Targeted treatment of migrating partial seizures of infancy with quinidine

KCNT1gain of function in 2 epilepsy phenotypes is reversed by quinidine

(2014) Carol J. Milligan et al.   ANNALS OF NEUROLOGY

SLC25A22is a novel gene for migrating partial seizures in infancy

(2013) Annapurna Poduri et al.   ANNALS OF NEUROLOGY

Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum

(2013) Amy McTague et al.   BRAIN

Novel Compound Heterozygous Mutations inTBC1D24Cause Familial Malignant Migrating Partial Seizures of Infancy

(2013) Mathieu Milh et al.   HUMAN MUTATION

Novel de novo SCN2A Mutation in a Child With Migrating Focal Seizures of Infancy

(2013) Radhika Dhamija et al.   PEDIATRIC NEUROLOGY

Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy

(2012) Annapurna Poduri et al.   EPILEPSIA

De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy

(2012) Giulia Barcia et al.   NATURE GENETICS

Novel SCN1A Mutation in a Proband With Malignant Migrating Partial Seizures of Infancy

(2011) Emily R. Freilich et al.   ARCHIVES OF NEUROLOGY

Fragile X mental retardation protein controls gating of the sodium-activated potassium channel Slack

(2010) Maile R Brown et al.   NATURE NEUROSCIENCE

Malignant migrating partial seizures in infancy: An epilepsy syndrome of unknown etiology

(2009) Giangennaro Coppola   EPILEPSIA

Amino-termini isoforms of the Slack K+channel, regulated by alternative promoters, differentially modulate rhythmic firing and adaptation

(2008) Maile R. Brown et al.   JOURNAL OF PHYSIOLOGY-LONDON