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Epilepsy, Rolandic

Known as: epilepsy roland, Epilepsy, Sylvian, Epilepsies, Rolandic 
An autosomal dominant inherited partial epilepsy syndrome with onset between age 3 and 13 years. Seizures are characterized by PARESTHESIA and tonic… 
National Institutes of Health

Papers overview

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Highly Cited
2007
Highly Cited
2007
Summary:  Methods: A multicenter, randomized, open‐label, observer‐blinded, parallel‐group clinical trial was conducted. TPM was… 
Review
2007
Review
2007
Preface. 1.1 From Gene to Product: The Advantage of Integrative Biotechnology (Frank-Ranier Schmidt). 1.2 Sequencing the Human… 
2006
2006
Summary:  Purpose: To report two families combining benign childhood epilepsy with centrotemporal spikes (BCECS) and cryptogenic… 
2004
2004
PURPOSE Some children with rolandic epilepsy have associated neuropsychiatric deficits resembling symptoms of attention deficit… 
2002
2002
I. Otologic Surgery Tympanostomy Tubes and Related Procedures- Charles D. Bluestone Approaches to the Middle Ear and Mastoid… 
Review
2001
Review
2001
This paper reviews the main studies which have evaluated precisely cognitive functions in rolandic epilepsy. There are very few… 
2001
2001
BACKGROUND Long-term outcome of rolandic epilepsy (RE) is associated with a diversity of neuropsychological deficits in childhood… 
Review
2001
Review
2001
Benign rolandic epilepsy is the most common epilepsy of childhood. Regarding seizure control typical and atypical rolandic… 
Highly Cited
1990
Highly Cited
1990
Summary: Epileptic activity was recorded electroen‐cephalographically in at least one sibling in 22 (51.16%) of 43 patients with…