Meunier I - Search Results

1

Extensive macular atrophy with pseudodrusen-like appearance: a new clinical entity.

Hamel CP, Meunier I, Arndt C, Ben Salah S, Lopez S, Bazalgette C, Bazalgette C, Zanlonghi X, Arnaud B, Defoort-Dellhemmes S, Puech B. Hamel CP, et al. Among authors: meunier i. Am J Ophthalmol. 2009 Apr;147(4):609-20. doi: 10.1016/j.ajo.2008.10.022. Epub 2009 Feb 1. Am J Ophthalmol. 2009. PMID: 19181301

2

ROSAH syndrome mimicking chronic uveitis.

Fardeau C, Alafaleq M, Dhaenens CM, Dollfus H, Koné-Paut I, Grunewald O, Morel JB, Titah C, Saadoun D, Lazeran PO, Meunier I. Fardeau C, et al. Among authors: meunier i. Clin Genet. 2023 Apr;103(4):453-458. doi: 10.1111/cge.14286. Epub 2022 Dec 30. Clin Genet. 2023. PMID: 36543582

3

[Congenital dystrophy: unilateral involvement in vitelliform retinal dystrophy or Best disease].

Meunier I, Ben Salah S, Arndt C, Hamel C. Meunier I, et al. J Fr Ophtalmol. 2008 Jun;31(6 Pt 1):640-1. doi: 10.1016/s0181-5512(08)75471-8. J Fr Ophtalmol. 2008. PMID: 18772821 French. No abstract available.

4

[Retinitis pigmentosa and central serous choroiditis. Retinal imaging and optical coherence tomography views].

Meunier I, Ben Salah S, Arndt C, Hamel C. Meunier I, et al. J Fr Ophtalmol. 2008 Sep;31(7):735. doi: 10.1016/s0181-5512(08)74392-4. J Fr Ophtalmol. 2008. PMID: 18971860 French. No abstract available.

5

Unilateral retinal pigment epithelium dysgenesis.

Cohen SY, Fung AE, Tadayoni R, Massin P, Barbazetto I, Berthout A, Gayet P, Meunier I, Yannuzzi LA. Cohen SY, et al. Among authors: meunier i. Am J Ophthalmol. 2009 Dec;148(6):914-9.e2. doi: 10.1016/j.ajo.2009.06.033. Epub 2009 Sep 5. Am J Ophthalmol. 2009. PMID: 19733831

6

Electrophysiological retinal pigment epithelium changes observed with indocyanine green, trypan blue and triamcinolone.

Arndt C, Meunier I, Rebollo O, Martinenq C, Hamel C, Hattenbach LO. Arndt C, et al. Among authors: meunier i. Ophthalmic Res. 2010;44(1):17-23. doi: 10.1159/000279437. Epub 2010 Feb 3. Ophthalmic Res. 2010. PMID: 20130442

7

Screening genes of the visual cycle RGR, RBP1 and RBP3 identifies rare sequence variations.

Ksantini M, Sénéchal A, Bocquet B, Meunier I, Brabet P, Hamel CP. Ksantini M, et al. Among authors: meunier i. Ophthalmic Genet. 2010 Dec;31(4):200-4. doi: 10.3109/13816810.2010.512354. Ophthalmic Genet. 2010. PMID: 21067480

8

Systematic screening of BEST1 and PRPH2 in juvenile and adult vitelliform macular dystrophies: a rationale for molecular analysis.

Meunier I, Sénéchal A, Dhaenens CM, Arndt C, Puech B, Defoort-Dhellemmes S, Manes G, Chazalette D, Mazoir E, Bocquet B, Hamel CP. Meunier I, et al. Ophthalmology. 2011 Jun;118(6):1130-6. doi: 10.1016/j.ophtha.2010.10.010. Epub 2011 Jan 26. Ophthalmology. 2011. PMID: 21269699

9

A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1.

Manes G, Hebrard M, Bocquet B, Meunier I, Coustes-Chazalette D, Sénéchal A, Bolland-Augé A, Zelenika D, Hamel CP. Manes G, et al. Among authors: meunier i. BMC Med Genet. 2011 Apr 15;12:54. doi: 10.1186/1471-2350-12-54. BMC Med Genet. 2011. PMID: 21496248 Free PMC article.

10

[Screening for retinal detachment using wide-field retinal imaging].

Bonnay G, Nguyen F, Meunier I, Ducasse A, Hamel C, Arndt C. Bonnay G, et al. Among authors: meunier i. J Fr Ophtalmol. 2011 Sep;34(7):482-5. doi: 10.1016/j.jfo.2011.02.012. Epub 2011 May 31. J Fr Ophtalmol. 2011. PMID: 21621874 French.

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