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Doose syndrome (myoclonic–astatic epilepsy): 40 years of progress

Doose syndrome (myoclonic–astatic epilepsy): 40 years of progress

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_821193268

Doose syndrome (myoclonic–astatic epilepsy): 40 years of progress

About this item

Full title

Doose syndrome (myoclonic–astatic epilepsy): 40 years of progress

Publisher

Oxford, UK: Blackwell Publishing Ltd

Journal title

Developmental medicine and child neurology, 2010-11, Vol.52 (11), p.988-993

Language

English

Formats

Publication information

Publisher

Oxford, UK: Blackwell Publishing Ltd

More information

Scope and Contents

Contents

Doose syndrome, otherwise traditionally known as myoclonic–astatic epilepsy, was first described as a unique epilepsy syndrome by Dr Hermann Doose in 1970. In 1989, the International League Against Epilepsy classified it formally as a symptomatic generalized epilepsy, and 20 years later it was renamed ‘epilepsy with myoclonic–atonic seizures’. In t...

Alternative Titles

Full title

Doose syndrome (myoclonic–astatic epilepsy): 40 years of progress

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_821193268

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_821193268

Other Identifiers

ISSN

0012-1622

E-ISSN

1469-8749

DOI

10.1111/j.1469-8749.2010.03744.x

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