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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Joseph Toulouse

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Neurology. Genetics|December 12, 2018

Delineating FOXG1 syndrome: From congenital microcephaly to hyperkinetic encephalopathyNancy Vegas, Mara Cavallin, Camille Maillard, et al.

Epilepsia|December 27, 2019

Trends in pediatric epilepsy surgery in Europe between 2008 and 2015: Country-, center-, and age-specific variationCarmen Barba, Judith Helen Cross, Kees Braun, et al.

Brain : a Journal of Neurology|June 11, 2021

KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrumClaudia M Bonardi, Henrike O Heyne, Martina Fiannacca, et al.

Medrxiv : the Preprint Server for Health Sciences|September 15, 2025

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.

Nature Genetics|March 30, 2026

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.

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Search research articles

Showing results (11-20 of 15) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 15 results.

Neurology. Genetics|December 12, 2018

Delineating FOXG1 syndrome: From congenital microcephaly to hyperkinetic encephalopathyNancy Vegas, Mara Cavallin, Camille Maillard, et al.

Epilepsia|December 27, 2019

Trends in pediatric epilepsy surgery in Europe between 2008 and 2015: Country-, center-, and age-specific variationCarmen Barba, Judith Helen Cross, Kees Braun, et al.

Brain : a Journal of Neurology|June 11, 2021

KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrumClaudia M Bonardi, Henrike O Heyne, Martina Fiannacca, et al.

Medrxiv : the Preprint Server for Health Sciences|September 15, 2025

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.

Nature Genetics|March 30, 2026

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.

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