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Oriane Trouillard

Showing results (11-20 of 36) with videos related to

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Tremor and Other Hyperkinetic Movements (New York, N.Y.)|November 11, 2016
Congenital Mirror Movements Due to RAD51: Cosegregation with a Nonsense Mutation in a Norwegian Pedigree and Review of the LiteratureOriane Trouillard, Jeanette Koht, Thorsten Gerstner, et al.
Human Mutation|March 17, 2006
Parental mosaicism can cause recurrent transmission of SCN1A mutations associated with severe myoclonic epilepsy of infancyChristel Depienne, Alexis Arzimanoglou, Oriane Trouillard, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 21, 2011
Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolismPhilippe Couarch, Santiago Vernia, Isabelle Gourfinkel-An, et al.
Epilepsy Research|September 8, 2009
CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancyRima Nabbout, Christel Depienne, Mathilde Chipaux, et al.
Epilepsia|July 19, 2011
STXBP1-related encephalopathy presenting as infantile spasms and generalized tremor in three patientsCyril Mignot, Marie-Laure Moutard, Oriane Trouillard, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 26, 2021
SCN1A-related epilepsy with recessive inheritance: Two further familiesRaffaella Moretti, Lionel Arnaud, Delphine Bouteiller, et al.
Epilepsy Research|August 8, 2007
Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsyElodie Chabrol, Isabelle Gourfinkel-An, Ingrid E Scheffer, et al.
Scientific Reports|March 26, 2017
Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midlineQuentin Welniarz, Marie-Pierre Morel, Oriane Pourchet, et al.
Journal of Medical Genetics|June 12, 2023
Congenital mirror movements are associated with defective polymerisation of RAD51Oriane Trouillard, Pauline Dupaigne, Margaux Dunoyer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 4, 2024
Rare Missense Variants in KCNJ10 Are Associated with Paroxysmal Kinesigenic DyskinesiaThomas Wirth, Emmanuel Roze, Clarisse Delvallée, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|November 11, 2016
Congenital Mirror Movements Due to RAD51: Cosegregation with a Nonsense Mutation in a Norwegian Pedigree and Review of the LiteratureOriane Trouillard, Jeanette Koht, Thorsten Gerstner, et al.
Human Mutation|March 17, 2006
Parental mosaicism can cause recurrent transmission of SCN1A mutations associated with severe myoclonic epilepsy of infancyChristel Depienne, Alexis Arzimanoglou, Oriane Trouillard, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 21, 2011
Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolismPhilippe Couarch, Santiago Vernia, Isabelle Gourfinkel-An, et al.
Epilepsy Research|September 8, 2009
CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancyRima Nabbout, Christel Depienne, Mathilde Chipaux, et al.
Epilepsia|July 19, 2011
STXBP1-related encephalopathy presenting as infantile spasms and generalized tremor in three patientsCyril Mignot, Marie-Laure Moutard, Oriane Trouillard, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 26, 2021
SCN1A-related epilepsy with recessive inheritance: Two further familiesRaffaella Moretti, Lionel Arnaud, Delphine Bouteiller, et al.
Epilepsy Research|August 8, 2007
Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsyElodie Chabrol, Isabelle Gourfinkel-An, Ingrid E Scheffer, et al.
Scientific Reports|March 26, 2017
Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midlineQuentin Welniarz, Marie-Pierre Morel, Oriane Pourchet, et al.
Journal of Medical Genetics|June 12, 2023
Congenital mirror movements are associated with defective polymerisation of RAD51Oriane Trouillard, Pauline Dupaigne, Margaux Dunoyer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 4, 2024
Rare Missense Variants in KCNJ10 Are Associated with Paroxysmal Kinesigenic DyskinesiaThomas Wirth, Emmanuel Roze, Clarisse Delvallée, et al.
Pageof 4