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Poppers-associated retinal toxicity.
Vignal-Clermont C, Audo I, Sahel JA, Paques M. Vignal-Clermont C, et al. Among authors: audo i. N Engl J Med. 2010 Oct 14;363(16):1583-5. doi: 10.1056/NEJMc1005118. N Engl J Med. 2010. PMID: 20942681 No abstract available.
Evaluation of retinal function and flicker light-induced retinal vascular response in normotensive patients with diabetes without retinopathy.
Lecleire-Collet A, Audo I, Aout M, Girmens JF, Sofroni R, Erginay A, Le Gargasson JF, Mohand-Saïd S, Meas T, Guillausseau PJ, Vicaut E, Paques M, Massin P. Lecleire-Collet A, et al. Among authors: audo i. Invest Ophthalmol Vis Sci. 2011 May 2;52(6):2861-7. doi: 10.1167/iovs.10-5960. Invest Ophthalmol Vis Sci. 2011. PMID: 21282578 Clinical Trial.
Foveal damage in habitual poppers users.
Audo I, El Sanharawi M, Vignal-Clermont C, Villa A, Morin A, Conrath J, Fompeydie D, Sahel JA, Gocho-Nakashima K, Goureau O, Paques M. Audo I, et al. Arch Ophthalmol. 2011 Jun;129(6):703-8. doi: 10.1001/archophthalmol.2011.6. Epub 2011 Feb 14. Arch Ophthalmol. 2011. PMID: 21320953
Retinal degeneration in mucopolysaccharidose type II.
Liang F, Audo I, Sahel JA, Paques M. Liang F, et al. Among authors: audo i. Graefes Arch Clin Exp Ophthalmol. 2013 Jul;251(7):1871-2. doi: 10.1007/s00417-012-2215-1. Epub 2012 Dec 4. Graefes Arch Clin Exp Ophthalmol. 2013. PMID: 23208705 No abstract available.
Relative frequencies of inherited retinal dystrophies and optic neuropathies in Southern France: assessment of 21-year data management.
Bocquet B, Lacroux A, Surget MO, Baudoin C, Marquette V, Manes G, Hebrard M, Sénéchal A, Delettre C, Roux AF, Claustres M, Dhaenens CM, Rozet JM, Perrault I, Bonnefont JP, Kaplan J, Dollfus H, Amati-Bonneau P, Bonneau D, Reynier P, Audo I, Zeitz C, Sahel JA, Paquis-Flucklinger V, Calvas P, Arveiler B, Kohl S, Wissinger B, Blanchet C, Meunier I, Hamel CP. Bocquet B, et al. Among authors: audo i. Ophthalmic Epidemiol. 2013;20(1):13-25. doi: 10.3109/09286586.2012.737890. Ophthalmic Epidemiol. 2013. PMID: 23350551
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. 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
High prevalence of PRPH2 in autosomal dominant retinitis pigmentosa in france and characterization of biochemical and clinical features.
Manes G, Guillaumie T, Vos WL, Devos A, Audo I, Zeitz C, Marquette V, Zanlonghi X, Defoort-Dhellemmes S, Puech B, Said SM, Sahel JA, Odent S, Dollfus H, Kaplan J, Dufier JL, Le Meur G, Weber M, Faivre L, Cohen FB, Béroud C, Picot MC, Verdier C, Sénéchal A, Baudoin C, Bocquet B, Findlay JB, Meunier I, Dhaenens CM, Hamel CP. Manes G, et al. Among authors: audo i. Am J Ophthalmol. 2015 Feb;159(2):302-14. doi: 10.1016/j.ajo.2014.10.033. Epub 2014 Nov 5. Am J Ophthalmol. 2015. PMID: 25447119 Free article.
215 results