Olivier Perche
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Explore the profile of Olivier Perche including associated specialties, affiliations and a list of published articles.
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Articles
31
Citations
431
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Recent Articles
1.
Attallah A, Ardourel M, Gallazzini F, Lesne F, De Oliveira A, Togbe D, et al.
Exp Eye Res
. 2024 Aug;
246:110015.
PMID: 39089568
Fragile X Syndrome (FXS), the most common inherited form of human intellectual disability, is a monogenic neurodevelopmental disorder caused by a loss-of-function mutation of the FMR1 gene. FMR1 is encoding...
2.
Attallah A, Ardourel M, Lesne F, De Oliveira A, Felgerolle C, Briault S, et al.
Exp Eye Res
. 2024 Jun;
245:109964.
PMID: 38851478
To prevent ocular pathologies, new generation of dietary supplements have been commercially available. They consist of nutritional supplement mixing components known to provide antioxidative properties, such as unsaturated fatty acid,...
3.
Ardourel M, Paris A, Felgerolle C, Lesne F, Ranchon-Cole I, Briault S, et al.
Exp Eye Res
. 2022 Sep;
224:109238.
PMID: 36067823
FMRP, the fragile X mental retardation protein coded by the FMR1 gene, is an RNA-binding protein that assists transport, stabilization and translational regulation of specific synaptic mRNAs. Its expression has...
4.
Baala L, Benzekri-Lefevre D, Bret L, Guillaume C, Courtellemont L, El Khalil A, et al.
F1000Res
. 2022 May;
9:1482.
PMID: 35528205
Coronavirus disease 2019 (COVID-19) is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and has been a global public health concern. We report coinfection of SARS-CoV-2 and 2009...
5.
Perche O, Lesne F, Patat A, Raab S, Twyman R, Ring R, et al.
J Med Case Rep
. 2022 May;
16(1):180.
PMID: 35509069
Background: Mutations in the genes encoding the large-conductance calcium-activated potassium channel, especially KCNMA1 encoding its α-subunit, have been linked to several neurological features, including intellectual disability or autism. Associated with...
6.
Perche O, Lesne F, Patat A, Raab S, Twyman R, Ring R, et al.
J Neurodev Disord
. 2021 Oct;
13(1):45.
PMID: 34625026
Background: Disturbances in sensory function are an important clinical feature of neurodevelopmental disorders such as fragile X syndrome (FXS). Evidence also directly connects sensory abnormalities with the clinical expression of...
7.
Ardourel M, Felgerolle C, Paris A, Acar N, Ramchani Ben Othman K, Ueda N, et al.
Nutrients
. 2021 Sep;
13(9).
PMID: 34579093
To prevent ocular pathologies, new generation of dietary supplements have been commercially available. They consist of nutritional supplement mixing components known to provide antioxidative properties, such as unsaturated fatty acid,...
8.
Rontani P, Perche O, Greetham L, Jullien N, Gepner B, Feron F, et al.
Mol Psychiatry
. 2020 Apr;
26(5):1606-1618.
PMID: 32327736
Autism spectrum disorders (ASD) are complex neurodevelopmental disorders with a very large number of risk loci detected in the genome. However, at best, each of them explains rare cases, the...
9.
Felgerolle C, Hebert B, Ardourel M, Meyer-Dilhet G, Menuet A, Pinto-Morais K, et al.
Front Behav Neurosci
. 2019 Nov;
13:228.
PMID: 31680892
Fragile X Syndrome (FXS), the most common inherited form of human intellectual disability (ID) associated with autistic-like behaviors, is characterized by dys-sensitivity to sensory stimuli, especially vision. In the absence...
10.
Laviolle B, Perche O, Gueyffier F
Therapie
. 2019 Jan;
74(1):1-8.
PMID: 30616902
No abstract available.