Potassium channels Brief overview and implications in epilepsy

[21] Randomized, multicenter, dose-ranging trial of retigabine for partial-onset seizures [J]. NEUROLOGY, 2007, 68 (15) : 1197 - 1204

[22] Mechanism of action of a sulphonylurea receptor SUR1 mutation (F132L) that causes DEND syndrome [J]. HUMAN MOLECULAR GENETICS, 2007, 16 (16) : 2011 - 2019

[23] Variable K+ channel subunit dysfunction in inherited mutations of KCNA1 [J]. JOURNAL OF PHYSIOLOGY-LONDON, 2002, 538 (01): : 5 - 23

[24] The epilepsy-linked Lgi1 protein assembles into presynaptic Kv1 channels and inhibits inactivation by Kvβ1 [J]. NEURON, 2006, 49 (05) : 697 - 706

[25] Shieh CC, 2000, PHARMACOL REV, V52, P557

[26] A novel mutation causing DEND syndrome -: A treatable channelopathy of pancreas and brain [J]. NEUROLOGY, 2007, 69 (13) : 1342 - 1349

[27] Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization [J]. JOURNAL OF PHYSIOLOGY-LONDON, 2008, 586 (14): : 3405 - 3423

[28] Deletion of the Kv1.1 potassium channel causes epilepsy in mice [J]. NEURON, 1998, 20 (04) : 809 - 819

[29] Clinical spectrum of voltage-gated potassium channel autoimmunity [J]. NEUROLOGY, 2008, 70 (20) : 1883 - 1890

[30] Localization of voltage-gated ion channels in mammalian brain [J]. ANNUAL REVIEW OF PHYSIOLOGY, 2004, 66 : 477 - 519

[21] Randomized, multicenter, dose-ranging trial of retigabine for partial-onset seizures [J]. NEUROLOGY, 2007, 68 (15) : 1197 - 1204

[22] Mechanism of action of a sulphonylurea receptor SUR1 mutation (F132L) that causes DEND syndrome [J]. HUMAN MOLECULAR GENETICS, 2007, 16 (16) : 2011 - 2019

[23] Variable K+ channel subunit dysfunction in inherited mutations of KCNA1 [J]. JOURNAL OF PHYSIOLOGY-LONDON, 2002, 538 (01): : 5 - 23

[24] The epilepsy-linked Lgi1 protein assembles into presynaptic Kv1 channels and inhibits inactivation by Kvβ1 [J]. NEURON, 2006, 49 (05) : 697 - 706

[25] Shieh CC, 2000, PHARMACOL REV, V52, P557

[26] A novel mutation causing DEND syndrome -: A treatable channelopathy of pancreas and brain [J]. NEUROLOGY, 2007, 69 (13) : 1342 - 1349

[27] Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization [J]. JOURNAL OF PHYSIOLOGY-LONDON, 2008, 586 (14): : 3405 - 3423

[28] Deletion of the Kv1.1 potassium channel causes epilepsy in mice [J]. NEURON, 1998, 20 (04) : 809 - 819

[29] Clinical spectrum of voltage-gated potassium channel autoimmunity [J]. NEUROLOGY, 2008, 70 (20) : 1883 - 1890

[30] Localization of voltage-gated ion channels in mammalian brain [J]. ANNUAL REVIEW OF PHYSIOLOGY, 2004, 66 : 477 - 519