Fabio Acquaviva
4PUBLICATIONS
19CO-AUTHORS
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Publications (4)
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|Sep 13, 2025
Early Diagnosis and Follow-Up of a Novel Homozygous Mutation in SOST Gene in a Child with Recurrent Facial Palsy: A Case Report and Review of the Literature.Fabio Acquaviva, Giorgia Bruno, Federica Palladino
|May 25, 2024
Comprehensive Molecular Analysis of Disease-Related Genes as First-Tier Test for Early Diagnosis, Classification, and Management of Patients Affected by Nonsyndromic Ichthyosis.Tiziana Fioretti, Fabrizio Martora, Ilaria De Maggio
|Oct 27, 2022
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum.Francesco Passaretti, Laura Pignata, Giuseppina Vitiello
|Aug 27, 2021
Fibrodysplasia Ossificans Progressiva: A Challenging Diagnosis.Daniele De Brasi, Francesca Orlando, Valeria Gaeta
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Frequent Collaborators
2 joint publications
Daniele De Brasi
1 joint publications
Daniele De Brasi
1 joint publications
Francesco Passaretti
1 joint publications
Laura Pignata
1 joint publications
Viola Alesi
1 joint publications
Antonio Novelli
1 joint publications
Andrea Riccio
1 joint publications
Achille Iolascon
1 joint publications
Flavia Cerrato
1 joint publications
Fabrizio Martora
