Sahel JA - Search Results

1

ARL2BP mutations account for 0.1% of autosomal recessive rod-cone dystrophies with the report of a novel splice variant.

Audo I, El Shamieh S, Méjécase C, Michiels C, Demontant V, Antonio A, Condroyer C, Boyard F, Letexier M, Saraiva JP, Blanchard S, Mohand-Saïd S, Sahel JA, Zeitz C. Audo I, et al. Among authors: sahel ja. Clin Genet. 2017 Jul;92(1):109-111. doi: 10.1111/cge.12909. Epub 2017 Feb 6. Clin Genet. 2017. PMID: 27790702

2

[Hereditary retinal pathologies and AMD: new therapeutic perspectives].

Bonnel S, Mohand-Said S, Barale PO, De Nicola R, Sahel JA. Bonnel S, et al. Among authors: sahel ja. J Fr Ophtalmol. 2004 Jun;27(6 Pt 1):623-33. doi: 10.1016/s0181-5512(04)96188-8. J Fr Ophtalmol. 2004. PMID: 15343122 Review. French.

3

Next-generation sequencing confirms the implication of SLC24A1 in autosomal-recessive congenital stationary night blindness.

Neuillé M, Malaichamy S, Vadalà M, Michiels C, Condroyer C, Sachidanandam R, Srilekha S, Arokiasamy T, Letexier M, Démontant V, Sahel JA, Sen P, Audo I, Soumittra N, Zeitz C. Neuillé M, et al. Among authors: sahel ja. Clin Genet. 2016 Jun;89(6):690-9. doi: 10.1111/cge.12746. Epub 2016 Mar 4. Clin Genet. 2016. PMID: 26822852

4

Multimodal imaging and functional correlations identify unusual cases of macular retinal pigment epithelium hypopigmentation occurring without functional loss.

Boulanger-Scemama E, Akesbi J, Tick S, Mohand-Said S, Sahel JA, Audo I. Boulanger-Scemama E, et al. Among authors: sahel ja. Doc Ophthalmol. 2017 Aug;135(1):77-83. doi: 10.1007/s10633-017-9592-z. Epub 2017 Jun 7. Doc Ophthalmol. 2017. PMID: 28593392

5

A novel nonsense variant in REEP6 is involved in a sporadic rod-cone dystrophy case.

Méjécase C, Mohand-Saïd S, El Shamieh S, Antonio A, Condroyer C, Blanchard S, Letexier M, Saraiva JP, Sahel JA, Audo I, Zeitz C. Méjécase C, et al. Among authors: sahel ja. Clin Genet. 2018 Mar;93(3):707-711. doi: 10.1111/cge.13171. Clin Genet. 2018. PMID: 29120066

6

Of fluid and tubes.

Nassisi M, Sahel JA, Audo I. Nassisi M, et al. Among authors: sahel ja. J Fr Ophtalmol. 2021 Feb;44(2):277-278. doi: 10.1016/j.jfo.2020.04.028. Epub 2020 Nov 1. J Fr Ophtalmol. 2021. PMID: 33139087 No abstract available.

7

[CRISPR/Cas9: From research to therapeutic application].

Ben Yacoub T, Wohlschlegel J, Sahel JA, Zeitz C, Audo I. Ben Yacoub T, et al. Among authors: sahel ja. J Fr Ophtalmol. 2023 Apr;46(4):398-407. doi: 10.1016/j.jfo.2022.10.008. Epub 2023 Feb 8. J Fr Ophtalmol. 2023. PMID: 36759244 Free article. Review. French.

8

Thioredoxin rod-derived cone viability factor protects against photooxidative retinal damage.

Elachouri G, Lee-Rivera I, Clérin E, Argentini M, Fridlich R, Blond F, Ferracane V, Yang Y, Raffelsberger W, Wan J, Bennett J, Sahel JA, Zack DJ, Léveillard T. Elachouri G, et al. Among authors: sahel ja. Free Radic Biol Med. 2015 Apr;81:22-9. doi: 10.1016/j.freeradbiomed.2015.01.003. Epub 2015 Jan 14. Free Radic Biol Med. 2015. PMID: 25596499 Free article.

9

Familial central retinal vein occlusion.

Girmens JF, Scheer S, Héron E, Sahel JA, Tournier-Lasserve E, Paques M. Girmens JF, et al. Among authors: sahel ja. Eye (Lond). 2008 Feb;22(2):308-10. doi: 10.1038/sj.eye.6702672. Epub 2006 Dec 15. Eye (Lond). 2008. PMID: 17173011

10

The disruption of the rod-derived cone viability gene leads to photoreceptor dysfunction and susceptibility to oxidative stress.

Cronin T, Raffelsberger W, Lee-Rivera I, Jaillard C, Niepon ML, Kinzel B, Clérin E, Petrosian A, Picaud S, Poch O, Sahel JA, Léveillard T. Cronin T, et al. Among authors: sahel ja. Cell Death Differ. 2010 Jul;17(7):1199-210. doi: 10.1038/cdd.2010.2. Epub 2010 Feb 5. Cell Death Differ. 2010. PMID: 20139892 Free PMC article.

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