Article info
Image of the moment
Periventricular heterotopias with incomplete agenesis of corpus callosum and prolonged focal seizures
- Correspondence to Dr Moshe Herskovitz, Epilepsy Service, Department of Neurology, Rambam Medical Center, 1 Efron St Haifa 31096 Israel; m_herskovitz{at}rambam.health.gov.il
Citation
Periventricular heterotopias with incomplete agenesis of corpus callosum and prolonged focal seizures
Publication history
- First published March 6, 2013.
Online issue publication
April 14, 2016
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions
Other content recommended for you
- Clinical features and long term outcome of epilepsy in periventricular nodular heterotopia. Simple compared with plus forms
- Oculocerebrocutaneous syndrome: the brain malformation defines a core phenotype
- Agenesis of the corpus callosum with interhemispheric cyst: clinical implications and outcome
- Further characterisation of ARX-related disorders in females due to inherited or de novo variants
- ARF1 haploinsufficiency causes periventricular nodular heterotopia with variable clinical expressivity
- CONGENITAL ABNORMALITIES OF THE CENTRAL NERVOUS SYSTEM
- Microcephalic osteodysplastic primordial dwarfism type 1
- Colpocephaly in adults
- Bilateral periventricular nodular heterotopia in France: frequency of mutations in FLNA, phenotypic heterogeneity and spectrum of mutations
- De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities