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Oriane Trouillard

Showing results (21-30 of 36) with videos related to

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Journal of Medical Genetics|June 5, 2010
Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndromeChristel Depienne, Oriane Trouillard, Isabelle Gourfinkel-An, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|December 12, 2019
Association of Rare Genetic Variants in Opioid Receptors with Tourette SyndromeChristel Depienne, Sorana Ciura, Oriane Trouillard, et al.
Human Brain Mapping|January 18, 2019
The supplementary motor area modulates interhemispheric interactions during movement preparationQuentin Welniarz, Cécile Gallea, Jean-Charles Lamy, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|July 17, 2023
Correction: Association of Rare Genetic Variants in Opioid Receptors with Tourette SyndromeChristel Depienne, Sorana Ciura, Oriane Trouillard, et al.
Movement Disorders Clinical Practice|June 12, 2025
ADCY5-Mosaic Variants: A Diagnosis Not to Be MissedAlice Innocenti, Emmanuel Roze, Florence Riant, et al.
Biological Psychiatry|March 13, 2009
Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disordersChristel Depienne, Daniel Moreno-De-Luca, Delphine Heron, 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.
Plos Genetics|February 14, 2009
Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects femalesChristel Depienne, Delphine Bouteiller, Boris Keren, et al.
Human Mutation|November 6, 2010
Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in femalesChristel Depienne, Oriane Trouillard, Delphine Bouteiller, 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.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Journal of Medical Genetics|June 5, 2010
Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndromeChristel Depienne, Oriane Trouillard, Isabelle Gourfinkel-An, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|December 12, 2019
Association of Rare Genetic Variants in Opioid Receptors with Tourette SyndromeChristel Depienne, Sorana Ciura, Oriane Trouillard, et al.
Human Brain Mapping|January 18, 2019
The supplementary motor area modulates interhemispheric interactions during movement preparationQuentin Welniarz, Cécile Gallea, Jean-Charles Lamy, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|July 17, 2023
Correction: Association of Rare Genetic Variants in Opioid Receptors with Tourette SyndromeChristel Depienne, Sorana Ciura, Oriane Trouillard, et al.
Movement Disorders Clinical Practice|June 12, 2025
ADCY5-Mosaic Variants: A Diagnosis Not to Be MissedAlice Innocenti, Emmanuel Roze, Florence Riant, et al.
Biological Psychiatry|March 13, 2009
Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disordersChristel Depienne, Daniel Moreno-De-Luca, Delphine Heron, 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.
Plos Genetics|February 14, 2009
Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects femalesChristel Depienne, Delphine Bouteiller, Boris Keren, et al.
Human Mutation|November 6, 2010
Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in femalesChristel Depienne, Oriane Trouillard, Delphine Bouteiller, 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.
Pageof 4