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Francesco Fabozzi

Showing results (11-20 of 40) with videos related to

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Frontiers in Cell and Developmental Biology|December 19, 2022
Cerebellar mutism syndrome: From pathophysiology to rehabilitationFrancesco Fabozzi, Stella Margoni, Bianca Andreozzi, et al.
Diagnostics (Basel, Switzerland)|September 28, 2021
Pediatric Extraspinal Sacrococcygeal Ependymoma: Report of Two Cases and Literature ReviewFrancesco Fabozzi, Silvia Ceccanti, Antonella Cacchione, et al.
Recenti Progressi in Medicina|October 2, 2025
Silvia Capuzzi, Federico Baldisseri, Antonella Cacchione, et al.
Clinical Epigenetics|July 7, 2026
Mapping the Safety Profile of Histone Deacetylase Inhibitors in Children with CancerAlessandra Cianflone, Francesco Fabozzi, Fabiana Cacace, et al.
Diagnostics (Basel, Switzerland)|September 23, 2022
Pediatric Diffuse Midline Gliomas: An Unfinished PuzzleValentina Di Ruscio, Giada Del Baldo, Francesco Fabozzi, et al.
JACC. Case Reports|July 18, 2025
Pulmonary Arterial Hypertension After Busulfan Administration During Conditioning Regimen in Neuroblastoma: Key Role of Rescue TreatmentRachele Adorisio, Gessica Ingrasciotta, Francesco Fabozzi, et al.
Diagnostics (Basel, Switzerland)|July 27, 2022
Liquid Biopsy with Detection of NRAS<sup>Q61K</sup> Mutation in Cerebrospinal Fluid: An Alternative Tool for the Diagnosis of Primary Pediatric Leptomeningeal MelanomaAngela Mastronuzzi, Francesco Fabozzi, Martina Rinelli, et al.
Frontiers in Oncology|November 28, 2023
A systematic review of data sources for artificial intelligence applications in pediatric brain tumors in Europe: implications for bias and generalizabilityAlberto Eugenio Tozzi, Ileana Croci, Paul Voicu, et al.
Diagnostics (Basel, Switzerland)|November 11, 2022
Multidisciplinary Management of Craniopharyngiomas in Children: A Single Center ExperienceGiada Del Baldo, Sabina Vennarini, Antonella Cacchione, et al.
Frontiers in Immunology|December 26, 2022
Case report: A new pathogenic variant of LRBA deficiency with a complex phenotype and Rosai-Dorfman diseaseFrancesco Fabozzi, Rita De Vito, Stefania Gaspari, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
Frontiers in Cell and Developmental Biology|December 19, 2022
Cerebellar mutism syndrome: From pathophysiology to rehabilitationFrancesco Fabozzi, Stella Margoni, Bianca Andreozzi, et al.
Diagnostics (Basel, Switzerland)|September 28, 2021
Pediatric Extraspinal Sacrococcygeal Ependymoma: Report of Two Cases and Literature ReviewFrancesco Fabozzi, Silvia Ceccanti, Antonella Cacchione, et al.
Recenti Progressi in Medicina|October 2, 2025
Silvia Capuzzi, Federico Baldisseri, Antonella Cacchione, et al.
Clinical Epigenetics|July 7, 2026
Mapping the Safety Profile of Histone Deacetylase Inhibitors in Children with CancerAlessandra Cianflone, Francesco Fabozzi, Fabiana Cacace, et al.
Diagnostics (Basel, Switzerland)|September 23, 2022
Pediatric Diffuse Midline Gliomas: An Unfinished PuzzleValentina Di Ruscio, Giada Del Baldo, Francesco Fabozzi, et al.
JACC. Case Reports|July 18, 2025
Pulmonary Arterial Hypertension After Busulfan Administration During Conditioning Regimen in Neuroblastoma: Key Role of Rescue TreatmentRachele Adorisio, Gessica Ingrasciotta, Francesco Fabozzi, et al.
Diagnostics (Basel, Switzerland)|July 27, 2022
Liquid Biopsy with Detection of NRAS<sup>Q61K</sup> Mutation in Cerebrospinal Fluid: An Alternative Tool for the Diagnosis of Primary Pediatric Leptomeningeal MelanomaAngela Mastronuzzi, Francesco Fabozzi, Martina Rinelli, et al.
Frontiers in Oncology|November 28, 2023
A systematic review of data sources for artificial intelligence applications in pediatric brain tumors in Europe: implications for bias and generalizabilityAlberto Eugenio Tozzi, Ileana Croci, Paul Voicu, et al.
Diagnostics (Basel, Switzerland)|November 11, 2022
Multidisciplinary Management of Craniopharyngiomas in Children: A Single Center ExperienceGiada Del Baldo, Sabina Vennarini, Antonella Cacchione, et al.
Frontiers in Immunology|December 26, 2022
Case report: A new pathogenic variant of LRBA deficiency with a complex phenotype and Rosai-Dorfman diseaseFrancesco Fabozzi, Rita De Vito, Stefania Gaspari, et al.
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