Elisabetta Di Fede
Milan, 20142, Italy
Last Updated: 09/26/2026
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Found 21 publications
Interleukin-8 and extracellular vesicles spread senescence in Lymphangioleiomyomatosis microenvironment.
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Published: February 13, 2026
Portrait of a Spectrum: Clinical and Genetic Characterization of a Large Cohort of Chromatinopathies-30 Years' Experience From a Third Level Center.
Journal: Clinical genetics
Published: August 06, 2025
Exploring the uncharted role of cell senescence in rare diseases.
Journal: Orphanet journal of rare diseases
Published: December 18, 2024
Expanding the clinical spectrum of PPP3CA variants - alternative isoforms matter.
Journal: Orphanet journal of rare diseases
Published: November 15, 2024
Intrauterine growth in chromatinopathies: A long road for better understanding and for improving clinical management.
Journal: Birth defects research
Published: February 23, 2024
Characterization of a novel HDAC2 pathogenetic variant: a missing puzzle piece for chromatinopathies.
Journal: Human genetics
Published: November 19, 2023
Epigenetic disorders: Lessons from the animals-animal models in chromatinopathies.
Journal: Frontiers in cell and developmental biology
Published: June 27, 2022
Identical EP300 variant leading to Rubinstein-Taybi syndrome with different clinical and immunologic phenotype.
Journal: American journal of medical genetics. Part A
Published: April 26, 2021
SLC35F1 as a candidate gene for neurodevelopmental disorders resembling Rett syndrome.
Journal: American journal of medical genetics. Part A
Published: March 22, 2021
Last Updated: 09/26/2026