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ArticlesPeer ReviewedFull Text
Dravet syndrome history
Author / Creator:DRAVET, CHARLOTTE
Publisher:Oxford, UK: Blackwell Publishing Ltd
Journal title:Developmental medicine and child neurology, 2011-04, Vol.53 (s2), p.1-6
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ArticlesPeer ReviewedFull Text
Different Outcomes of Acute Encephalopathy after Status Epilepticus in Patients with Dravet Syndrome. How to Avoid Them? Comment on De Liso et al. Fatal Status Epilepticus in Dravet Syndrome. Brain Sc...
Author / Creator:Dravet, Charlotte
Publisher:Basel: MDPI AG
Journal title:Brain sciences, 2021-06, Vol.11 (6), p.792
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ArticlesPeer ReviewedFull Text
Dravet Syndrome: Addressing the Needs of Patients and Families: Introduction
Author / Creator:Dravet, Charlotte
Publisher:New York, USA: Cambridge University Press
Journal title:Canadian journal of neurological sciences, 2016-06, Vol.43 (S3), p.S1-S2
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ArticlesPeer ReviewedFull Text
Dravet Syndrome: Addressing the Needs of Patients and Families: Conclusion
Author / Creator:Dravet, Charlotte
Publisher:New York, USA: Cambridge University Press
Journal title:Canadian journal of neurological sciences, 2016-06, Vol.43 (S3), p.S19-S20
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Newsletter articlesFull Text
Unrelated girls share rare disorder
Author / Creator:Boen, Jennifer L
Publisher:Washington: Tribune Content Agency LLC
Journal title:McClatchy - Tribune News Service, 2008, p.1
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Newsletter articlesFull Text
Tot captures the hearts of emergency crews: FIREFIGHTER ANTHONY BALASTER: ?She's like part of the family to every one of us.?
Author / Creator:Tokasz, Jay
Publisher:Washington: Tribune Content Agency LLC
Journal title:McClatchy - Tribune Business News, 2007, p.1
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Newsletter articlesFull Text
Parents' quest aids daughter: They gather, share info about rare disorder
Author / Creator:Boen, Jennifer L
Publisher:Washington: Tribune Content Agency LLC
Journal title:McClatchy - Tribune News Service, 2007, p.1
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Newsletter articlesFull Text
Parents seek aid for tot with rare disease
Author / Creator:Cardine, Sara
Publisher:Washington: Tribune Content Agency LLC
Journal title:McClatchy - Tribune Business News, 2006, p.1
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Newsletter articlesFull Text
Parents' quest aids daughter: They gather, share info about rare disorder
Author / Creator:Boen, Jennifer L
Publisher:Washington: Tribune Content Agency LLC
Journal title:McClatchy - Tribune Business News, 2007, p.1
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Newspaper ArticlesFull Text
Dravet syndrome
Author / Creator:Cuda, Amanda
Publisher:Washington: Tribune Content Agency LLC
Journal title:Knight-Ridder/Tribune Business News, 2006-11-19, p.1
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ArticlesPeer ReviewedFull Text
Prognostic Factors for Childhood and Juvenile Absence Epilepsies
Author / Creator:Bartolomei, Fabrice ; Roger, Joseph ; Bureau, Michelle ; Genton, Pierre ; Dravet, Charlotte ; Viallat, Danielle ; Gastaut, Jean-Louis
Publisher:Basel, Switzerland: Karger
Journal title:European neurology, 1997-01, Vol.37 (3), p.169-175
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ArticlesPeer ReviewedFull Text
Epilepsy and BRAF Mutations: Phenotypes, Natural History and Genotype-Phenotype Correlations
Author / Creator:Battaglia, Domenica I. ; Gambardella, Maria Luigia ; Veltri, Stefania ; Contaldo, Ilaria ; Chillemi, Giovanni ; Veredice, Chiara ; Quintiliani, Michela ; Leoni, Chiara ; Onesimo, Roberta ; Verdolotti, Tommaso ; Radio, Francesca Clementina ; Martinelli, Diego ; Trivisano, Marina ; Specchio, Nicola ; Dravet, Charlotte ; Tartaglia, Marco ; Zampino, Giuseppe
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2021-08, Vol.12 (9), p.1316
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ArticlesPeer ReviewedFull Text
Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome
Author / Creator:Depienne, Christel ; Trouillard, Oriane ; Gourfinkel-An, Isabelle ; Saint-Martin, Cécile ; Bouteiller, Delphine ; Graber, Denis ; Barthez-Carpentier, Marie-Anne ; Gautier, Agnès ; Villeneuve, Nathalie ; Dravet, Charlotte ; Livet, Marie-Odile ; Rivier-Ringenbach, Clothilde ; Adam, Claude ; Dupont, Sophie ; Baulac, Stéphanie ; Héron, Delphine ; Nabbout, Rima ; LeGuern, Eric
Publisher:London: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2010-06, Vol.47 (6), p.404-410
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ArticlesPeer ReviewedFull Text
Parental mosaicism can cause recurrent transmission of SCN1A mutations associated with severe myoclonic epilepsy of infancy
Author / Creator:Depienne, Christel ; Arzimanoglou, Alexis ; Trouillard, Oriane ; Fedirko, Estelle ; Baulac, Stéphanie ; Saint-Martin, Cécile ; Ruberg, Merle ; Dravet, Charlotte ; Nabbout, Rima ; Baulac, Michel ; Gourfinkel-An, Isabelle ; Leguern, Eric
Publisher:Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2006-04, Vol.27 (4), p.389-389
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ArticlesPeer ReviewedFull Text
Treatment of Dravet Syndrome
Author / Creator:Wirrell, Elaine C.
Publisher:New York, USA: Cambridge University Press
Journal title:Canadian journal of neurological sciences, 2016-06, Vol.43 (S3), p.S13-S18
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ArticlesPeer ReviewedFull Text
Dravet Syndrome: Diagnosis and Long-Term Course
Author / Creator:Connolly, Mary B.
Publisher:New York, USA: Cambridge University Press
Journal title:Canadian journal of neurological sciences, 2016-06, Vol.43 (S3), p.S3-S8
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ArticlesPeer ReviewedFull Text
Helping Families Cope with the Severe Stress of Dravet Syndrome
Author / Creator:Camfield, Peter ; Camfield, Carol ; Nolan, Kathleen
Publisher:New York, USA: Cambridge University Press
Journal title:Canadian journal of neurological sciences, 2016-06, Vol.43 (S3), p.S9-S12
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ArticlesPeer ReviewedFull Text
Parental mosaicism can cause recurrent transmission ofSCN1A mutations associated with severe myoclonic epilepsy of infancy
Author / Creator:Depienne, Christel ; Arzimanoglou, Alexis ; Trouillard, Oriane ; Fedirko, Estelle ; Baulac, Stéphanie ; Saint-Martin, Cécile ; Ruberg, Merle ; Dravet, Charlotte ; Nabbout, Rima ; Baulac, Michel ; Gourfinkel-An, Isabelle ; Leguern, Eric
Journal title:Human mutation, 2006-04, Vol.27 (4), p.389-389
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ArticlesPeer ReviewedFull Text
Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations
Author / Creator:Moulard, Bruno ; Genton, Pierre ; Grid, Djamel ; Jeanpierre, Marc ; Ouazzani, Réda ; Mrabet, Amel ; Morris, Mike ; LeGuern, Eric ; Dravet, Charlotte ; Mauguière, François ; Utermann, Barbara ; Baldy-Moulinier, Michel ; Belaidi, Halima ; Bertran, Françoise ; Biraben, Arnaud ; Ali Chérif, André ; Chkili, Taieb ; Crespel, Arielle ; Darcel, Françoise ; Dulac, Olivier ; Geny, Christian ; Humbert-Claude, Véronique ; Kassiotis, Philippe ; Buresi, Catherine ; Malafosse, Alain
Publisher:Heidelberg: Springer
Journal title:Human genetics, 2002-09, Vol.111 (3), p.255-262
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Dravet syndrome history

