Valerio Conti

7PUBLICATIONS
63CO-AUTHORS
Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Medical infection agents (incl. prions)Infant and child health
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Publications (7)

|Aug 06, 2026
Associations of Cortical and Subcortical White Matter Morphometric Abnormalities With Clinical and Genetic Findings in STXBP1 Encephalopathy.

|Dec 11, 2025
SLC35A2-Related Brain Disorders: Genetics, Pathophysiology, and Therapeutic Insights.

Beatrice Risso, Antonella Riva, Greta Volpedo

|Oct 13, 2025
Mosaic expression of SLC35A2 pathogenetic variants impairs neuronal migration and dendritogenesis in the developing cortex.

Antonio Falace, Léa Corbières, Lucas Silvagnoli

|Apr 23, 2022
Prospective Evaluation of Ghrelin and Des-Acyl Ghrelin Plasma Levels in Children with Newly Diagnosed Epilepsy: Evidence for Reduced Ghrelin-to-Des-Acyl Ghrelin Ratio in Generalized Epilepsies.

Anna-Maria Costa, Tommaso Lo Barco, Elisabetta Spezia

|Feb 05, 2021
Is Focal Cortical Dysplasia/Epilepsy Caused by Somatic MTOR Mutations Always a Unilateral Disorder?

Renzo Guerrini, Mara Cavallin, Tommaso Pippucci

|Sep 08, 2020
International consensus recommendations on the diagnostic work-up for malformations of cortical development.

Renske Oegema, Tahsin Stefan Barakat, Martina Wilke

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Frequent Collaborators

4 joint publications

Renzo Guerrini

2 joint publications

Antonio Falace

2 joint publications

Elena Parrini

2 joint publications

Francesca Darra