(Q33861974)

29 July 2017

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title

Neuroimaging and neuropathology of Dravet syndrome. (English)

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29 July 2017

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1

Renzo Guerrini

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29 July 2017

Pasquale Striano

2

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29 July 2017

Claudia Catarino

series ordinal

3

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29 July 2017

Sanjay M Sisodiya

series ordinal

4

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29 July 2017

publication date

1 April 2011

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29 July 2017

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29 July 2017

volume

52 Suppl 2

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29 July 2017

page(s)

30-34

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A long-term follow-up study of Dravet syndrome up to adulthood.

29 July 2017

cites work

1 reference

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21 January 2018

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Severe infant myoclonic epilepsy (author's transl)

21 January 2018

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Focal abnormalities detected by 18FDG PET in epileptic encephalopathies

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02998.X

Polymicrogyria and epilepsy

21 January 2018

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Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN1A gene

21 January 2018

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21 January 2018

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21 January 2018

1 reference

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A case of SUDEP in a patient with Dravet syndrome with SCN1A mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02998.X

SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis.

21 January 2018

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The genetics of Dravet syndrome.

21 January 2018

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Rasmussen encephalitis associated with SCN 1 A mutation.

21 January 2018

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Clinical and neuropathologic findings in a case of severe myoclonic epilepsy of infancy

21 January 2018

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Hemiconvulsion-hemiplegia syndrome in a patient with severe myoclonic epilepsy in infancy

21 January 2018

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Hippocampal sclerosis in severe myoclonic epilepsy in infancy: a retrospective MRI study.

21 January 2018

1 reference

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Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations.

21 January 2018

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Four generations of epilepsy caused by an inherited microdeletion of the SCN1A gene.

21 January 2018

1 reference

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10.1111/J.1528-1167.2011.02998.X

21 January 2018

Identifiers

DOI

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29 July 2017

1 reference