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World Journal of Clinical Cases
|
November 16, 2020
Dehydrated patient without clinically evident cause: A case report
Federica 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 syndrome
Claudia 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 report
Claudia 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 Italy
Federica 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 Literature
Fabio 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 1
Claudia 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 Analysis
Camilla 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 peritonei
Nayana Lazzari, Giulia Rigotto, Barbara Montini, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
World Journal of Clinical Cases
|
November 16, 2020
Dehydrated patient without clinically evident cause: A case report
Federica 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 syndrome
Claudia 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 report
Claudia 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 Italy
Federica 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 Literature
Fabio 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 1
Claudia 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 Analysis
Camilla 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 peritonei
Nayana Lazzari, Giulia Rigotto, Barbara Montini, et al.
Page
of 1