Nathalie Roeckel-Trévisiol

Large-scale expression study of human mesial temporal lobe epilepsy: evidence for dysregulation of the neurotransmission and complement systems in the entorhinal cortex.

J. Régis, P. Chauvel, F. Bartolomei, 2006, Brain : a journal of neurology.

SRPX2 mutations in disorders of language cortex and cognition.

Marie-Noëlle Metz-Lutz, Edouard Hirsch, Sandrine Pereira, 2006, Human molecular genetics.

Nuclear localization of a novel human syntaxin 1B isoform.

N. Lévy, P. Pontarotti, C. Lévêque, 2008, Gene.

Imbalance of NRG1-ERBB2/3 signalling underlies altered myelination in Charcot–Marie–Tooth disease 4H

A. Mégarbané, J. Borg, N. Lévy, 2022, Brain : a journal of neurology.

Imbalance of Neuregulin1-ErbB2/3 signaling underlies altered myelin homeostasis in models of Charcot-Marie-Tooth disease type 4H

A. Mégarbané, J. Borg, N. Lévy, 2022, bioRxiv.

Functional Variant in Complement C3 Gene Promoter and Genetic Susceptibility to Temporal Lobe Epilepsy and Febrile Seizures

A. Malafosse, A. Crespel, E. Pataraia, 2010, PloS one.