Eva Andermann

Montreal, QC, Canada

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 32 publications

Diverse Genetic Etiologies of Unilateral Polymicrogyria.

Diverse Genetic Etiologies of Unilateral Polymicrogyria.

Journal: Annals of neurology

Published: May 20, 2025

Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria.

Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria.

Journal: JAMA neurology

Published: July 24, 2023

Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes.

Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes.

Journal: American journal of human genetics

Published: June 29, 2020

Comparative analysis of the safety and tolerability of eslicarbazepine acetate in older (≥60 years) and younger (18-59 years) adults.

Comparative analysis of the safety and tolerability of eslicarbazepine acetate in older (≥60 years) and younger (18-59 years) adults.

Journal: Epilepsy research

Published: March 10, 2020

Autosomal-dominant adult neuronal ceroid lipofuscinosis caused by duplication in DNAJC5 initially missed by Sanger and whole-exome sequencing.

Autosomal-dominant adult neuronal ceroid lipofuscinosis caused by duplication in DNAJC5 initially missed by Sanger and whole-exome sequencing.

Journal: European journal of human genetics : EJHG

Published: May 03, 2019

Duplication 2p16 is associated with perisylvian polymicrogyria.

Duplication 2p16 is associated with perisylvian polymicrogyria.

Journal: American journal of medical genetics. Part A

Published: December 19, 2018

Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features.

Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features.

Journal: Brain : a journal of neurology

Published: August 06, 2018

Evidence of linkage to chromosome 5p13.2-q11.1 in a large inbred family with genetic generalized epilepsy.

Evidence of linkage to chromosome 5p13.2-q11.1 in a large inbred family with genetic generalized epilepsy.

Journal: Epilepsia

Published: June 06, 2018

Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development.

Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development.

Journal: Neuron

Published: December 28, 2017

Psychiatric and cognitive adverse events: A pooled analysis of three phase III trials of adjunctive eslicarbazepine acetate for partial-onset seizures.

Psychiatric and cognitive adverse events: A pooled analysis of three phase III trials of adjunctive eslicarbazepine acetate for partial-onset seizures.

Journal: Epilepsy & behavior : E&B

Published: April 26, 2017

Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties.

Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties.

Journal: Annals of neurology

Published: November 17, 2016

Myoclonus and seizures in progressive myoclonus epilepsies: pharmacology and therapeutic trials.

Myoclonus and seizures in progressive myoclonus epilepsies: pharmacology and therapeutic trials.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: September 16, 2016

Showing 1-12 of 32

Last Updated: 09/26/2026