Evelina Carapancea

5PUBLICATIONS
86CO-AUTHORS
Infant and child healthGene expression (incl. microarray and other genome-wide approaches)Micro-manipulationDevelopmental genetics (incl. sex determination)Neonatology
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Publications (5)

|Aug 10, 2026
Diagnostic delay in infants with very early-onset rare and ultra-rare genetic epilepsies.

|Jan 28, 2026
Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variants.

Sebastian Ortiz, Leonardo Affronte, Chiara Bagliani

|Sep 16, 2025
Everolimus precision therapy in NPRL2- and NPRL3-related epilepsy.

Evelina Carapancea, Erik A Eklund, Helene Verhelst

|Jun 30, 2025
Epilepsy phenotype and developmental outcome in girls with mosaicism in X-linked neurodevelopmental disorders.

Evelina Carapancea, Donya Eizadkhah, Roberto Santalucia

|Jan 04, 2023
Clinical and Neurophysiologic Phenotypes in Neonates With BRAT1 Encephalopathy.

Evelina Carapancea, Marie-Coralie Cornet, Mathieu Milh

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Frequent Collaborators

5 joint publications

Maria Roberta Cilio

3 joint publications

Damien Lederer

2 joint publications

Pasquale Striano

2 joint publications

Renzo Guerrini