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Trouillard, Oriane
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1

Comment on "Defining the Genetic Landscape of Congenital Mi..:

Trouillard, Oriane ; Méneret, Aurélie ; Dunoyer, Margaux...
Movement Disorders.  39 (2024)  5 - p. 925-926 , 2024
Link: https://doi.org/10.1002/..
 
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2

Rare Missense Variants in KCNJ10 Are Associated with Paroxy..:

Wirth, Thomas ; Roze, Emmanuel ; Delvallée, Clarisse...
Movement Disorders.  39 (2024)  5 - p. 897-905 , 2024
Link: https://doi.org/10.1002/..
 
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3

Mirror Movements Due To a TUBB3 Variant:

Desjardins, Clément ; Gras, Domitille ; Trouillard, Oriane...
Pediatric Neurology.  148 (2023)  - p. 142-144 , 2023
Link: https://doi.org/10.1016/..
 
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4

SCN1A-related epilepsy with recessive inheritance: Two furt..:

Moretti, Raffaella ; Arnaud, Lionel ; Bouteiller, Delphine...
European Journal of Paediatric Neurology.  33 (2021)  - p. 121-124 , 2021
Link: https://doi.org/10.1016/..
 
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5

Association of Rare Genetic Variants in Opioid Receptors wi..:

Depienne, Christel ; Ciura, Sorana ; Trouillard, Oriane...
Tremor and Other Hyperkinetic Movements.  9 (2019)  0 - p. , 2019
Link: https://doi.org/10.5334/..
 
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6

The supplementary motor area modulates interhemispheric int..:

Welniarz, Quentin ; Gallea, Cécile ; Lamy, Jean‐Charles...
Human Brain Mapping.  40 (2019)  7 - p. 2125-2142 , 2019
Link: https://doi.org/10.1002/..
 
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7

DCCmutation update: Congenital mirror movements, isolated a..:

Marsh, Ashley P. L. ; Edwards, Timothy J. ; Galea, Charles...
Human Mutation.  39 (2017)  1 - p. 23-39 , 2017
Link: https://doi.org/10.1002/..
 
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8

Non cell-autonomous role of DCC in the guidance of the cort..:

Welniarz, Quentin ; Morel, Marie-Pierre ; Pourchet, Oriane...
Scientific Reports.  7 (2017)  1 - p. , 2017
Link: https://doi.org/10.1038/..
 
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9

Cover Image, Volume 39, Issue 1:

Marsh, Ashley P. L. ; Edwards, Timothy J. ; Galea, Charles...
Human Mutation.  39 (2017)  1 - p. i-i , 2017
Link: https://doi.org/10.1002/..
 
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10

Congenital Mirror Movements Due to RAD51: Cosegregation wit..:

Trouillard, Oriane ; Koht, Jeanette ; Gerstner, Thorsten...
Tremor and Other Hyperkinetic Movements.  6 (2016)  0 - p. 424 , 2016
Link: https://doi.org/10.5334/..
 
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11

ADCY5 mutation carriers display pleiotropic paroxysmal day ..:

Friedman, Jennifer R. ; Méneret, Aurélie ; Chen, Dong‐Hui...
Movement Disorders.  31 (2015)  1 - p. 147-148 , 2015
Link: https://doi.org/10.1002/..
 
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12

Congenital mirror movements caused by a mutation in theDCCg..:

Meneret, Aurelie ; Trouillard, Oriane ; Brochard, Vanessa.
Developmental Medicine & Child Neurology.  57 (2015)  8 - p. 776-776 , 2015
Link: https://doi.org/10.1111/..
 
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13

ADCY5-related dyskinesia: Broader spectrum and genotype–phe..:

Chen, Dong-Hui ; Méneret, Aurélie ; Friedman, Jennifer R....
Neurology.  85 (2015)  23 - p. 2026-2035 , 2015
Link: https://doi.org/10.1212/..
 
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14

Congenital mirror movements: From piano player to opera sin..:

Méneret, Aurélie ; Welniarz, Quentin ; Trouillard, Oriane.
Neurology.  84 (2015)  8 - p. 860-860 , 2015
Link: https://doi.org/10.1212/..
 
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15

Congenital mirror movements: Mutational analysis ofRAD51and..:

Méneret, Aurélie ; Depienne, Christel ; Riant, Florence...
Neurology.  82 (2014)  22 - p. 1999-2002 , 2014
Link: https://doi.org/10.1212/..
 
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