(Q36319387)

13 August 2017

1 reference

title

Syndromes of idiopathic generalized epilepsies not recognized by the International League Against Epilepsy (English)

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13 August 2017

author name string

Chrysostomos P Panayiotopoulos

series ordinal

1

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13 August 2017

publication date

1 January 2005

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13 August 2017

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13 August 2017

volume

46 Suppl 9

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13 August 2017

page(s)

57-66

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A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: report of the ILAE Task Force on Classification and Terminology

13 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

Absence epilepsy with onset before age three years: a heterogeneous and often severe condition

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

Perioral myoclonia with absences? A case report with EEG and voltage mapping analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

Typical absence status in adults: diagnostic and syndromic considerations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

Recurrent absence status epilepticus: clinical and EEG characteristics

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

Distinct behavioral and EEG topographic correlates of loss of consciousness in absences.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

Idiopathic generalised epilepsy of adult onset: clinical syndromes and genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

Eyelid myoclonia with absences in adults: a clinical and video-EEG study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

Eyelid myoclonia with absences: phenomenology in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

Mapping of a locus for a familial autosomal recessive idiopathic myoclonic epilepsy of infancy to chromosome 16p13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

Familial infantile myoclonic epilepsy: clinical features in a large kindred with autosomal recessive inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

Cortical tremor: a variant of cortical reflex myoclonus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

Familial cortical myoclonic tremor as a unique form of cortical reflex myoclonus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

Positional candidate approach for the gene responsible for benign adult familial myoclonic epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

A novel giant gene CSMD3 encoding a protein with CUB and sushi multiple domains: a candidate gene for benign adult familial myoclonic epilepsy on human chromosome 8q23.3-q24.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2005.00314.X

10.1111/J.1528-1167.2005.00314.X

21 January 2018

Identifiers

DOI

1 reference

13 August 2017

1 reference