Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes (Q57905554)

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19 January 2020

title

Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes (English)

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19 January 2020

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19 January 2020

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19 January 2020

Lynette G Sadleir

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19 January 2020

Bronwyn E Grinton

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19 January 2020

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author name string

Meng-Han Tsai

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19 January 2020

Danya F Vears

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19 January 2020

Leasha M Lillywhite

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Patrick W Carney

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19 January 2020

A Simon Harvey

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publication date

5 January 2012

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19 January 2020

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volume

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issue

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page(s)

319-324

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Benign epilepsy of childhood with Rolandic spikes. A clinical, electroencephalographic, and telencephalographic study

19 January 2020

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Some genetic aspects of rolandic epilepsy: waking and sleep EEGs in siblings

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Speech and oromotor deficits of epileptic origin in benign partial epilepsy of childhood with rolandic spikes (BPERS). Relationship to the acquired aphasia-epilepsy syndrome

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Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2.

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Benign epilepsy of childhood with centrotemporal EEG foci: a genetic study

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Landau-Kleffner syndrome: a clinical and EEG study of five cases

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Increased frequency of rolandic spikes in ADHD children

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Benign childhood epilepsy with centrotemporal spikes: clinical characteristics and identification of patients at risk for multiple seizures

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An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder

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Benign focal epilepsy of childhood. A follow-up study of 100 recovered patients

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Neuropsychological and functional MRI studies provide converging evidence of anterior language dysfunction in BECTS.

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Sylvian Seizures and Midtemporal Spike Foci in Children

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21 January 2018

Identifiers

DOI

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19 January 2020

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