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

Aurore Curie

Showing results (1-10 of 31) with videos related to

Pageof 4
Sort By:
La Revue Du Praticien|March 16, 2010
[Problems posed by genetic diseases, concerning DNA instability disorders: fragile X syndrome]Gaëtan Lesca, Aurore Curie, Christophe Rousselle
Developmental Medicine and Child Neurology|March 14, 2023
Placebo effects in children with autism spectrum disorderAurore Curie, Tim F Oberlander, Karin B Jensen
Experimental Brain Research|April 26, 2013
Simultaneous action execution and observation optimise grasping actionsMathilde Ménoret, Aurore Curie, Vincent des Portes, et al.
Frontiers in Human Neuroscience|October 18, 2013
Motor resonance facilitates movement execution: an ERP and kinematic studyMathilde Ménoret, Aurore Curie, Vincent des Portes, et al.
Presse Medicale (Paris, France : 1983)|January 4, 2015
[Transient ischemic attack: as well a paediatric emergency]Anna Hubert, Aurore Curie, Isabelle Sabatier, et al.
The Journal of Pediatrics|August 28, 2007
Long-term follow-up in 12 children with pulmonary arteriovenous malformations: confirmation of hereditary hemorrhagic telangiectasia in all casesAurore Curie, Gaëtan Lesca, Vincent Cottin, et al.
Plos One|August 31, 2013
Syntax at hand: common syntactic structures for actions and languageAlice C Roy, Aurore Curie, Tatjana Nazir, et al.
Plos One|July 31, 2015
Placebo Responses in Genetically Determined Intellectual Disability: A Meta-AnalysisAurore Curie, Kathy Yang, Irving Kirsch, et al.
Neuropsychologia|October 26, 2013
Neural correlates of non-verbal social interactions: a dual-EEG studyMathilde Ménoret, Léo Varnet, Raphaël Fargier, et al.
Developmental Medicine and Child Neurology|August 15, 2019
Expanding the phenotypic spectrum of Allan-Herndon-Dudley syndrome in patients with SLC16A2 mutationsGanaelle Remerand, Odile Boespflug-Tanguy, Davide Tonduti, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
La Revue Du Praticien|March 16, 2010
[Problems posed by genetic diseases, concerning DNA instability disorders: fragile X syndrome]Gaëtan Lesca, Aurore Curie, Christophe Rousselle
Developmental Medicine and Child Neurology|March 14, 2023
Placebo effects in children with autism spectrum disorderAurore Curie, Tim F Oberlander, Karin B Jensen
Experimental Brain Research|April 26, 2013
Simultaneous action execution and observation optimise grasping actionsMathilde Ménoret, Aurore Curie, Vincent des Portes, et al.
Frontiers in Human Neuroscience|October 18, 2013
Motor resonance facilitates movement execution: an ERP and kinematic studyMathilde Ménoret, Aurore Curie, Vincent des Portes, et al.
Presse Medicale (Paris, France : 1983)|January 4, 2015
[Transient ischemic attack: as well a paediatric emergency]Anna Hubert, Aurore Curie, Isabelle Sabatier, et al.
The Journal of Pediatrics|August 28, 2007
Long-term follow-up in 12 children with pulmonary arteriovenous malformations: confirmation of hereditary hemorrhagic telangiectasia in all casesAurore Curie, Gaëtan Lesca, Vincent Cottin, et al.
Plos One|August 31, 2013
Syntax at hand: common syntactic structures for actions and languageAlice C Roy, Aurore Curie, Tatjana Nazir, et al.
Plos One|July 31, 2015
Placebo Responses in Genetically Determined Intellectual Disability: A Meta-AnalysisAurore Curie, Kathy Yang, Irving Kirsch, et al.
Neuropsychologia|October 26, 2013
Neural correlates of non-verbal social interactions: a dual-EEG studyMathilde Ménoret, Léo Varnet, Raphaël Fargier, et al.
Developmental Medicine and Child Neurology|August 15, 2019
Expanding the phenotypic spectrum of Allan-Herndon-Dudley syndrome in patients with SLC16A2 mutationsGanaelle Remerand, Odile Boespflug-Tanguy, Davide Tonduti, et al.
Pageof 4