Meunier I - Search Results

1

Pathogenicity of novel atypical variants leading to choroideremia as determined by functional analyses.

Vaché C, Torriano S, Faugère V, Erkilic N, Baux D, Garcia-Garcia G, Hamel CP, Meunier I, Zanlonghi X, Koenig M, Kalatzis V, Roux AF. Vaché C, et al. Among authors: meunier i. Hum Mutat. 2019 Jan;40(1):31-35. doi: 10.1002/humu.23671. Epub 2018 Nov 8. Hum Mutat. 2019. PMID: 30341801

2

[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.

3

[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.

4

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

5

Mutations in CNNM4 cause recessive cone-rod dystrophy with amelogenesis imperfecta.

Polok B, Escher P, Ambresin A, Chouery E, Bolay S, Meunier I, Nan F, Hamel C, Munier FL, Thilo B, Mégarbané A, Schorderet DF. Polok B, et al. Among authors: meunier i. Am J Hum Genet. 2009 Feb;84(2):259-65. doi: 10.1016/j.ajhg.2009.01.006. Epub 2009 Feb 5. Am J Hum Genet. 2009. PMID: 19200527 Free PMC article.

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

Cataract as a phenotypic marker for a mutation in WFS1, the Wolfram syndrome gene.

Titah SM, Meunier I, Blanchet C, Lopez S, Rondouin G, Lenaers G, Amati-Bonneau P, Reynier P, Paquis-Flucklinger V, Hamel CP. Titah SM, et al. Among authors: meunier i. Eur J Ophthalmol. 2012 Mar-Apr;22(2):254-8. doi: 10.5301/EJO.2011.8370. Eur J Ophthalmol. 2012. PMID: 21623591 Free article.

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