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

Florence Riant

Showing results (51-60 of 68) with videos related to

Pageof 7
Sort By:
Neurology|January 21, 2022
Cerebellum Dysfunction in Patients With <i>PRRT2</i>-Related Paroxysmal DyskinesiaAsya Ekmen, Aurelie Meneret, Romain Valabregue, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 31, 2026
Psychiatric Disorders and Apathy in Mixed Movement Disorders Linked to ADCY5 (MxMD-ADCY5)Aurélie Méneret, Clément Tarrano, Asya Ekmen, et al.
Journal of Alzheimer'S Disease : JAD|November 19, 2016
APP Mutations in Cerebral Amyloid Angiopathy with or without Cortical Calcifications: Report of Three Families and a Literature ReviewFrançois Sellal, David Wallon, Laurent Martinez-Almoyna, et al.
European Journal of Human Genetics : EJHG|April 2, 2015
Mutation in the 3'untranslated region of APP as a genetic determinant of cerebral amyloid angiopathyGaël Nicolas, David Wallon, Claudia Goupil, et al.
Brain Communications|November 11, 2025
Clinical and molecular landscape of paediatric cerebral and spinal cavernous malformationsSandro Benichi, Estelle Balducci, Joseph Benzakoun, et al.
Brain : a Journal of Neurology|April 27, 2017
A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathiesMarie Coutelier, Giulia Coarelli, Marie-Lorraine Monin, et al.
The Journal of Clinical Investigation|September 26, 2017
Mutations in the netrin-1 gene cause congenital mirror movementsAurélie Méneret, Elizabeth A Franz, Oriane Trouillard, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 8, 2021
CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patientsMarie Le Roux, Magalie Barth, Sophie Gueden, et al.
Neurology|October 15, 2021
Hemiplegic Migraine Associated With <i>PRRT2</i> Variations: A Clinical and Genetic StudyFlorence Riant, Caroline Roos, Agathe Roubertie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 13, 2018
Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathiesStéphanie Valence, Emmanuelle Cochet, Christelle Rougeot, et al.
Pageof 7

Showing results (51-60 of 68) with videos related to

Sort By:
Pageof 7
Neurology|January 21, 2022
Cerebellum Dysfunction in Patients With <i>PRRT2</i>-Related Paroxysmal DyskinesiaAsya Ekmen, Aurelie Meneret, Romain Valabregue, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 31, 2026
Psychiatric Disorders and Apathy in Mixed Movement Disorders Linked to ADCY5 (MxMD-ADCY5)Aurélie Méneret, Clément Tarrano, Asya Ekmen, et al.
Journal of Alzheimer'S Disease : JAD|November 19, 2016
APP Mutations in Cerebral Amyloid Angiopathy with or without Cortical Calcifications: Report of Three Families and a Literature ReviewFrançois Sellal, David Wallon, Laurent Martinez-Almoyna, et al.
European Journal of Human Genetics : EJHG|April 2, 2015
Mutation in the 3'untranslated region of APP as a genetic determinant of cerebral amyloid angiopathyGaël Nicolas, David Wallon, Claudia Goupil, et al.
Brain Communications|November 11, 2025
Clinical and molecular landscape of paediatric cerebral and spinal cavernous malformationsSandro Benichi, Estelle Balducci, Joseph Benzakoun, et al.
Brain : a Journal of Neurology|April 27, 2017
A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathiesMarie Coutelier, Giulia Coarelli, Marie-Lorraine Monin, et al.
The Journal of Clinical Investigation|September 26, 2017
Mutations in the netrin-1 gene cause congenital mirror movementsAurélie Méneret, Elizabeth A Franz, Oriane Trouillard, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 8, 2021
CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patientsMarie Le Roux, Magalie Barth, Sophie Gueden, et al.
Neurology|October 15, 2021
Hemiplegic Migraine Associated With <i>PRRT2</i> Variations: A Clinical and Genetic StudyFlorence Riant, Caroline Roos, Agathe Roubertie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 13, 2018
Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathiesStéphanie Valence, Emmanuelle Cochet, Christelle Rougeot, et al.
Pageof 7