Ferdinando Aliberti

Naples, Italy

Last Updated: 09/26/2026

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Found 22 publications

XLH Matters: an evolving programme to discuss new advances and share clinical experiences to improve patient outcomes.

XLH Matters: an evolving programme to discuss new advances and share clinical experiences to improve patient outcomes.

Journal: Orphanet journal of rare diseases
Published: February 03, 2025

Correction: Biobank for craniosynostosis and faciocraniosynostosis, rare pediatric congenital craniofacial disorders: a study protocol.

Correction: Biobank for craniosynostosis and faciocraniosynostosis, rare pediatric congenital craniofacial disorders: a study protocol.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: September 23, 2024

Neuroimaging in Nonsyndromic Craniosynostosis: Key Concepts to Unlock Innovation.

Neuroimaging in Nonsyndromic Craniosynostosis: Key Concepts to Unlock Innovation.

Journal: Diagnostics (Basel, Switzerland)
Published: July 01, 2024

Biobank for craniosynostosis and faciocraniosynostosis, rare pediatric congenital craniofacial disorders: a study protocol.

Biobank for craniosynostosis and faciocraniosynostosis, rare pediatric congenital craniofacial disorders: a study protocol.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: October 24, 2023

Changes in venous drainage after posterior cranial vault distraction and foramen magnum decompression in syndromic craniosynostosis.

Changes in venous drainage after posterior cranial vault distraction and foramen magnum decompression in syndromic craniosynostosis.

Journal: Journal of neurosurgery. Pediatrics
Published: May 03, 2022

Dural venous sinus anatomy in children with external hydrocephalus: analysis of a series of 97 patients.

Dural venous sinus anatomy in children with external hydrocephalus: analysis of a series of 97 patients.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: June 12, 2021

A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndrome.

A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndrome.

Journal: European journal of medical genetics
Published: December 04, 2020

Endoscopic aqueductoplasty and stenting in the treatment of isolated fourth ventricle in children: 20-year institutional experience.

Endoscopic aqueductoplasty and stenting in the treatment of isolated fourth ventricle in children: 20-year institutional experience.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: September 06, 2020

Brain Herniation into the Subdural Space: Rare Iatrogenic Complication of Treatment of a Giant Calcified Subdural Hematoma.

Brain Herniation into the Subdural Space: Rare Iatrogenic Complication of Treatment of a Giant Calcified Subdural Hematoma.

Journal: World neurosurgery
Published: April 19, 2020

Temporal lobe malformations, focal epilepsy, and FGFR3 mutations: a non-causal association?

Temporal lobe malformations, focal epilepsy, and FGFR3 mutations: a non-causal association?

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: January 30, 2020

Myofibroma-A Common Congenital Lesion.

Myofibroma-A Common Congenital Lesion.

Journal: The Journal of pediatrics
Published: April 17, 2019

Endoscopic ultrasonic aspiration of brain abscess.

Endoscopic ultrasonic aspiration of brain abscess.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: May 24, 2018
Showing 1-12 of 22

Last Updated: 09/26/2026