Giulia Gori
Florence, Italy
Last Updated: 09/26/2026
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Found 11 publications
A Novel Epilepsy Phenotype in a Young Girl With a Pathogenic SETD5 Gene Variant.
Journal: Journal of child neurology
Published: June 04, 2025
Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver-Russell Syndrome and Focus on the IGF1R Gene.
Journal: The Journal of clinical endocrinology and metabolism
Published: June 26, 2024
Endocrinological features and epileptic encephalopathy in COX deficiency due to SCO1 mutations: case series and review of literature.
Journal: Endocrine connections
Published: June 14, 2024
A novel bioinformatic method for the identification of antimicrobial peptides in metagenomes.
Journal: Journal of applied microbiology
Published: November 13, 2023
SMARCE1-related meningiomas: A clear example of cancer predisposing syndrome.
Journal: European journal of medical genetics
Published: December 19, 2022
FOXI3 pathogenic variants cause one form of craniofacial microsomia.
Journal: Nature communications
Published: April 09, 2022
Carriers of ADAMTS13 Rare Variants Are at High Risk of Life-Threatening COVID-19.
Journal: Viruses
Published: March 21, 2022
Genetic counseling during COVID-19 pandemic: Tuscany experience.
Journal: Molecular genetics & genomic medicine
Published: May 29, 2020
A bioreactor with an electro-responsive elastomeric membrane for mimicking intestinal peristalsis.
Journal: Bioinspiration & biomimetics
Published: December 06, 2016
Polymeric Microporous Nanofilms as Smart Platforms for in Vitro Assessment of Nanoparticle Translocation and Caco-2 Cell Culture.
Journal: IEEE transactions on nanobioscience
Published: August 31, 2016
Showing 1-11 of 11
Last Updated: 09/26/2026