Valentina Cetica
Florence, 50139, Italy
Last Updated: 09/26/2026
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Found 29 publications
Optimized nuclei isolation and snRNA-seq reveal oligodendrocyte pathway dysregulation in MOGHE brain tissue from pediatric patients.
Journal: Scientific reports
Published: February 02, 2026
Clinico-pathological and molecular characteristics of pediatric-juvenile pituitary neuroendocrine tumors (PitNETs): A mono-institutional series.
Journal: Clinical neuropathology
Published: June 02, 2025
RICTOR variants are associated with neurodevelopmental disorders.
Journal: European journal of human genetics : EJHG
Published: August 01, 2024
Double gonosomal mosaicism as an unusual hereditary mechanism in familial GRIN2A-related disorder.
Journal: Journal of medical genetics
Published: May 03, 2024
Clinical and molecular characterization of patients with YWHAG-related epilepsy.
Journal: Epilepsia
Published: November 10, 2023
Bilateral temporal lobe dysplasia and seizure onset associated with biallelic CNTNAP2 variants.
Journal: Epilepsia open
Published: July 31, 2023
Leat-associated seizures the possible role of EAAT2, pyruvate carboxylase and glutamine synthetase.
Journal: Epilepsy research
Published: May 23, 2023
Confirmation of the Pathogenetic Role of the CCDC88C Gene in Early-Onset Pure Spastic Paraplegia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: April 04, 2023
Fetal Presentation of Walker-Warburg Syndrome with Compound Heterozygous POMT2 Missense Mutations.
Journal: Fetal and pediatric pathology
Published: September 01, 2022
Myxoid glioneuronal tumor: Histopathologic, neuroradiologic, and molecular features in a single center series.
Journal: Neoplasia (New York, N.Y.)
Published: August 29, 2022
Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the SLC35A2 Gene.
Journal: Neurology
Published: May 03, 2022
Last Updated: 09/26/2026