Francesca Peluso

7PUBLICATIONS
36CO-AUTHORS
Infant and child healthNeurogeneticsChild language acquisitionOther language, communication and culture not elsewhere classifiedEpigenetics (incl. genome methylation and epigenomics)
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Publications (7)

|Jan 10, 2026
Feeding-Triggered Seizures in a Newborn with <i>AP1S1</i>-Related MEDNIK Syndrome: Expanding the Phenotype of a Hyper-Rare Disease.

Anna Cavalli, Francesca Peluso, Daniele Frattini

|Feb 26, 2025
Expanding the mutational spectrum of ReNU syndrome: insights into 5' Stem-loop variants.

Alessandro Bruselles, Cecilia Mancini, Luigi Chiriatti

|Aug 20, 2024
An uncommon neuroradiological finding of hippocampal malrotation in childhood onset schizophrenia and 22q11.2 Deletion Syndrome: a case report and a brief review of the literature.

Maria Giardino, Francesca Peluso, Omar Daolio

|Aug 26, 2023
Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the <i>DLX5/6</i> Genes.

Irene Ambrosetti, Laura Bernardini, Marzia Pollazzon

|Aug 16, 2023
Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature.

Francesca Peluso, Stefano G Caraffi, Gianluca Contrò

|Mar 29, 2023
Prenatal Clinical Findings in <i>RASA1</i>-Related Capillary Malformation-Arteriovenous Malformation Syndrome.

Emanuele Coccia, Lara Valeri, Roberta Zuntini

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Frequent Collaborators

3 joint publications

Stefano Giuseppe Caraffi

3 joint publications

Antonio Novelli

2 joint publications

Francesca Clementina Radio

2 joint publications

Marco Tartaglia