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Oriane Trouillard

Showing results (1-10 of 36) with videos related to

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Developmental Medicine and Child Neurology|May 27, 2015
Congenital mirror movements caused by a mutation in the DCC geneAurelie Meneret, Oriane Trouillard, Vanessa Brochard, et al.
Neurology|February 26, 2015
Congenital mirror movements: from piano player to opera singerAurélie Méneret, Quentin Welniarz, Oriane Trouillard, et al.
Journal of Neurology|September 20, 2014
Congenital mirror movements: no mutation in DNAL4 in 17 index casesAurélie Méneret, Oriane Trouillard, Marie Vidailhet, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 7, 2025
Comment on Schwarz et al. "EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder"Oriane Trouillard, Quentin Welniarz, Aurélie Méneret, et al.
Pediatric Neurology|September 15, 2023
Mirror Movements Due To a TUBB3 VariantClément Desjardins, Domitille Gras, Oriane Trouillard, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 17, 2024
Comment on "Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals"Oriane Trouillard, Aurélie Méneret, Margaux Dunoyer, et al.
American Journal of Medical Genetics. Part A|November 9, 2011
Intragenic deletion of UBE3A gene in 2 sisters with Angelman syndrome detected by MLPAJuliette Piard, Christel Depienne, Boris Keren, et al.
Cancer Genetics and Cytogenetics|June 3, 2004
Parental 19q loss and PEG3 expression in oligodendrogliomasOriane Trouillard, Lucinda Aguirre-Cruz, Khe Hoang-Xuan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 22, 2015
ADCY5 mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesiasJennifer R Friedman, Aurélie Méneret, Dong-Hui Chen, et al.
Archives of Neurology|February 14, 2007
Two novel epilepsy-linked mutations leading to a loss of function of LGI1Elodie Chabrol, Cyprian Popescu, Isabelle Gourfinkel-An, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Developmental Medicine and Child Neurology|May 27, 2015
Congenital mirror movements caused by a mutation in the DCC geneAurelie Meneret, Oriane Trouillard, Vanessa Brochard, et al.
Neurology|February 26, 2015
Congenital mirror movements: from piano player to opera singerAurélie Méneret, Quentin Welniarz, Oriane Trouillard, et al.
Journal of Neurology|September 20, 2014
Congenital mirror movements: no mutation in DNAL4 in 17 index casesAurélie Méneret, Oriane Trouillard, Marie Vidailhet, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 7, 2025
Comment on Schwarz et al. "EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder"Oriane Trouillard, Quentin Welniarz, Aurélie Méneret, et al.
Pediatric Neurology|September 15, 2023
Mirror Movements Due To a TUBB3 VariantClément Desjardins, Domitille Gras, Oriane Trouillard, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 17, 2024
Comment on "Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals"Oriane Trouillard, Aurélie Méneret, Margaux Dunoyer, et al.
American Journal of Medical Genetics. Part A|November 9, 2011
Intragenic deletion of UBE3A gene in 2 sisters with Angelman syndrome detected by MLPAJuliette Piard, Christel Depienne, Boris Keren, et al.
Cancer Genetics and Cytogenetics|June 3, 2004
Parental 19q loss and PEG3 expression in oligodendrogliomasOriane Trouillard, Lucinda Aguirre-Cruz, Khe Hoang-Xuan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 22, 2015
ADCY5 mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesiasJennifer R Friedman, Aurélie Méneret, Dong-Hui Chen, et al.
Archives of Neurology|February 14, 2007
Two novel epilepsy-linked mutations leading to a loss of function of LGI1Elodie Chabrol, Cyprian Popescu, Isabelle Gourfinkel-An, et al.
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