Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Carlo Fusco

Showing results (51-60 of 148) with videos related to

Pageof 15
Sort By:
Plos One|May 26, 2011
Identification of prognostic molecular features in the reactive stroma of human breast and prostate cancerAnne Planche, Marina Bacac, Paolo Provero, et al.
Brain & Development|July 24, 2010
Cerebellar atrophy in a child with hereditary methemoglobinemia type IICarlo Fusco, Giuliana Soncini, Daniele Frattini, et al.
Italian Journal of Pediatrics|November 28, 2023
Tolosa-Hunt syndrome and recurrent painful ophthalmoplegic neuropathy, case reports: what to do and when?Daniele Frattini, Alessandro Iodice, Carlotta Spagnoli, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 2, 2015
CMV-associated axonal sensory-motor Guillain-Barré syndrome in a child: Case report and review of the literatureCarlotta Spagnoli, Alessandro Iodice, Grazia Gabriella Salerno, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 16, 2016
Expanding phenotype of PRRT2 gene mutations: A new case with epilepsy and benign myoclonus of early infancyIlenia Maini, Alessandro Iodice, Carlotta Spagnoli, et al.
Movement Disorders Clinical Practice|January 9, 2026
The Criss-Cross Gait Is Not Child's PlaySusanna Rizzi, Carlo Alberto Cesaroni, Daniele Frattini, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|October 5, 2021
Beneficial effects of the ketogenic diet on drug-resistant epileptic encephalopathy associated with a de novo NBEA pathogenic variantSilvia Schiavoni, Carlotta Spagnoli, Susanna Rizzi, et al.
Cerebellum (London, England)|November 14, 2020
Infantile-Onset Spinocerebellar Ataxia Type 5 (SCA5) with Optic Atrophy and Peripheral NeuropathyCarlotta Spagnoli, Daniele Frattini, Fabrizio Gozzi, et al.
Developmental Medicine and Child Neurology|April 12, 2020
Paediatric-onset hereditary spastic paraplegias: a retrospective cohort studySilvia Schiavoni, Carlotta Spagnoli, Susanna Rizzi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 28, 2021
Growth hormone deficiency in a child with benign hereditary chorea caused by a <i>de novo</i> mutation of the TITF1/NKX2-1 geneViola Trevisani, Barbara Predieri, Simona Filomena Madeo, et al.
Pageof 15

Showing results (51-60 of 148) with videos related to

Sort By:
Pageof 15
Plos One|May 26, 2011
Identification of prognostic molecular features in the reactive stroma of human breast and prostate cancerAnne Planche, Marina Bacac, Paolo Provero, et al.
Brain & Development|July 24, 2010
Cerebellar atrophy in a child with hereditary methemoglobinemia type IICarlo Fusco, Giuliana Soncini, Daniele Frattini, et al.
Italian Journal of Pediatrics|November 28, 2023
Tolosa-Hunt syndrome and recurrent painful ophthalmoplegic neuropathy, case reports: what to do and when?Daniele Frattini, Alessandro Iodice, Carlotta Spagnoli, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 2, 2015
CMV-associated axonal sensory-motor Guillain-Barré syndrome in a child: Case report and review of the literatureCarlotta Spagnoli, Alessandro Iodice, Grazia Gabriella Salerno, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 16, 2016
Expanding phenotype of PRRT2 gene mutations: A new case with epilepsy and benign myoclonus of early infancyIlenia Maini, Alessandro Iodice, Carlotta Spagnoli, et al.
Movement Disorders Clinical Practice|January 9, 2026
The Criss-Cross Gait Is Not Child's PlaySusanna Rizzi, Carlo Alberto Cesaroni, Daniele Frattini, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|October 5, 2021
Beneficial effects of the ketogenic diet on drug-resistant epileptic encephalopathy associated with a de novo NBEA pathogenic variantSilvia Schiavoni, Carlotta Spagnoli, Susanna Rizzi, et al.
Cerebellum (London, England)|November 14, 2020
Infantile-Onset Spinocerebellar Ataxia Type 5 (SCA5) with Optic Atrophy and Peripheral NeuropathyCarlotta Spagnoli, Daniele Frattini, Fabrizio Gozzi, et al.
Developmental Medicine and Child Neurology|April 12, 2020
Paediatric-onset hereditary spastic paraplegias: a retrospective cohort studySilvia Schiavoni, Carlotta Spagnoli, Susanna Rizzi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 28, 2021
Growth hormone deficiency in a child with benign hereditary chorea caused by a <i>de novo</i> mutation of the TITF1/NKX2-1 geneViola Trevisani, Barbara Predieri, Simona Filomena Madeo, et al.
Pageof 15