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

Matteo Di Capua

Showing results (11-20 of 17) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 17 results.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 25, 2017
Bilateral loss of cortical SEPs predict severe MRI lesions in neonatal hypoxic ischemic encephalopathy treated with hypothermiaAgnese Suppiej, Ambra Cappellari, Giacomo Talenti, et al.
Plos Genetics|December 7, 2016
Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain PerceptionDeborah Chiabrando, Marco Castori, Maja di Rocco, et al.
Human Mutation|October 28, 2006
Biochemical and molecular characterization of 18 patients with pyridoxine-dependent epilepsy and mutations of the antiquitin (ALDH7A1) geneBarbara Plecko, Karl Paul, Eduard Paschke, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 8, 2021
Consensus protocol for EEG and amplitude-integrated EEG assessment and monitoring in neonatesRobertino Dilena, Federico Raviglione, Gaetano Cantalupo, et al.
Neonatology|February 27, 2022
Neonatal Cerebral Venous Thrombosis following Maternal SARS-CoV-2 Infection in PregnancyFrancesca Campi, Daniela Longo, Iliana Bersani, et al.
Human Mutation|August 21, 2015
A Novel Mutation in RPL10 (Ribosomal Protein L10) Causes X-Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo-Epiphyseal DysplasiaGinevra Zanni, Vera M Kalscheuer, Andreas Friedrich, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 24, 2016
Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxiaLorena Travaglini, Marta Nardella, Emanuele Bellacchio, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 25, 2017
Bilateral loss of cortical SEPs predict severe MRI lesions in neonatal hypoxic ischemic encephalopathy treated with hypothermiaAgnese Suppiej, Ambra Cappellari, Giacomo Talenti, et al.
Plos Genetics|December 7, 2016
Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain PerceptionDeborah Chiabrando, Marco Castori, Maja di Rocco, et al.
Human Mutation|October 28, 2006
Biochemical and molecular characterization of 18 patients with pyridoxine-dependent epilepsy and mutations of the antiquitin (ALDH7A1) geneBarbara Plecko, Karl Paul, Eduard Paschke, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 8, 2021
Consensus protocol for EEG and amplitude-integrated EEG assessment and monitoring in neonatesRobertino Dilena, Federico Raviglione, Gaetano Cantalupo, et al.
Neonatology|February 27, 2022
Neonatal Cerebral Venous Thrombosis following Maternal SARS-CoV-2 Infection in PregnancyFrancesca Campi, Daniela Longo, Iliana Bersani, et al.
Human Mutation|August 21, 2015
A Novel Mutation in RPL10 (Ribosomal Protein L10) Causes X-Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo-Epiphyseal DysplasiaGinevra Zanni, Vera M Kalscheuer, Andreas Friedrich, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 24, 2016
Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxiaLorena Travaglini, Marta Nardella, Emanuele Bellacchio, et al.
Pageof 2