Fabien Lesne
14 Avenue De L'Hôpital
Orleans, 45100, France
Orleans, 45100, France
Last Updated: 09/26/2026
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Found 14 publications
Lack of FMRP in the retina: Evidence of a retinal specific transcriptomic profile.
Journal: Experimental eye research
Published: March 27, 2024
Dietary supplement enriched in antioxidants and omega-3 promotes retinal glutamine synthesis.
Journal: Experimental eye research
Published: February 16, 2024
Comparing the intraocular pressure values obtained with a rebound tonometer (TONOVET Plus) and an indentation tonometer (IOPvet) in dogs with and without ocular disease.
Journal: The Veterinary record
Published: January 17, 2024
Diagnostic accuracy of a rapid antigen triple test (SARS-CoV-2, respiratory syncytial virus, and influenza) using anterior nasal swabs versus multiplex RT-PCR in children in an emergency department.
Journal: Infectious diseases now
Published: June 30, 2023
FMR protein: Evidence of an emerging role in retinal aging?
Journal: Experimental eye research
Published: August 11, 2022
FMRP-related retinal phenotypes: Evidence of glutamate-glutamine metabolic cycle impairment.
Journal: Experimental eye research
Published: June 28, 2022
Large-conductance calcium-activated potassium channel haploinsufficiency leads to sensory deficits in the visual system: a case report.
Journal: Journal of medical case reports
Published: January 10, 2022
Effect of Tenofovir Disoproxil Fumarate and Emtricitabine on nasopharyngeal SARS-CoV-2 viral load burden amongst outpatients with COVID-19: A pilot, randomized, open-label phase 2 trial.
Journal: EClinicalMedicine
Published: May 18, 2021
Electroretinography and contrast sensitivity, complementary translational biomarkers of sensory deficits in the visual system of individuals with fragile X syndrome.
Journal: Journal of neurodevelopmental disorders
Published: April 08, 2021
Copy Number Variations Found in Patients with a Corpus Callosum Abnormality and Intellectual Disability.
Journal: The Journal of pediatrics
Published: September 29, 2016
ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability.
Journal: Brain : a journal of neurology
Published: July 31, 2016
Last Updated: 09/26/2026