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… (More)
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
Idiopathic focal epilepsy (IFE) with rolandic spikes is the most common childhood epilepsy, comprising a phenotypic spectrum from… (More)
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Highly Cited
2013
Highly Cited
2013
Epileptic encephalopathies are severe brain disorders with the epileptic component contributing to the worsening of cognitive and… (More)
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Highly Cited
2009
Highly Cited
2009
Rolandic epilepsy (RE) is the most common human epilepsy, affecting children between 3 and 12 years of age, boys more often than… (More)
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Review
2008
Review
2008
A big advance in epileptology has been the recognition of syndromes with distinct aetiology, clinical and EEG features, treatment… (More)
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Highly Cited
2007
Highly Cited
2007
PURPOSE Associations between rolandic epilepsy (RE) with reading disability (RD) and speech sound disorder (SSD) have not been… (More)
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Highly Cited
2006
Highly Cited
2006
The present study used pleasant and unpleasant music to evoke emotion and functional magnetic resonance imaging (fMRI) to… (More)
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Highly Cited
2005
Highly Cited
2005
PURPOSE Benign rolandic epilepsy (BRE) has an excellent prognosis for seizures, but recent research has raised concerns using… (More)
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Highly Cited
2002
Highly Cited
2002
Although fatigue is a common and troublesome symptom of multiple sclerosis (MS), its pathogenesis is poorly understood. In this… (More)
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Highly Cited
2001
Highly Cited
2001
BACKGROUND Although so-called "benign" epilepsy with centrotemporal spikes (BECTS) always has an excellent prognosis with regard… (More)
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Highly Cited
1998
Highly Cited
1998
OBJECTIVE To localize a gene predisposing to benign epilepsy of childhood with centrotemporal spikes (BECTS). BACKGROUND BECTS… (More)
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