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Federica Palladino

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World Journal of Clinical Cases|November 16, 2020
Dehydrated patient without clinically evident cause: A case reportFederica Palladino, Maria Cristina Fedele, Marianna Casertano, et al.
European Journal of Medical Genetics|March 16, 2021
A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndromeClaudia Santoro, Simona Riccio, Federica Palladino, et al.
BMC Neurology|September 3, 2020
A novel RAB39B mutation and concurrent de novo NF1 mutation in a boy with neurofibromatosis type 1, intellectual disability, and autism: a case reportClaudia Santoro, Teresa Giugliano, Pia Bernardo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 23, 2020
Is Covid-19 lockdown related to an increase of accesses for seizures in the emergency department? An observational analysis of a paediatric cohort in the Southern ItalyFederica Palladino, Eugenio Merolla, Marella Solimeno, et al.
International Journal of Molecular Sciences|September 13, 2025
Early Diagnosis and Follow-Up of a Novel Homozygous Mutation in <i>SOST</i> Gene in a Child with Recurrent Facial Palsy: A Case Report and Review of the LiteratureFabio Acquaviva, Giorgia Bruno, Federica Palladino, et al.
Cancers|June 4, 2020
Retrospective Multicentric Study on Non-Optic CNS Tumors in Children and Adolescents with Neurofibromatosis Type 1Claudia Santoro, Stefania Picariello, Federica Palladino, et al.
Journal of Clinical Medicine|November 13, 2025
Cortical Tubers' Transformation in Pediatric Patients Diagnosed with Tuberous Sclerosis Complex: A Retrospective Longitudinal MRI AnalysisCamilla Russo, Simone Coluccino, Maria Fulvia De Leva, et al.
International Journal of Cancer|August 15, 2024
Stemness and hybrid epithelial-mesenchymal profiles guide peritoneal dissemination of malignant mesothelioma and pseudomyxoma peritoneiNayana Lazzari, Giulia Rigotto, Barbara Montini, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
World Journal of Clinical Cases|November 16, 2020
Dehydrated patient without clinically evident cause: A case reportFederica Palladino, Maria Cristina Fedele, Marianna Casertano, et al.
European Journal of Medical Genetics|March 16, 2021
A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndromeClaudia Santoro, Simona Riccio, Federica Palladino, et al.
BMC Neurology|September 3, 2020
A novel RAB39B mutation and concurrent de novo NF1 mutation in a boy with neurofibromatosis type 1, intellectual disability, and autism: a case reportClaudia Santoro, Teresa Giugliano, Pia Bernardo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 23, 2020
Is Covid-19 lockdown related to an increase of accesses for seizures in the emergency department? An observational analysis of a paediatric cohort in the Southern ItalyFederica Palladino, Eugenio Merolla, Marella Solimeno, et al.
International Journal of Molecular Sciences|September 13, 2025
Early Diagnosis and Follow-Up of a Novel Homozygous Mutation in <i>SOST</i> Gene in a Child with Recurrent Facial Palsy: A Case Report and Review of the LiteratureFabio Acquaviva, Giorgia Bruno, Federica Palladino, et al.
Cancers|June 4, 2020
Retrospective Multicentric Study on Non-Optic CNS Tumors in Children and Adolescents with Neurofibromatosis Type 1Claudia Santoro, Stefania Picariello, Federica Palladino, et al.
Journal of Clinical Medicine|November 13, 2025
Cortical Tubers' Transformation in Pediatric Patients Diagnosed with Tuberous Sclerosis Complex: A Retrospective Longitudinal MRI AnalysisCamilla Russo, Simone Coluccino, Maria Fulvia De Leva, et al.
International Journal of Cancer|August 15, 2024
Stemness and hybrid epithelial-mesenchymal profiles guide peritoneal dissemination of malignant mesothelioma and pseudomyxoma peritoneiNayana Lazzari, Giulia Rigotto, Barbara Montini, et al.
Pageof 1