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Berten Ceulemans, Kern Olofson, Katrijn Arts, Robin Cloarec, Elisabeth Cats, Joost Nicolai, Charissa Millevert, Matthias De Wachter, Cathrine Elisabeth Gjerulfsen, Magdalena Krygier, Steffen Syrbe, Allan Bayat, Stephane Auvin, Rikke S Møller, Gerhard Kluger, Sarah Weckhuysen, Mathieu Milh, Katrien Jansen, Robert Smigiel

Epilepsia 2025;66(5):1628-1640

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KCNQ2/KCNQ3 K+ channels and the molecular pathogenesis of epilepsy: implications for therapy.

M A Rogawski

Trends in neurosciences 2000;23(9):393-8

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Neurotransmitter Pathway Genes in Cognitive Decline During Aging: Evidence for GNG4 and KCNQ2 Genes.

Daniel S Evans, Jennifer S Yokoyama, Kristine Yaffe, Steven R Cummings, Yongmei Liu, Luke W Bonham

American journal of Alzheimer's disease and other dementias 2019;33(3):153-165

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Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort.

Yuehua Zhang, Liping Wei, Xiru Wu, Ye Wu, Xiaoyan Liu, Zhixian Yang, Aijie Liu, Jing Zhang, Xiaoling Yang, Qi Zeng

Journal of human genetics 2018;63(1):9-18

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Capturing seizures in clinical trials of antiseizure medications for -DEE.

Simon N Pimstone, Ernesto Aycardi, Celene Grayson, Jacqueline A French, Noam N Butterfield, Dennis J Dlugos, Cynthia L Harden, John J Millichap

Epilepsia open 2021;6(1):38-44

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Pathogenic convergence of CNVs in genes functionally associated to a severe neuromotor developmental delay syndrome.

Pedro A Lazo, Carmen Fons, Paulino Gómez-Puertas, Íñigo Marcos-Alcalde, Luis A Corchete, Juan L García-Hernández

Human genomics 2022;15(1):11

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Results for ""KCNQ2 Potassium Channel""[mesh_terms]

Antiepileptic therapy approaches in KCNQ2 related epilepsy: A systematic review.

Pyridoxine-responsive KCNQ2 epileptic encephalopathy: Additional cases and literature review.

Video/EEG findings in a KCNQ2 epileptic encephalopathy: a case report and revision of literature data.

Why we urgently need improved seizure and epilepsy therapies for children and neonates.

KCNQ2-Related Epilepsy: Genotype-Phenotype Relationship with Tailored Antiseizure Medication (ASM)-A Systematic Review.

Novel Dominant KCNQ2 Exon 7 Partial In-Frame Duplication in a Complex Epileptic and Neurodevelopmental Delay Syndrome.

Cerebellar Hypoplasia and Treatment Course of a Two-Month-Old Infant With KCNQ2 Epileptic Encephalopathy Due to a De Novo Variant and Review of the Literature.

Genetics of neonatal-onset epilepsies.

Potassium channels and epilepsy.

Amitriptyline use in individuals with KCNQ2/3 gain-of-function variants: A retrospective cohort study.

KCNQ2/KCNQ3 K+ channels and the molecular pathogenesis of epilepsy: implications for therapy.

Neurotransmitter Pathway Genes in Cognitive Decline During Aging: Evidence for GNG4 and KCNQ2 Genes.

Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort.

Capturing seizures in clinical trials of antiseizure medications for -DEE.

Pathogenic convergence of CNVs in genes functionally associated to a severe neuromotor developmental delay syndrome.

Results for
""KCNQ2 Potassium Channel""[mesh_terms]