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Publications by Nelia Zamponi

Clinical and Genetic Factors Predicting Dravet Syndrome in Infants With SCN1A Mutations

English

Rufinamide for Refractory Focal Seizures: An Open-Label, Multicenter European Study

Seizure : the journal of the British Epilepsy Association

English

Related publications

Dravet Syndrome: Patients With Co-Morbid SCN1A Gene Mutations and Mitochondrial Electron Transport Chain Defects

Seizure : the journal of the British Epilepsy Association

English

Analysis of SCN1A Mutation and Parental Origin in Patients With Dravet Syndrome

Journal of Human Genetics

English

Drug Screening in Scn1a Zebrafish Mutant Identifies Clemizole as a Potential Dravet Syndrome Treatment

Nature Communications

Molecular Biology

English

Expecting the Unexpected: Lack of in Vivo Network Defects in an Scn1a Model of Dravet Syndrome

Epilepsy Currents

English

The Contribution of CACNA1A, ATP1A2 and SCN1A Mutations in Hemiplegic Migraine: A Clinical and Genetic Study in Finnish Migraine Families

English

Wolcott-Rallison Syndrome: Clinical, Genetic, and Functional Study of EIF2AK3 Mutations and Suggestion of Genetic Heterogeneity

Internal Medicine

English

Perineal Stimulation Triggering Seizures in a Child With Dravet Syndrome

Seizure : the journal of the British Epilepsy Association

English

Dravet Syndrome: Characteristics, Comorbidities, and Caregiver Concerns

Epilepsy and Behavior

Behavioral Neuroscience

English

Clinical Exome Sequencing Identifies Two Novel Mutations of the SCN1A and SCN2A Genes in Moroccan Patients With Epilepsy: A Case Series

Journal of Medical Case Reports

English