Silvia Napuri

Rennes, France

Last Updated: 09/26/2026

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Found 11 publications

Early sodium channel blocker initiation is associated with better outcomes in KCNQ2 disorders.

Early sodium channel blocker initiation is associated with better outcomes in KCNQ2 disorders.

Journal: Brain : a journal of neurology

Published: October 17, 2025

The Difficult Journey of a Child with Dravet Syndrome: Perspectives from a Parent and the Neuropaediatrician.

The Difficult Journey of a Child with Dravet Syndrome: Perspectives from a Parent and the Neuropaediatrician.

Journal: Neurology and therapy

Published: June 19, 2025

Clinical and Neurodevelopmental Characteristics of Paralogous Gain-of-Function Variants at GRIA2 p.Gly792 and GRIA3 p.Gly803.

Clinical and Neurodevelopmental Characteristics of Paralogous Gain-of-Function Variants at GRIA2 p.Gly792 and GRIA3 p.Gly803.

Journal: Clinical genetics

Published: October 28, 2024

Interhemispheric coherence of EEG rhythms in children: Maturation and differentiation in corpus callosum dysgenesis.

Interhemispheric coherence of EEG rhythms in children: Maturation and differentiation in corpus callosum dysgenesis.

Journal: Neurophysiologie clinique = Clinical neurophysiology

Published: February 21, 2024

Phosphatidylserine enriched with polyunsaturated n-3 fatty acid supplementation for attention-deficit hyperactivity disorder in children and adolescents with epilepsy: A randomized placebo-controlled trial.

Phosphatidylserine enriched with polyunsaturated n-3 fatty acid supplementation for attention-deficit hyperactivity disorder in children and adolescents with epilepsy: A randomized placebo-controlled trial.

Journal: Epilepsia open

Published: May 10, 2023

Tuberous sclerosis complex and epilepsy in infancy: prevention and early diagnosis.

Tuberous sclerosis complex and epilepsy in infancy: prevention and early diagnosis.

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: December 30, 2022

Progressive Leukodystrophy-Like Demyelinating Syndromes with MOG-Antibodies in Children: A Rare Under-Recognized Phenotype.

Progressive Leukodystrophy-Like Demyelinating Syndromes with MOG-Antibodies in Children: A Rare Under-Recognized Phenotype.

Journal: Neuropediatrics

Published: April 01, 2021

ADHD in childhood epilepsy: Clinical determinants of severity and of the response to methylphenidate.

ADHD in childhood epilepsy: Clinical determinants of severity and of the response to methylphenidate.

Journal: Epilepsia

Published: April 25, 2016

Epilepsy in young Tsc1(+/-) mice exhibits age-dependent expression that mimics that of human tuberous sclerosis complex.

Epilepsy in young Tsc1(+/-) mice exhibits age-dependent expression that mimics that of human tuberous sclerosis complex.

Journal: Epilepsia

Published: January 04, 2016

Chronic Diarrhea in L-Amino Acid Decarboxylase (AADC) Deficiency: A Prominent Clinical Finding Among a Series of Ten French Patients.

Chronic Diarrhea in L-Amino Acid Decarboxylase (AADC) Deficiency: A Prominent Clinical Finding Among a Series of Ten French Patients.

Journal: JIMD reports

Published: September 24, 2015

Topography of brain damage in metabolic hypoglycaemia is determined by age at which hypoglycaemia occurred.

Topography of brain damage in metabolic hypoglycaemia is determined by age at which hypoglycaemia occurred.

Journal: Developmental medicine and child neurology

Published: December 05, 2012

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Last Updated: 09/26/2026