Lorena Travaglini

4PUBLICATIONS
44CO-AUTHORS
Developmental genetics (incl. sex determination)Gene expression (incl. microarray and other genome-wide approaches)Autonomic nervous system
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Publications (4)

|Jun 20, 2024
Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders.

Juan Darío Ortigoza-Escobar, Mina Zamani, Nathalie Dorison

|May 17, 2022
"Atypical" Krabbe disease in two siblings harboring biallelic GALC mutations including a deep intronic variant.

Francesco Nicita, Fabrizia Stregapede, Federica Deodato

|Nov 08, 2021
Clinical variability at the mild end of BRAT1-related spectrum: Evidence from two families with genotype-phenotype discordance.

Sara Nuovo, Valentina Baglioni, Roberta De Mori

|Nov 10, 2019
Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutation.

Fabrizia Stregapede, Lorena Travaglini, Adriana P Rebelo

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Frequent Collaborators

3 joint publications

Francesco Nicita

1 joint publications

Sara Nuovo

1 joint publications

Valentina Baglioni

1 joint publications

Roberta De Mori