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

R Guerrini

Showing results (271-280 of 276) with videos related to

Pageof 28
Sort By:
You have reached the last page of results.This site can display upto 276 results.
Human Molecular Genetics|April 1, 1997
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brainM E Ross, K M Allen, A K Srivastava, et al.
Annals of Neurology|February 16, 1999
Characterization of mutations in the gene doublecortin in patients with double cortex syndromeJ G Gleeson, S R Minnerath, J W Fox, et al.
Epilepsy Research|August 30, 2016
Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies-An Italian observational multicenter studyP De Liso, F Vigevano, N Specchio, et al.
Neurology|January 26, 2005
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndromeV L Sheen, A Jansen, M H Chen, et al.
Journal of Medical Genetics|January 8, 2008
Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesisB W M van Bon, D A Koolen, R Borgatti, et al.
European Journal of Neurology|October 10, 2018
Management of psychogenic non-epileptic seizures: a multidisciplinary approachS Gasparini, E Beghi, E Ferlazzo, et al.
Pageof 28

Showing results (271-280 of 276) with videos related to

Sort By:
Pageof 28
You have reached the last page of results.This site can display upto 276 results.
Human Molecular Genetics|April 1, 1997
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brainM E Ross, K M Allen, A K Srivastava, et al.
Annals of Neurology|February 16, 1999
Characterization of mutations in the gene doublecortin in patients with double cortex syndromeJ G Gleeson, S R Minnerath, J W Fox, et al.
Epilepsy Research|August 30, 2016
Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies-An Italian observational multicenter studyP De Liso, F Vigevano, N Specchio, et al.
Neurology|January 26, 2005
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndromeV L Sheen, A Jansen, M H Chen, et al.
Journal of Medical Genetics|January 8, 2008
Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesisB W M van Bon, D A Koolen, R Borgatti, et al.
European Journal of Neurology|October 10, 2018
Management of psychogenic non-epileptic seizures: a multidisciplinary approachS Gasparini, E Beghi, E Ferlazzo, et al.
Pageof 28