Marie-anne J. Barthez
Tours, France
Last Updated: 09/26/2026
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Found 8 publications
Transition from pediatric to adult care system in patients with complex epilepsies: Necker model for transition evaluated on 70 consecutive patients.
Journal: Epilepsia
Published: August 12, 2024
West Syndrome Is an Exceptional Presentation of Pyridoxine- and Pyridoxal Phosphate-Dependent Epilepsy: Data From a French Cohort and Review of the Literature.
Journal: Frontiers in pediatrics
Published: October 25, 2020
Epilepsy with migrating focal seizures: KCNT1 mutation hotspots and phenotype variability.
Journal: Neurology. Genetics
Published: December 22, 2018
KCNT1 epilepsy with migrating focal seizures shows a temporal sequence with poor outcome, high mortality and SUDEP.
Journal: Brain : a journal of neurology
Published: November 21, 2018
Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 21, 2018
Children often present with infantile spasms after herpetic encephalitis.
Journal: Epilepsia
Published: May 22, 2013
TCTN3 mutations cause Mohr-Majewski syndrome.
Journal: American journal of human genetics
Published: March 05, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026