Oriane Trouillard
Overview
Explore the profile of Oriane Trouillard including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
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Articles
32
Citations
768
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0
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Recent Articles
1.
Trouillard O, Meneret A, Dunoyer M, Doulazmi M, Dusart I, Dubacq C, et al.
Mov Disord
. 2024 May;
39(5):925-926.
PMID: 38757571
No abstract available.
2.
Wirth T, Roze E, Delvallee C, Trouillard O, Drouot N, Damier P, et al.
Mov Disord
. 2024 Mar;
39(5):897-905.
PMID: 38436103
Background: Although the group of paroxysmal kinesigenic dyskinesia (PKD) genes is expanding, the molecular cause remains elusive in more than 50% of cases. Objective: The aim is to identify the...
3.
Desjardins C, Gras D, Trouillard O, Dubacq C, Boespflug Tanguy O, Roze E
Pediatr Neurol
. 2023 Sep;
148:142-144.
PMID: 37713978
No abstract available.
4.
Depienne C, Ciura S, Trouillard O, Bouteiller D, Leitao E, Nava C, et al.
Tremor Other Hyperkinet Mov (N Y)
. 2023 Jul;
13:22.
PMID: 37457636
[This corrects the article DOI: 10.5334/tohm.464.].
5.
Trouillard O, Dupaigne P, Dunoyer M, Doulazmi M, Herlin M, Frismand S, et al.
J Med Genet
. 2023 Jun;
60(11):1116-1126.
PMID: 37308287
Background: Mirror movements are involuntary movements of one hand that mirror intentional movements of the other hand. Congenital mirror movements (CMM) is a rare genetic disorder with autosomal dominant inheritance,...
6.
Moretti R, Arnaud L, Bouteiller D, Trouillard O, Moreau P, Buratti J, et al.
Eur J Paediatr Neurol
. 2021 Jun;
33:121-124.
PMID: 34174751
Background: Variants in SCN1A gene, encoding the voltage-gated sodium channel Na1.1, are associated with distinct epilepsy syndromes ranging from the relatively benign genetic epilepsy with febrile seizures plus (GEFS+) to...
7.
Depienne C, Ciura S, Trouillard O, Bouteiller D, Leitao E, Nava C, et al.
Tremor Other Hyperkinet Mov (N Y)
. 2019 Dec;
9.
PMID: 31824749
Background: Genes involved in Tourette syndrome (TS) remain largely unknown. We aimed to identify genetic factors contributing to TS in a French cohort of 120 individuals using a combination of...
8.
Welniarz Q, Gallea C, Lamy J, Meneret A, Popa T, Valabregue R, et al.
Hum Brain Mapp
. 2019 Jan;
40(7):2125-2142.
PMID: 30653778
The execution of coordinated hand movements requires complex interactions between premotor and primary motor areas in the two hemispheres. The supplementary motor area (SMA) is involved in movement preparation and...
9.
Marsh A, Edwards T, Galea C, Cooper H, Engle E, Jamuar S, et al.
Hum Mutat
. 2017 Oct;
39(1):23-39.
PMID: 29068161
The deleted in colorectal cancer (DCC) gene encodes the netrin-1 (NTN1) receptor DCC, a transmembrane protein required for the guidance of commissural axons. Germline DCC mutations disrupt the development of...
10.
Meneret A, Franz E, Trouillard O, Oliver T, Zagar Y, Robertson S, et al.
J Clin Invest
. 2017 Sep;
127(11):3923-3936.
PMID: 28945198
Netrin-1 is a secreted protein that was first identified 20 years ago as an axon guidance molecule that regulates midline crossing in the CNS. It plays critical roles in various...