Veronica Saletti
Milan, Italy
Last Updated: 09/26/2026
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Found 64 publications
Papillary Tumour of the Pineal Region, in a Child With a Germline PTEN Pathogenic Variant, Arisen in the Fourth Ventricle.
Journal: Neuropathology and applied neurobiology
Published: May 15, 2026
Sylvian Fissure Meningioma in a Child With KRAS-Related Noonan Syndrome.
Journal: Pediatric neurology
Published: March 26, 2026
Pharmacokinetics and Safety of Selumetinib Granule Formulation in Children With Symptomatic, Inoperable Neurofibromatosis Type 1-Related Plexiform Neurofibromas (SPRINKLE; phase I/II).
Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Published: January 27, 2026
Social and subjective representations of visual impairment in Italy: a qualitative study.
Journal: BMJ paediatrics open
Published: October 30, 2025
Teaching NeuroImage: Distinctive White Matter Abnormalities in KIF1C Pathogenic Variants.
Journal: Neurology
Published: August 07, 2025
Which type of duraplasty is best for Chiari type I malformation surgery?
Journal: Neurosurgical focus
Published: September 15, 2024
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes.
Journal: Human genetics
Published: March 15, 2024
Quality of life, functioning and participation of children and adolescents with visual impairment: A scoping review.
Journal: Research in developmental disabilities
Published: March 15, 2024
Chiari Malformation Type 1 and Syringomyelia: Why Do Patients Claim for International Guidelines? Commentary on the 2021 Chiari and Syringomyelia Consensus Document.
Journal: Acta neurochirurgica. Supplement
Published: December 28, 2023
Evaluation of Adult and Pediatric Chiari Type 1 Malformation Patients: Do Consensus Documents Fit Everyday Practice?
Journal: Acta neurochirurgica. Supplement
Published: December 28, 2023
Surgical Management of Chiari 1.5 in Children: A Truly Different Disease?
Journal: Journal of clinical medicine
Published: November 21, 2023
Case report: SLC6A1 mutations presenting with isolated absence seizures: description of 2 novel cases.
Journal: Frontiers in neuroscience
Published: May 08, 2023
Last Updated: 09/26/2026