The Correlation of ELP4-PAX6 With Rolandic Spike Sources in Idiopathic Rolandic Epilepsy Syndromes

Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy

(2018) Dheeraj R. Bobbili et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Progress in unraveling the genetic etiology of rolandic epilepsy

(2017) Weixi Xiong et al.   SEIZURE-EUROPEAN JOURNAL OF EPILEPSY

Averaged EEG spike dipole analysis may predict atypical outcome in Benign Childhood Epilepsy with Centrotemporal Spikes (BCECTS)

(2016) Hunmin Kim et al.   BRAIN & DEVELOPMENT

A microRNA-328 binding site inPAX6is associated with centrotemporal spikes of rolandic epilepsy

(2016) Naim Panjwani et al.   Annals of Clinical and Translational Neurology

Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes

(2015) Eva M. Reinthaler et al.   ANNALS OF NEUROLOGY

Cognition and brain development in children with benign epilepsy with centrotemporal spikes

(2015) Camille Garcia-Ramos et al.   EPILEPSIA

To do or not to do? Magnetoencephalography in the presurgical evaluation of epilepsy

(2015) Cormac A. O'Donovan   EPILEPSY & BEHAVIOR

DEPDC5mutations in genetic focal epilepsies of childhood

(2014) Dennis Lal et al.   ANNALS OF NEUROLOGY

Analysis ofELP4,SRPX2, and interacting genes in typical and atypical rolandic epilepsy

(2014) Eva M. Reinthaler et al.   EPILEPSIA

Association of brain-derived neurotrophic factor (BDNF) and elongator protein complex 4 (ELP4) polymorphisms with benign epilepsy with centrotemporal spikes in a Greek population

(2014) Anastasia Gkampeta et al.   EPILEPSY RESEARCH

16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

(2014) Eva M. Reinthaler et al.   HUMAN MOLECULAR GENETICS

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

(2013) Johannes R Lemke et al.   NATURE GENETICS

GRIN2A mutations cause epilepsy-aphasia spectrum disorders

(2013) Gemma L Carvill et al.   NATURE GENETICS

RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy

(2013) Dennis Lal et al.   PLoS One

Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes

(2012) Danya F. Vears et al.   EPILEPSIA

Emerging genetic influences in benign epilepsy with centro-temporal spikes – BECTS

(2012) Anastasia Gkampeta et al.   EPILEPSY RESEARCH

A review of the relationships between Landau–Kleffner syndrome, electrical status epilepticus during sleep, and continuous spike–waves during sleep

(2011) John R. Hughes   EPILEPSY & BEHAVIOR

Somatotopic distribution of peri-rolandic spikes may predict prognosis in pediatric-onset epilepsy with sensorimotor seizures

(2010) Yosuke Kakisaka et al.   CLINICAL NEUROPHYSIOLOGY

Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009

(2010) Anne T. Berg et al.   EPILEPSIA

Pleiotropic effects of the 11p13 locus on developmental verbal dyspraxia and EEG centrotemporal sharp waves

(2010) D. K. Pal et al.   GENES BRAIN AND BEHAVIOR

Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4)

(2009) Lisa J Strug et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes

(2008) B. A. Neubauer et al.   NEUROLOGY