Munier F - Search Results

1

Optical coherence tomography morphology and evolution in cblC disease-related maculopathy in a case series of very young patients.

Bacci GM, Donati MA, Pasquini E, Munier F, Cavicchi C, Morrone A, Sodi A, Murro V, Garcia Segarra N, Defilippi C, Bussolin L, Caputo R. Bacci GM, et al. Among authors: munier f. Acta Ophthalmol. 2017 Dec;95(8):e776-e782. doi: 10.1111/aos.13441. Epub 2017 May 8. Acta Ophthalmol. 2017. PMID: 28481040 Free article.

2

[Optical coherence tomography in Malattia Leventinese].

Gaillard MC, Wolfensberger TJ, Uffer S, Mantel I, Pournaras JA, Schorderet DF, Munier FL. Gaillard MC, et al. Among authors: munier fl. Klin Monbl Augenheilkd. 2005 Mar;222(3):180-5. doi: 10.1055/s-2005-857972. Klin Monbl Augenheilkd. 2005. PMID: 15785976 French.

3

Optical coherence tomography (OCT) to image active and inactive retinoblastomas as well as retinomas.

Nadiarnykh O, McNeill-Badalova NA, Gaillard MC, Bosscha MI, Fabius AWM, Verbraak FD, Munier FL, de Boer JF, Moll AC. Nadiarnykh O, et al. Among authors: munier fl. Acta Ophthalmol. 2020 Mar;98(2):158-165. doi: 10.1111/aos.14214. Epub 2019 Aug 26. Acta Ophthalmol. 2020. PMID: 31448879 Free PMC article.

4

Full characterization of the maculopathy associated with an Arg-172-Trp mutation in the RDS/peripherin gene.

Piguet B, Héon E, Munier FL, Grounauer PA, Niemeyer G, Butler N, Schorderet DF, Sheffield VC, Stone EM. Piguet B, et al. Among authors: munier fl. Ophthalmic Genet. 1996 Dec;17(4):175-86. doi: 10.3109/13816819609057891. Ophthalmic Genet. 1996. PMID: 9010868

5

Evanescent white linear flecks and posterior microphthalmos: new features of a recently established disease.

Tran HV, Borruat FX, Reymond-Gruber S, Schorderet D, Munier F. Tran HV, et al. Among authors: munier f. Klin Monbl Augenheilkd. 2006 May;223(5):397-9. doi: 10.1055/s-2006-926563. Klin Monbl Augenheilkd. 2006. PMID: 16705514

6

Retinal dystrophy in the oculo-auricular syndrome due to HMX1 mutation.

Vaclavik V, Schorderet DF, Borruat FX, Munier FL. Vaclavik V, et al. Among authors: munier fl. Ophthalmic Genet. 2011 Jun;32(2):114-7. doi: 10.3109/13816810.2011.562955. Epub 2011 Mar 18. Ophthalmic Genet. 2011. PMID: 21417677

7

Pattern dystrophy with high intrafamilial variability associated with Y141C mutation in the peripherin/RDS gene and successful treatment of subfoveal CNV related to multifocal pattern type with anti-VEGF (ranibizumab) intravitreal injections.

Vaclavik V, Tran HV, Gaillard MC, Schorderet DF, Munier FL. Vaclavik V, et al. Among authors: munier fl. Retina. 2012 Oct;32(9):1942-9. doi: 10.1097/IAE.0b013e31824b32e4. Retina. 2012. PMID: 22466463

8

SUBFOVEAL NODULE IN COATS' DISEASE: Toward an Updated Classification Predicting Visual Prognosis.

Daruich AL, Moulin AP, Tran HV, Matet A, Munier FL. Daruich AL, et al. Retina. 2017 Aug;37(8):1591-1598. doi: 10.1097/IAE.0000000000001399. Retina. 2017. PMID: 28030429 Free PMC article.

9

Variability in clinical phenotypes of PRPF8-linked autosomal dominant retinitis pigmentosa correlates with differential PRPF8/SNRNP200 interactions.

Escher P, Passarin O, Munier FL, Tran VH, Vaclavik V. Escher P, et al. Ophthalmic Genet. 2018 Jan-Feb;39(1):80-86. doi: 10.1080/13816810.2017.1393825. Epub 2017 Oct 31. Ophthalmic Genet. 2018. PMID: 29087248

10

Successful conservative treatment of massive choroidal relapse in 2 retinoblastoma patients monitored by ultrasound biomicroscopy and/or spectral domain optic coherence tomography.

Stathopoulos C, Gaillard MC, Puccinelli F, Maeder P, Hadjistilianou D, Beck-Popovic M, Munier FL. Stathopoulos C, et al. Among authors: munier fl. Ophthalmic Genet. 2018 Apr;39(2):242-246. doi: 10.1080/13816810.2017.1393826. Epub 2017 Nov 3. Ophthalmic Genet. 2018. PMID: 29099668

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