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11th European Congress on Epileptology – Stockholm, Sweden – 29th June 3 July 2014

National Registry of Dravet’s Syndrome and other Syndromes correlated with genes SCN1A and PCDH19. – Dalla Bernardina B, Brambilla I, Bianchi F, Paoli D,  Pierini A, Lipucci M   Visualizza abstract e poster  
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Epilessia. Il Lancet Neurology dedica un ritratto in prima pagina a Renzo Guerrini

“Pioniere degli studi di genetica dell’epilessia e di malformazioni della corteccia cerebrale”, Guerrini (Università di Firenze) è “un’autorità” nell’ambito delle neuroscienze e della neuropsichiatria infantile. Sul L

Development and Epilepsy – Strategies for Innovative Research to improve diagnosis, prevention and treatment in children with difficult to treat Epilepsy

Coordinator: Renzo GUERRINI Project Number: 602531 EC contribution: € 11,995,646.00 Project website: under construction DESIRE will focus on epileptogenic developmental disorders EDD, i.e. early onset epilepsies whose origin is closely related to d
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Eurordis Summer School for patient advocates in clinical trials and drug development

02-04 giugno 2014 Barcellona, Spagna http://www.eurordis.org/it/content/eurordis-summer-school-patient-advocates

ECRD 2014 : The European Conference on Rare Diseases & Orphan Products

08-10 maggio 2014 May 2014 Andel’s Hotel, Berlin, Germany http://www.rare-diseases.eu

2nd International Workshop “Rare Disease and Orphan Drug Registries”

Nell’ambito del progetto europeo EPIRARE (European Platform for Rare Disease Registries), co-finanziato dalla Commissione europea e coordinato dal Centro Nazionale Malattie Rare, viene organizzato il II International Workshop “Rare Disease and Or
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