Munier FL - Search Results

1

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

2

Subretinal neovascularization secondary to choroidal septic metastasis from acute bacterial endocarditis.

Munier F, Othenin-Girard P. Munier F, et al. Retina. 1992;12(2):108-12. doi: 10.1097/00006982-199212020-00006. Retina. 1992. PMID: 1439240

3

[Familial uveal melanoma].

Bercher L, Munier F, Zografos L, Schorderet D, Egger E, Chamot L. Bercher L, et al. Klin Monbl Augenheilkd. 1995 May;206(5):384-7. doi: 10.1055/s-2008-1035470. Klin Monbl Augenheilkd. 1995. PMID: 7609394 French.

4

Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21.

Héon E, Piguet B, Munier F, Sneed SR, Morgan CM, Forni S, Pescia G, Schorderet D, Taylor CM, Streb LM, Wiles CD, Nishimura DY, Sheffield VC, Stone EM. Héon E, et al. Arch Ophthalmol. 1996 Feb;114(2):193-8. doi: 10.1001/archopht.1996.01100130187014. Arch Ophthalmol. 1996. PMID: 8573024

5

Sex mutation ratio in retinoblastoma and retinoma: relevance to genetic counseling.

Munier FL, Thonney F, Balmer A, Héon E, Pescia G, Schorderet DF. Munier FL, et al. Klin Monbl Augenheilkd. 1996 May;208(5):400-3. doi: 10.1055/s-2008-1035252. Klin Monbl Augenheilkd. 1996. PMID: 8766064

6

[Oncogenes and anti-oncogenes: the genetics of cancer].

Schorderet DF, Munier FL. Schorderet DF, et al. Among authors: munier fl. Praxis (Bern 1994). 1996 Aug 27;85(35):1019-22. Praxis (Bern 1994). 1996. PMID: 8848670 French.

7

[Retinoblastoma: clinical and molecular diagnostic aspects].

Thonney F, Munier FL, Balmer A, Pescia G, Schorderet DF. Thonney F, et al. Among authors: munier fl. Praxis (Bern 1994). 1996 Aug 27;85(35):1058-62. Praxis (Bern 1994). 1996. PMID: 8848678 Review. French.

8

Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies Groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOX.

Korvatska E, Munier FL, Zografos L, Ahmad F, Faggioni R, Dolivo-Beuret A, Uffer S, Pescia G, Schorderet DF. Korvatska E, et al. Among authors: munier fl. Eur J Hum Genet. 1996;4(4):214-8. doi: 10.1159/000472201. Eur J Hum Genet. 1996. PMID: 8875187

9

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

10

Kerato-epithelin mutations in four 5q31-linked corneal dystrophies.

Munier FL, Korvatska E, Djemaï A, Le Paslier D, Zografos L, Pescia G, Schorderet DF. Munier FL, et al. Nat Genet. 1997 Mar;15(3):247-51. doi: 10.1038/ng0397-247. Nat Genet. 1997. PMID: 9054935

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