EDITORIAL
Published on 21 Sep 2022
Editorial: Ion channels and transporters in epilepsy: From genes and mechanisms to disease-targeted therapies
doi 10.3389/fnmol.2022.1011843
- 2,191 views
- Frontiers in Molecular Neuroscience
- Brain Disease Mechanisms
- Research Topics
- Ion Channels and Transporters in Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies
Ion Channels and Transporters in Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies
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Articles
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Novel HCN1 Mutations Associated With Epilepsy and Impacts on Neuronal Excitability
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ORIGINAL RESEARCH
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- 3 citations
ORIGINAL RESEARCH
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Functional Characterization of CLCN4 Variants Associated With X-Linked Intellectual Disability and Epilepsy
doi 10.3389/fnmol.2022.872407
- 2,552 views
- 13 citations
ORIGINAL RESEARCH
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SCN1A-Related Epilepsy: Novel Mutations and Rare Phenotypes
doi 10.3389/fnmol.2022.826183
- 3,602 views
- 3 citations
SYSTEMATIC REVIEW
Published on 19 May 2022
The Contribution of HCN Channelopathies in Different Epileptic Syndromes, Mechanisms, Modulators, and Potential Treatment Targets: A Systematic Review
doi 10.3389/fnmol.2022.807202
- 4,787 views
- 24 citations
ORIGINAL RESEARCH
Published on 28 Apr 2022
Phenotypic and Genotypic Characteristics of SCN1A Associated Seizure Diseases
doi 10.3389/fnmol.2022.821012
- 4,737 views
- 13 citations
ORIGINAL RESEARCH
Published on 26 Apr 2022
Clinical Study of 30 Novel KCNQ2 Variants/Deletions in KCNQ2-Related Disorders
doi 10.3389/fnmol.2022.809810
- 2,822 views
- 5 citations
ORIGINAL RESEARCH
Published on 30 Mar 2022
SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis
doi 10.3389/fnmol.2022.809951
- 17,784 views
- 21 citations
ORIGINAL RESEARCH
Published on 16 Mar 2022
Functional Investigation of a Neuronal Microcircuit in the CA1 Area of the Hippocampus Reveals Synaptic Dysfunction in Dravet Syndrome Mice
doi 10.3389/fnmol.2022.823640
- 3,494 views
- 13 citations
ORIGINAL RESEARCH
Published on 14 Mar 2022
Phenotypic Spectrum and Prognosis of Epilepsy Patients With GABRG2 Variants
doi 10.3389/fnmol.2022.809163
- 6,248 views
- 6 citations
Published in
Frontiers in Molecular Neuroscience
- Brain Disease Mechanisms
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