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Raffaele Falsaperla

Showing results (61-70 of 251) with videos related to

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American Journal of Medical Genetics. Part A|January 31, 2014
Klippel-Trenaunay syndrome in a boy with concomitant ipsilateral overgrowth and undergrowthMartino Ruggieri, Vito Pavone, Agata Polizzi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 20, 2023
Is ketogenic diet a 'precision medicine'? Recent developments and future challengesRaffaele Falsaperla, Vincenzo Sortino, Pasquale Striano, et al.
Case Reports in Pediatrics|October 16, 2020
Diagnostic Clue in a Neonate with Amniotic Band SequenceRaffaele Falsaperla, Marta Arrabito, Piero Pavone, et al.
Italian Journal of Pediatrics|May 17, 2018
Benign and severe early-life seizures: a round in the first year of lifePiero Pavone, Giovanni Corsello, Martino Ruggieri, et al.
Acta Bio-Medica : Atenei Parmensis|September 14, 2020
Celiac disease and headache in children: a narrative state of the artLuca Sabino, Silvia Marino, Raffaele Falsaperla, et al.
Journal of Pediatric Neurosciences|September 15, 2017
Pediatric Autoimmune EncephalitisMassimo Barbagallo, Giovanna Vitaliti, Piero Pavone, et al.
Journal of Pediatric Genetics|December 2, 2021
A Novel 4q32.3 Deletion in a Child: Additional Signs and the Role of <i>MARCH1</i>Xena Giada Pappalardo, Martino Ruggieri, Raffaele Falsaperla, et al.
Clinical Neurology and Neurosurgery|April 14, 2012
Spine and brain malformations in a patient obligate carrier of MTHFR with autism and mental retardationVito Pavone, Andrea Domenico Praticò, Enrico Parano, et al.
Italian Journal of Pediatrics|June 6, 2022
Diagnostic controversies in recurrent painful ophthalmoplegic neuropathy: single case report with a systematic reviewRaffaele Falsaperla, Santiago Presti, Manuela Lo Bianco, et al.
Frontiers in Pediatrics|April 17, 2023
Case report: A gain-of-function of hamartin may lead to a distinct "inverse <i>TSC1</i>-hamartin" phenotype characterized by reduced cell growthAndrea D Praticò, Raffaele Falsaperla, Mattia Comella, et al.
Pageof 26

Showing results (61-70 of 251) with videos related to

Sort By:
Pageof 26
American Journal of Medical Genetics. Part A|January 31, 2014
Klippel-Trenaunay syndrome in a boy with concomitant ipsilateral overgrowth and undergrowthMartino Ruggieri, Vito Pavone, Agata Polizzi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 20, 2023
Is ketogenic diet a 'precision medicine'? Recent developments and future challengesRaffaele Falsaperla, Vincenzo Sortino, Pasquale Striano, et al.
Case Reports in Pediatrics|October 16, 2020
Diagnostic Clue in a Neonate with Amniotic Band SequenceRaffaele Falsaperla, Marta Arrabito, Piero Pavone, et al.
Italian Journal of Pediatrics|May 17, 2018
Benign and severe early-life seizures: a round in the first year of lifePiero Pavone, Giovanni Corsello, Martino Ruggieri, et al.
Acta Bio-Medica : Atenei Parmensis|September 14, 2020
Celiac disease and headache in children: a narrative state of the artLuca Sabino, Silvia Marino, Raffaele Falsaperla, et al.
Journal of Pediatric Neurosciences|September 15, 2017
Pediatric Autoimmune EncephalitisMassimo Barbagallo, Giovanna Vitaliti, Piero Pavone, et al.
Journal of Pediatric Genetics|December 2, 2021
A Novel 4q32.3 Deletion in a Child: Additional Signs and the Role of <i>MARCH1</i>Xena Giada Pappalardo, Martino Ruggieri, Raffaele Falsaperla, et al.
Clinical Neurology and Neurosurgery|April 14, 2012
Spine and brain malformations in a patient obligate carrier of MTHFR with autism and mental retardationVito Pavone, Andrea Domenico Praticò, Enrico Parano, et al.
Italian Journal of Pediatrics|June 6, 2022
Diagnostic controversies in recurrent painful ophthalmoplegic neuropathy: single case report with a systematic reviewRaffaele Falsaperla, Santiago Presti, Manuela Lo Bianco, et al.
Frontiers in Pediatrics|April 17, 2023
Case report: A gain-of-function of hamartin may lead to a distinct "inverse <i>TSC1</i>-hamartin" phenotype characterized by reduced cell growthAndrea D Praticò, Raffaele Falsaperla, Mattia Comella, et al.
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