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Different Outcomes of Acute Encephalopathy after Status Epilepticus in Patients with Dravet Syndrome. How to Avoid Them? Comment on De Liso et al. Fatal Status Epilepticus in Dravet Syndrome. Brain Sc...

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Dravet Syndrome: Addressing the Needs of Patients and Families: Introduction

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Dravet Syndrome: Addressing the Needs of Patients and Families: Conclusion

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Unrelated girls share rare disorder

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Tot captures the hearts of emergency crews: FIREFIGHTER ANTHONY BALASTER: ?She's like part of the family to every one of us.?

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Parents' quest aids daughter: They gather, share info about rare disorder

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Parents seek aid for tot with rare disease

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Parents' quest aids daughter: They gather, share info about rare disorder

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Dravet syndrome

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Prognostic Factors for Childhood and Juvenile Absence Epilepsies

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Epilepsy and BRAF Mutations: Phenotypes, Natural History and Genotype-Phenotype Correlations

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Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome

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Parental mosaicism can cause recurrent transmission of SCN1A mutations associated with severe myoclonic epilepsy of infancy

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Treatment of Dravet Syndrome

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Dravet Syndrome: Diagnosis and Long-Term Course

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Helping Families Cope with the Severe Stress of Dravet Syndrome

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Parental mosaicism can cause recurrent transmission ofSCN1A mutations associated with severe myoclonic epilepsy of infancy

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Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations

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