Valentina Imperatore
5PUBLICATIONS
20CO-AUTHORS
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Publications (5)
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|Mar 28, 2026
SINEUP-Mediated Overexpression of Endogenous α-Amylase as a Therapeutic Approach in Lafora Disease.Lorenzo Allegri, Federica Baldan, Catia Mio
|Nov 13, 2025
Usmani-Riazuddin Syndrome: Functional Characterization of a Novel c.196G>A Variant in the AP1G1 Gene and Phenotypic Insights Using Zebrafish as a Vertebrate Model.Valentina Imperatore, Alessandra Mirarchi, Emanuele Agolini
|Sep 28, 2021
A Rare Case of Brachyolmia with Amelogenesis Imperfecta Caused by a New Pathogenic Splicing Variant in LTBP3.Elisabetta Flex, Valentina Imperatore, Giovanna Carpentieri
|Aug 27, 2021
Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome.Kathleen Rooney, Michael A Levy, Sadegheh Haghshenas
|Jan 14, 2021
Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype.Maria Giovanna Tedesco, Fortunato Lonardo, Caterina Ceccarini
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Frequent Collaborators
2 joint publications
Paolo Prontera
2 joint publications
Giuseppe Merla
1 joint publications
Chiara Leoni
1 joint publications
Maria Teresa Falco
1 joint publications
Paolo Fontana
1 joint publications
Kathleen Rooney
1 joint publications
Jennifer Kerkhof
1 joint publications
Matthew L Tedder
1 joint publications
Elisabetta Flex
1 joint publications
Marco Tartaglia
