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Retinitis pigmentosa and other dystrophies.
Sahel J, Bonnel S, Mrejen S, Paques M. Sahel J, et al. Among authors: paques m. Dev Ophthalmol. 2010;47:160-167. doi: 10.1159/000320079. Epub 2010 Aug 10. Dev Ophthalmol. 2010. PMID: 20703049 Review.
Foveal shape and structure in a normal population.
Tick S, Rossant F, Ghorbel I, Gaudric A, Sahel JA, Chaumet-Riffaud P, Paques M. Tick S, et al. Among authors: paques m. Invest Ophthalmol Vis Sci. 2011 Jul 29;52(8):5105-10. doi: 10.1167/iovs.10-7005. Invest Ophthalmol Vis Sci. 2011. PMID: 21803966 Clinical Trial.
Adaptive optics imaging of geographic atrophy.
Gocho K, Sarda V, Falah S, Sahel JA, Sennlaub F, Benchaboune M, Ullern M, Paques M. Gocho K, et al. Among authors: paques m. Invest Ophthalmol Vis Sci. 2013 May 1;54(5):3673-80. doi: 10.1167/iovs.12-10672. Invest Ophthalmol Vis Sci. 2013. PMID: 23620431 Clinical Trial.
Recognition of Henle's fiber layer on OCT images.
Mrejen S, Gallego-Pinazo R, Freund KB, Paques M. Mrejen S, et al. Among authors: paques m. Ophthalmology. 2013 Jun;120(6):e32-3.e1. doi: 10.1016/j.ophtha.2013.01.039. Ophthalmology. 2013. PMID: 23732066 No abstract available.
The familial dementia gene revisited: a missense mutation revealed by whole-exome sequencing identifies ITM2B as a candidate gene underlying a novel autosomal dominant retinal dystrophy in a large family.
Audo I, Bujakowska K, Orhan E, El Shamieh S, Sennlaub F, Guillonneau X, Antonio A, Michiels C, Lancelot ME, Letexier M, Saraiva JP, Nguyen H, Luu TD, Léveillard T, Poch O, Dollfus H, Paques M, Goureau O, Mohand-Saïd S, Bhattacharya SS, Sahel JA, Zeitz C. Audo I, et al. Among authors: paques m. Hum Mol Genet. 2014 Jan 15;23(2):491-501. doi: 10.1093/hmg/ddt439. Epub 2013 Sep 10. Hum Mol Genet. 2014. PMID: 24026677
240 results