Mar 2020
Paroxysmal Discharges in Tissue Slices From Pediatric Epilepsy Surgery Patients: Critical Role of GABAB Receptors in the Generation of Ictal Activity
doi 10.3389/fncel.2020.00054
- 2,913 views
- 9 citations
ORIGINAL RESEARCH
Published on 17 Mar 2020
Granule Cell Dispersion in Human Temporal Lobe Epilepsy: Proteomics Investigation of Neurodevelopmental Migratory Pathways
doi 10.3389/fncel.2020.00053
- 5,373 views
- 20 citations
MINI REVIEW
Published on 13 Mar 2020
Emerging Role of the Autophagy/Lysosomal Degradative Pathway in Neurodevelopmental Disorders With Epilepsy
doi 10.3389/fncel.2020.00039
- 5,711 views
- 31 citations
MINI REVIEW
Published on 13 Feb 2020
A Reappraisal of GAT-1 Localization in Neocortex
doi 10.3389/fncel.2020.00009
- 3,263 views
- 32 citations
ORIGINAL RESEARCH
Published on 24 Jan 2020
The Epilepsy of Infancy With Migrating Focal Seizures: Identification of de novo Mutations of the KCNT2 Gene That Exert Inhibitory Effects on the Corresponding Heteromeric KNa1.1/KNa1.2 Potassium Channel
doi 10.3389/fncel.2020.00001
- 5,038 views
- 29 citations
MINI REVIEW
Published on 14 Jan 2020
Transcriptional Regulation of Channelopathies in Genetic and Acquired Epilepsies
doi 10.3389/fncel.2019.00587
- 4,377 views
- 16 citations
MINI REVIEW
Published on 13 Dec 2019
Functional Genomics of Epilepsy and Associated Neurodevelopmental Disorders Using Simple Animal Models: From Genes, Molecules to Brain Networks
doi 10.3389/fncel.2019.00556
- 4,559 views
- 18 citations
MINI REVIEW
Published on 15 Nov 2019
Identification of KCC2 Mutations in Human Epilepsy Suggests Strategies for Therapeutic Transporter Modulation
doi 10.3389/fncel.2019.00515
- 5,669 views
- 33 citations
BRIEF RESEARCH REPORT
Published on 26 Sep 2019
Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in ATP1A3
doi 10.3389/fncel.2019.00425
- 4,397 views
- 20 citations
Published in
Frontiers in Cellular Neuroscience
- Cellular Neuropathology
- Non-Neuronal Cells
- Cellular Neurophysiology
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