Co-occurring malformations of cortical development andSCN1Agene mutations

Author:

Barba Carmen1,Parrini Elena1,Coras Roland2,Galuppi Anna1,Craiu Dana3,Kluger Gerhard45,Parmeggiani Antonia6,Pieper Tom4,Schmitt-Mechelke Thomas7,Striano Pasquale8,Giordano Flavio9,Blumcke Ingmar2,Guerrini Renzo110

Affiliation:

1. Pediatric Neurology Unit and Laboratories; Children's Hospital Meyer-University of Florence; Florence Italy

2. Department of Neuropathology; University Hospital; Erlangen Germany

3. Pediatric Neurology Clinic; Al Obregia Hospital; Bucharest Romania

4. Department of Neuropediatrics; Epilepsy Center; Vogtareuth Germany

5. Paracelsus Medical University Salzburg; Salzburg Austria

6. Child Neurology and Psychiatry Unit; Department of Medical and Surgical Sciences; Policlinico S. Orsola-Malpighi; University of Bologna; Bologna Italy

7. Department of Neuropediatrics; Pediatric Hospital; Lucerne Switzerland

8. Pediatric Neurology and Muscular Diseases Unit; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health; G. Gaslini Institute; University of Genoa; Genoa Italy

9. Pediatric Neurosurgery Unit; Children's Hospital Meyer-University of Florence; Florence Italy

10. IRCCS Stella Maris; Calambrone; Pisa Italy

Funder

European Union Seventh Framework Programme

DESIRE

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference45 articles.

1. Severe myoclonic epilepsy in infancy: Dravet syndrome;Dravet;Adv Neurol,2005

2. SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis;Marini;Epilepsia,2009

3. The core Dravet syndrome phenotype;Dravet;Epilepsia,2011

4. Dravet syndrome: the main issues;Guerrini;Eur J Paediatr Neurol,2012

5. Hippocampal sclerosis in severe myoclonic epilepsy in infancy: a retrospective MRI study;Siegler;Epilepsia,2005

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