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

Renzo Guerrini

Showing results (141-150 of 610) with videos related to

Pageof 61
Sort By:
Neurology|September 6, 2019
Subcortical heterotopic gray matter brain malformations: Classification study of 107 individualsRenske Oegema, A James Barkovich, Grazia M S Mancini, et al.
Epilepsy & Behavior : E&B|January 9, 2015
A novel inherited SCN1A mutation associated with different neuropsychological phenotypes: is there a common core deficit?Claudia Passamonti, Cristina Petrelli, Davide Mei, et al.
Therapeutic Drug Monitoring|November 26, 2003
Influence of dosage, age, and co-medication on plasma topiramate concentrations in children and adults with severe epilepsy and preliminary observations on correlations with clinical responseAnna Rita Ferrari, Renzo Guerrini, Giuliana Gatti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 15, 2015
Mitochondrial respiratory chain defects in skin fibroblasts from patients with Dravet syndromeStefano Doccini, Maria Chiara Meschini, Davide Mei, et al.
Brain : a Journal of Neurology|March 20, 2012
A developmental and genetic classification for malformations of cortical development: update 2012A James Barkovich, Renzo Guerrini, Ruben I Kuzniecky, et al.
Clinical Chemistry and Laboratory Medicine|February 3, 2025
Inclusion of pyridoxine dependent epilepsy in expanded newborn screening programs by tandem mass spectrometry: set up of first and second tier testsRoberta Damiano, Maria Della Bona, Elena Procopio, et al.
Epilepsia|January 7, 2020
Dravet syndrome: Treatment options and management of prolonged seizuresJ Helen Cross, Roberto H Caraballo, Rima Nabbout, et al.
Joint Bone Spine|December 31, 2016
Mycophenolate mofetil as induction and long-term maintaining treatment in childhood: Primary angiitis of the central nervous systemAnna Rosati, Alessandra Cosi, Massimo Basile, et al.
Journal of Neurology|November 2, 2018
Progressive myoclonus epilepsy in Gaucher Disease due to a new Gly-Gly mutation causing loss of an Exonic Splicing EnhancerRodolfo Tonin, Serena Catarzi, Anna Caciotti, et al.
Rapid Communications in Mass Spectrometry : RCM|November 11, 2009
The successful inclusion of succinylacetone as a marker of tyrosinemia type I in Tuscany newborn screening programGiancarlo la Marca, Sabrina Malvagia, Silvia Funghini, et al.
Pageof 61

Showing results (141-150 of 610) with videos related to

Sort By:
Pageof 61
Neurology|September 6, 2019
Subcortical heterotopic gray matter brain malformations: Classification study of 107 individualsRenske Oegema, A James Barkovich, Grazia M S Mancini, et al.
Epilepsy & Behavior : E&B|January 9, 2015
A novel inherited SCN1A mutation associated with different neuropsychological phenotypes: is there a common core deficit?Claudia Passamonti, Cristina Petrelli, Davide Mei, et al.
Therapeutic Drug Monitoring|November 26, 2003
Influence of dosage, age, and co-medication on plasma topiramate concentrations in children and adults with severe epilepsy and preliminary observations on correlations with clinical responseAnna Rita Ferrari, Renzo Guerrini, Giuliana Gatti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 15, 2015
Mitochondrial respiratory chain defects in skin fibroblasts from patients with Dravet syndromeStefano Doccini, Maria Chiara Meschini, Davide Mei, et al.
Brain : a Journal of Neurology|March 20, 2012
A developmental and genetic classification for malformations of cortical development: update 2012A James Barkovich, Renzo Guerrini, Ruben I Kuzniecky, et al.
Clinical Chemistry and Laboratory Medicine|February 3, 2025
Inclusion of pyridoxine dependent epilepsy in expanded newborn screening programs by tandem mass spectrometry: set up of first and second tier testsRoberta Damiano, Maria Della Bona, Elena Procopio, et al.
Epilepsia|January 7, 2020
Dravet syndrome: Treatment options and management of prolonged seizuresJ Helen Cross, Roberto H Caraballo, Rima Nabbout, et al.
Joint Bone Spine|December 31, 2016
Mycophenolate mofetil as induction and long-term maintaining treatment in childhood: Primary angiitis of the central nervous systemAnna Rosati, Alessandra Cosi, Massimo Basile, et al.
Journal of Neurology|November 2, 2018
Progressive myoclonus epilepsy in Gaucher Disease due to a new Gly-Gly mutation causing loss of an Exonic Splicing EnhancerRodolfo Tonin, Serena Catarzi, Anna Caciotti, et al.
Rapid Communications in Mass Spectrometry : RCM|November 11, 2009
The successful inclusion of succinylacetone as a marker of tyrosinemia type I in Tuscany newborn screening programGiancarlo la Marca, Sabrina Malvagia, Silvia Funghini, et al.
Pageof 61