A patient with early myoclonic encephalopathy (EME) with a de novo KCNQ2 mutation
Keywords: KCNQ2; EME; Hypsarrhythmia; Ohtahara syndrome; Burst-suppression;
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Transcriptome of the Wistar audiogenic rat (WAR) strain following audiogenic seizures
Keywords: 5-HT; Serotonin; Acsm3; Acyl-CoA synthetase medium-chain family member 3; Acsm5; Acyl-CoA synthetase medium-chain family member 5; aGPCR; G protein-coupled adhesion receptors; ANOVA; analysis of variance; AS; audiogenic seizure; BH4; tetrahidropteridina;
A KCNQ2 E515D mutation associated with benign familial neonatal seizures and continuous spike and waves during slow-wave sleep syndrome in Taiwan
Keywords: benign familial neonatal seizures; continuous spikes and waves during slow-wave sleep; E515D mutation; KCNQ2;
Research ReportFunctional analysis of potassium channels in Kv7.2 G271V mutant causing early onset familial epilepsy
Keywords: KCNQ2; Kv7.2; Epilepsy; Patch-clamp electrophysiology; Voltage-gated potassium channel;
Discovery of (S,E)-3-(2-fluorophenyl)-N-(1-(3-(pyridin-3-yloxy)phenyl)ethyl)-acrylamide as a potent and efficacious KCNQ2 (Kv7.2) opener for the treatment of neuropathic pain
Keywords: KCNQ2; Kv7.2; Neuropathic pain; Diabetic neuropathy; Acrylamide
Contiguous deletion of KCNQ2 and CHRNA4 may cause a different disorder from benign familial neonatal seizures
Keywords: Benign familial neonatal seizures; KCNQ2; CHRNA4; 20q13.33 deletion
In Silico Cardiac Risk Assessment in Patients With Long QT Syndrome : Type 1: Clinical Predictability of Cardiac Models
Keywords: IKs; KCNQ1; KCNQ2; LQT; QTACA, aborted cardiac arrest; AP, action potential; ECG, electrocardiography; FGM, Flaim-Giles-McCulloch; IKs, rectifier potassium current; LQT1, long QT syndrome type 1; LQTS, long QT syndrome; Q4, upper quartile; QTc, QT interva
Sodium and potassium channel dysfunctions in rare and common idiopathic epilepsy syndromes
Keywords: SCN1A; KCNQ2; KCNQ3; Benign epilepsy of childhood with centrotemporal spikes; Idiopathic epilepsy; Epilepsy genetics
Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions
Keywords: Benign Familial Neonatal Convulsions; BFNC; KCNQ2; Kv7.2; Loss-of-function
Neutralization of a unique, negatively-charged residue in the voltage sensor of KV7.2 subunits in a sporadic case of benign familial neonatal seizures
Keywords: Benign familial neonatal seizures; Potassium channels; Kv7 subunits; Channel gating; Neuronal excitability; Voltage-sensing; Epilepsy; KCNQ2; KCNQ3;
Chronic electroconvulsive stimulation but not chronic restraint stress modulates mRNA expression of voltage-dependent potassium channels Kv7.2 and Kv11.1 in the rat piriform cortex
Keywords: Amy; Amygdala; CA1; CA1 pyramidal cells of hippocampus; CA3; CA3 pyramidal cells of hippocampus; DG; Dentate gyrus; ECT; Electroconvulsive therapy; ECS; Electroconvulsive stimulation; GrCb/Pk; Granule/Purkinje cell layers of the cerebellum; Kv; Voltage-de
Neonatal seizures with tonic clonic sequences and poor developmental outcome
Keywords: Newborn; Electro-encephalography; Developmental disabilities; Epilepsy; Vitamin B6; KCNQ2; Benign familial neonatal convulsions;