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

Caroline Demily

Showing results (51-60 of 80) with videos related to

Pageof 8
Sort By:
Annals of General Psychiatry|April 11, 2017
Screening of Wilson's disease in a psychiatric population: difficulties and pitfalls. A preliminary studyCaroline Demily, François Parant, David Cheillan, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 9, 2008
No pathogenic rearrangement within the DISC 1 gene in psychosisSolenn Legallic, Jacqueline Bou, Sadeq Haouzir, et al.
BMC Medical Genetics|February 1, 2017
Autism spectrum disorder associated with 49,XYYYY: case report and review of the literatureCaroline Demily, Alice Poisson, Elodie Peyroux, et al.
BMC Medical Genetics|January 10, 2020
Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case reportAlice Poisson, Nicolas Chatron, Audrey Labalme, et al.
Children (Basel, Switzerland)|November 27, 2025
Clinical, Sleep, and Chronobiological Characteristics of Children with Smith-Magenis Syndrome Under Treatment for Sleep DisordersMarion Comajuan, Aurore Guyon, Véronique Raverot, et al.
European Child & Adolescent Psychiatry|July 8, 2015
Facial emotion perception by intensity in children and adolescents with 22q11.2 deletion syndromeArnaud Leleu, Guillaume Saucourt, Caroline Rigard, et al.
BMC Psychiatry|July 18, 2021
Erotomania and phenotypic continuum in a family frameshift variant of AUTS2: a case report and reviewChristophe Gauld, Alice Poisson, Julie Reversat, et al.
Translational Psychiatry|February 6, 2019
An implicit and reliable neural measure quantifying impaired visual coding of facial expression: evidence from the 22q11.2 deletion syndromeArnaud Leleu, Emilie Favre, Alexandre Yailian, et al.
Plos One|April 7, 2017
Social cognition in Wilson's disease: A new phenotype?Elodie Peyroux, Nelly Santaella, Emmanuel Broussolle, et al.
Psychiatry Research|November 10, 2016
Does COMT val158met polymorphism influence P50 sensory gating, eye tracking or saccadic inhibition dysfunctions in schizophrenia?Caroline Demily, Sandrine Louchart-de-la-Chapelle, Irène Nkam, et al.
Pageof 8

Showing results (51-60 of 80) with videos related to

Sort By:
Pageof 8
Annals of General Psychiatry|April 11, 2017
Screening of Wilson's disease in a psychiatric population: difficulties and pitfalls. A preliminary studyCaroline Demily, François Parant, David Cheillan, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 9, 2008
No pathogenic rearrangement within the DISC 1 gene in psychosisSolenn Legallic, Jacqueline Bou, Sadeq Haouzir, et al.
BMC Medical Genetics|February 1, 2017
Autism spectrum disorder associated with 49,XYYYY: case report and review of the literatureCaroline Demily, Alice Poisson, Elodie Peyroux, et al.
BMC Medical Genetics|January 10, 2020
Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case reportAlice Poisson, Nicolas Chatron, Audrey Labalme, et al.
Children (Basel, Switzerland)|November 27, 2025
Clinical, Sleep, and Chronobiological Characteristics of Children with Smith-Magenis Syndrome Under Treatment for Sleep DisordersMarion Comajuan, Aurore Guyon, Véronique Raverot, et al.
European Child & Adolescent Psychiatry|July 8, 2015
Facial emotion perception by intensity in children and adolescents with 22q11.2 deletion syndromeArnaud Leleu, Guillaume Saucourt, Caroline Rigard, et al.
BMC Psychiatry|July 18, 2021
Erotomania and phenotypic continuum in a family frameshift variant of AUTS2: a case report and reviewChristophe Gauld, Alice Poisson, Julie Reversat, et al.
Translational Psychiatry|February 6, 2019
An implicit and reliable neural measure quantifying impaired visual coding of facial expression: evidence from the 22q11.2 deletion syndromeArnaud Leleu, Emilie Favre, Alexandre Yailian, et al.
Plos One|April 7, 2017
Social cognition in Wilson's disease: A new phenotype?Elodie Peyroux, Nelly Santaella, Emmanuel Broussolle, et al.
Psychiatry Research|November 10, 2016
Does COMT val158met polymorphism influence P50 sensory gating, eye tracking or saccadic inhibition dysfunctions in schizophrenia?Caroline Demily, Sandrine Louchart-de-la-Chapelle, Irène Nkam, et al.
Pageof 8