Benign epilepsy in children. (Q37865802)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21497276 AND SRC:MED&resulttype=core&format=json

28 January 2020

review article

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title

Benign epilepsy in children (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21497276 AND SRC:MED&resulttype=core&format=json

28 January 2020

2

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28 January 2020

author name string

Sook-Cheng Chan

series ordinal

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21497276 AND SRC:MED&resulttype=core&format=json

28 January 2020

publication date

1 March 2011

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Journal of the Formosan Medical Association

28 January 2020

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21497276 AND SRC:MED&resulttype=core&format=json

28 January 2020

volume

110

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21497276 AND SRC:MED&resulttype=core&format=json

28 January 2020

issue

3

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28 January 2020

page(s)

134-144

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Treatment of benign epilepsy syndromes throughout life

28 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Benign familial and non-familial infantile seizures (Fukuyama-Watanabe-Vigevano syndrome): a study of 14 cases from Saudi Arabia.

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Benign infantile seizures: a prospective study

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Clinical and genetic study on a new Chinese family with benign familial infantile seizures

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

A novel SCN2A mutation in family with benign familial infantile seizures

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

A BFIS-like syndrome with late onset and febrile seizures: suggestive linkage to chromosome 16p11.2-16q12.1.

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

SCN2A Mutations and Benign Familial Neonatal-Infantile Seizures: The Phenotypic Spectrum

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Idiopathic generalized epilepsy with absences: syndrome classification.

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Idiopathic generalized epilepsy (IGE) syndromes in development: IGE with absences of early childhood, IGE with phantom absences, and perioral myoclonia with absences

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Childhood absence epilepsy: behavioral, cognitive, and linguistic comorbidities

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Language in pediatric epilepsy

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Brain imaging in idiopathic generalized epilepsies

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Frontal and temporal volumes in Childhood Absence Epilepsy

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Simultaneous EEG-fMRI in drug-naive children with newly diagnosed absence epilepsy

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Use of a new antiepileptic drug or an old one as first drug for treatment of absence epilepsy

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Lamotrigine versus valproic acid as first-line monotherapy in newly diagnosed typical absence seizures: an open-label, randomized, parallel-group study.

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Levetiracetam for the treatment of idiopathic generalized epilepsy with myoclonic seizures

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Topiramate monotherapy for childhood absence seizures: an open label pilot study

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

MR spectroscopy shows reduced frontal lobe concentrations of N-acetyl aspartate in patients with juvenile myoclonic epilepsy

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Magnetic resonance spectroscopy reveals an epileptic network in juvenile myoclonic epilepsy

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Frontal cognitive dysfunction in juvenile myoclonic epilepsy

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Voxel-based morphometry in patients with idiopathic generalized epilepsies

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Neuropsychological profile of patients with juvenile myoclonic epilepsy: a controlled study of 50 patients

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Visual working memory in primary generalized epilepsy: an 18FDG-PET study

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Evaluation of cognition, structural, and functional MRI in juvenile myoclonic epilepsy

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Benign childhood focal epilepsies: assessment of established and newly recognized syndromes

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Benign epilepsy with centrotemporal spikes

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Atypical rolandic epilepsy

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Drug treatment of benign focal epilepsies of childhood

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Antiepileptic drug treatment of benign childhood epilepsy with rolandic spikes: is it necessary?

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Predictive factors of seizure frequency and duration of antiepileptic treatment in rolandic epilepsy: a retrospective study

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

The course of benign partial epilepsy of childhood with centrotemporal spikes: a meta-analysis.

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

A pilot study transitioning children onto levetiracetam monotherapy to improve language dysfunction associated with benign rolandic epilepsy

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Analyzing the etiology of benign rolandic epilepsy: a multicenter twin collaboration.

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

SRPX2 mutations in disorders of language cortex and cognition

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

From rolandic epilepsy to continuous spike-and-waves during sleep and Landau-Kleffner syndromes: insights into possible genetic factors

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Intellectual and language findings and their relationship to EEG characteristics in benign childhood epilepsy with centrotemporal spikes

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Attention impairment in rolandic epilepsy: systematic review

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Neuropsychological disorders related to interictal epileptic discharges during sleep in benign epilepsy of childhood with centrotemporal or Rolandic spikes

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Benign partial epilepsy in childhood: selective cognitive deficits are related to the location of focal spikes determined by combined EEG/MEG.

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Language in benign childhood epilepsy with centro-temporal spikes abbreviated form: rolandic epilepsy and language

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Cortical auditory dysfunction in benign rolandic epilepsy

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Report of the ILAE classification core group

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

The birth and evolution of the concept of Panayiotopoulos syndrome

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Changes in Panayiotopoulos syndrome over time

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Panayiotopoulos syndrome: an important electroclinical example of benign childhood system epilepsy

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Benign occipital epilepsies of childhood: clinical features and genetics

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Autonomic status epilepticus in Panayiotopoulos syndrome and other childhood and adult epilepsies: a consensus view

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Panayiotopoulos syndrome: a prospective study of 192 patients

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Panayiotopoulos syndrome: epidemiological and clinical characteristics and outcome

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Clinical analysis of childhood occipital lobe epilepsy in 43 Taiwanese patients

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Ictal asystole: a benign condition?

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Panayiotopoulos syndrome: a benign childhood autonomic epilepsy frequently imitating encephalitis, syncope, migraine, sleep disorder, or gastroenteritis

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

EEG dipole characteristics in Panayiotopoulos syndrome

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Neurobehavioral abnormalities may correlate with increased seizure burden in children with Panayiotopoulos syndrome

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Panayiotopoulos syndrome: a consensus view

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

A new type of epilepsy: benign partial epilepsy of childhood with occipital spike-waves

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Childhood occipital epilepsy of Gastaut: a study of 33 patients

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

Levetiracetam monotherapy for childhood occipital epilepsy of gastaut

1 reference

https://api.crossref.org/works/10.1016/S0929-6646(11)60023-5

7 January 2021

10.1016/S0929-6646(11)60023-5

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21497276 AND SRC:MED&resulttype=core&format=json

28 January 2020

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