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Raffaele Falsaperla

Showing results (151-160 of 251) with videos related to

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Journal of Pediatric Genetics|July 28, 2020
Primary Microcephaly with Novel Variant of <i>MCPH1</i> Gene in Twins: Both Manifesting in Childhood at the Same Time with Hashimoto's ThyroiditisPiero Pavone, Xena Giada Pappalardo, Andrea Domenico Praticò, et al.
Frontiers in Pediatrics|October 12, 2020
Intronic Variant in <i>CNTNAP2</i> Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and SeizuresRaffaele Falsaperla, Xena Giada Pappalardo, Catia Romano, et al.
Children (Basel, Switzerland)|September 28, 2021
The Evolution of the Role of Imaging in the Diagnosis of Craniosynostosis: A Narrative ReviewGiovanni Cacciaguerra, Monica Palermo, Lidia Marino, et al.
Clinical and Experimental Vaccine Research|August 15, 2024
SARS-CoV-2 parental vaccination and risk of multisystem inflammatory syndrome in children: a single-center retrospective studyRaffaele Falsaperla, Vincenzo Sortino, Ausilia Desiree Collotta, et al.
Children (Basel, Switzerland)|May 27, 2023
SARS-CoV-2 and Swabs: Disease Severity and the Numbers of Cycles of Gene Amplification, Single Center ExperienceRaffaele Falsaperla, Vincenzo Sortino, Ausilia Desiree Collotta, et al.
World Neurosurgery|June 6, 2022
Decision-Making Challenge of Ping-Pong Fractures in Children: Case Exemplification and Systematic Review of LiteratureRoberto Altieri, Erica Grasso, Giacomo Cammarata, et al.
Neuropsychiatric Disease and Treatment|June 16, 2017
Ictal blinking, an under-recognized phenomenon: our experience and literature reviewMarco Andrea Nicola Saporito, Giovanna Vitaliti, Piero Pavone, et al.
European Journal of Medical Genetics|May 27, 2020
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2Piero Pavone, Xena Giada Pappalardo, Gemma Incorpora, et al.
Translational Pediatrics|March 9, 2023
Impressive efficacy of the ketogenic diet in a KCNQ2 encephalopathy infant: a case report and exhaustive literature reviewRaffaele Falsaperla, Simona Domenica Marino, Giulia Salomone, et al.
Italian Journal of Pediatrics|December 5, 2024
Cranial ultrasonographic findings in newborns exposed to SARS-CoV-2: a single-centre cross-sectional analysisBruna Scalia, Marco Andrea Nicola Saporito, Laura Mauceri, et al.
Pageof 26

Showing results (151-160 of 251) with videos related to

Sort By:
Pageof 26
Journal of Pediatric Genetics|July 28, 2020
Primary Microcephaly with Novel Variant of <i>MCPH1</i> Gene in Twins: Both Manifesting in Childhood at the Same Time with Hashimoto's ThyroiditisPiero Pavone, Xena Giada Pappalardo, Andrea Domenico Praticò, et al.
Frontiers in Pediatrics|October 12, 2020
Intronic Variant in <i>CNTNAP2</i> Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and SeizuresRaffaele Falsaperla, Xena Giada Pappalardo, Catia Romano, et al.
Children (Basel, Switzerland)|September 28, 2021
The Evolution of the Role of Imaging in the Diagnosis of Craniosynostosis: A Narrative ReviewGiovanni Cacciaguerra, Monica Palermo, Lidia Marino, et al.
Clinical and Experimental Vaccine Research|August 15, 2024
SARS-CoV-2 parental vaccination and risk of multisystem inflammatory syndrome in children: a single-center retrospective studyRaffaele Falsaperla, Vincenzo Sortino, Ausilia Desiree Collotta, et al.
Children (Basel, Switzerland)|May 27, 2023
SARS-CoV-2 and Swabs: Disease Severity and the Numbers of Cycles of Gene Amplification, Single Center ExperienceRaffaele Falsaperla, Vincenzo Sortino, Ausilia Desiree Collotta, et al.
World Neurosurgery|June 6, 2022
Decision-Making Challenge of Ping-Pong Fractures in Children: Case Exemplification and Systematic Review of LiteratureRoberto Altieri, Erica Grasso, Giacomo Cammarata, et al.
Neuropsychiatric Disease and Treatment|June 16, 2017
Ictal blinking, an under-recognized phenomenon: our experience and literature reviewMarco Andrea Nicola Saporito, Giovanna Vitaliti, Piero Pavone, et al.
European Journal of Medical Genetics|May 27, 2020
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2Piero Pavone, Xena Giada Pappalardo, Gemma Incorpora, et al.
Translational Pediatrics|March 9, 2023
Impressive efficacy of the ketogenic diet in a KCNQ2 encephalopathy infant: a case report and exhaustive literature reviewRaffaele Falsaperla, Simona Domenica Marino, Giulia Salomone, et al.
Italian Journal of Pediatrics|December 5, 2024
Cranial ultrasonographic findings in newborns exposed to SARS-CoV-2: a single-centre cross-sectional analysisBruna Scalia, Marco Andrea Nicola Saporito, Laura Mauceri, et al.
Pageof 26