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Molecular and clinical analyses with neuropsychological assessment of a case of del(10)(q26.2qter) without intellectual disability: Genomic and transcriptomic combined approach and review of the literature.
Laudier B, Epiais T, Pâris A, Menuet A, Briault S, Ozsancak C, Perche O. Laudier B, et al. Among authors: paris a. Am J Med Genet A. 2016 Jul;170(7):1806-12. doi: 10.1002/ajmg.a.37677. Epub 2016 Apr 26. Am J Med Genet A. 2016. PMID: 27113058 Review.
Early Retinal Defects in Fmr1-/y Mice: Toward a Critical Role of Visual Dys-Sensitivity in the Fragile X Syndrome Phenotype?
Perche O, Felgerolle C, Ardourel M, Bazinet A, Pâris A, Rossignol R, Meyer-Dilhet G, Mausset-Bonnefont AL, Hébert B, Laurenceau D, Montécot-Dubourg C, Menuet A, Bizot JC, Pichon J, Ranchon-Cole I, Briault S. Perche O, et al. Among authors: paris a. Front Cell Neurosci. 2018 Apr 6;12:96. doi: 10.3389/fncel.2018.00096. eCollection 2018. Front Cell Neurosci. 2018. PMID: 29681800 Free PMC article.
FMR protein: Evidence of an emerging role in retinal aging?
Ardourel M, Ranchon-Cole I, Pâris A, Felgerolle C, Acar N, Lesne F, Briault S, Perche O. Ardourel M, et al. Among authors: paris a. Exp Eye Res. 2022 Dec;225:109282. doi: 10.1016/j.exer.2022.109282. Epub 2022 Oct 17. Exp Eye Res. 2022. PMID: 36265576 Free article.
448 results