Stéphane Auvin
0000-0003-3874-9749
19 papers found
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Call for the use of the ILAE terminology for seizures and epilepsies by health care professionals and regulatory agencies to benefit patients and caregivers
Medical treatment in infants and young children with epilepsy: Off‐label use of antiseizure medications. Survey Report of ILAE Task Force Medical Therapies in Children
ILAE definition of the Idiopathic Generalized Epilepsy Syndromes: Position statement by the ILAE Task Force on Nosology and Definitions
International League Against Epilepsy classification and definition of epilepsy syndromes with onset at a variable age: position statement by the ILAE Task Force on Nosology and Definitions
ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions
International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and Definitions
Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in Europe
Glut1 Deficiency Syndrome (Glut1DS): state of the art in 2020 and recommendations of the international Glut1DS study group
Homozygous GRN mutations: new phenotypes and new insights into pathological and molecular mechanisms
Novel study design to assess the efficacy and tolerability of antiseizure medications for focal‐onset seizures in infants and young children: A consensus document from the regulatory task force and the pediatric commission of the International League against Epilepsy (ILAE), in collaboration with the Pediatric Epilepsy Research Consortium (PERC)
Systematic review of the screening, diagnosis, and management of ADHD in children with epilepsy. Consensus paper of the Task Force on Comorbidities of the ILAE Pediatric Commission
A common language of seizures and epilepsies: International League Against Epilepsy 2017 classifications
Prediction of responders to ketogenic diet based on syndrome and etiology: identification of a new target population?
Functional ultrasound imaging of brain activity in human newborns
Anti-ictogenic and antiepileptogenic properties of perampanel in mature and immature rats
Épilepsie absence de l’enfant : actualités diagnostiques et thérapeutiques
An unfortunate challenge: Ketogenic diet for the treatment of Lennox-Gastaut syndrome in Tyrosinemia type 1
Late onset epileptic spasms is frequent in MECP2 gene duplication: Electroclinical features and long-term follow-up of 8 epilepsy patients
Should we still consider Dravet syndrome an epileptic encephalopathy?
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