Gaia Fusto
Catania, 95123, Italy
Last Updated: 09/26/2026
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Found 8 publications
WWOX-Related Epileptic Encephalopathy (WOREE Syndrome): Clinical Case Study and Literature Review.
Journal: Current issues in molecular biology
Published: March 15, 2026
Chromothriptic Translocation t(1;18): A Paradigm of Genomic Complexity in a Child with Normal Intellectual Development and Pyridoxine-Dependent Epilepsy.
Journal: Genes
Published: October 21, 2025
Molecular and Neurobiological Imbalance from the Use of Technological Devices During Early Child Development Stages.
Journal: Children (Basel, Switzerland)
Published: May 30, 2025
The Many Faces of Child Abuse: How Clinical, Genetic and Epigenetic Correlates Help Us See the Full Picture.
Journal: Children (Basel, Switzerland)
Published: May 07, 2025
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1.
Journal: Clinical and experimental pediatrics
Published: February 09, 2025
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy?
Journal: Molecular and cellular pediatrics
Published: November 12, 2024
GLUT-1DS resistant to ketogenic diet: from clinical feature to in silico analysis. An exemplificative case report with a literature review.
Journal: Neurogenetics
Published: November 20, 2023
Showing 1-8 of 8
Last Updated: 09/26/2026