Torricelli F - Search Results

1

A novel mutation in the VMD2 gene in an Italian family with Best maculopathy.

Sodi A, Passerini I, Simonelli F, Testa F, Menchini U, Torricelli F. Sodi A, et al. Among authors: torricelli f. J Fr Ophtalmol. 2007 Jun;30(6):616-20. doi: 10.1016/s0181-5512(07)89667-7. J Fr Ophtalmol. 2007. PMID: 17646752

2

Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients.

Sodi A, Menchini F, Manitto MP, Passerini I, Murro V, Torricelli F, Menchini U. Sodi A, et al. Among authors: torricelli f. Mol Vis. 2011;17:3078-87. Epub 2011 Nov 24. Mol Vis. 2011. PMID: 22162627 Free PMC article.

3

BEST1 sequence variants in Italian patients with vitelliform macular dystrophy.

Sodi A, Passerini I, Murro V, Caputo R, Bacci GM, Bodoj M, Torricelli F, Menchini U. Sodi A, et al. Among authors: torricelli f. Mol Vis. 2012;18:2736-48. Epub 2012 Nov 17. Mol Vis. 2012. PMID: 23213274 Free PMC article.

4

Occurrence of full-thickness macular hole complicating Stargardt disease with ABCR mutation.

Sodi A, Bini A, Passerini I, Menchini U, Torricelli F. Sodi A, et al. Among authors: torricelli f. Eur J Ophthalmol. 2006 Mar-Apr;16(2):335-8. doi: 10.1177/112067210601600223. Eur J Ophthalmol. 2006. PMID: 16703556

5

A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene.

Testa F, Rossi S, Passerini I, Sodi A, Di Iorio V, Interlandi E, Della Corte M, Menchini U, Rinaldi E, Torricelli F, Simonelli F. Testa F, et al. Among authors: torricelli f. Br J Ophthalmol. 2008 Nov;92(11):1467-70. doi: 10.1136/bjo.2008.143776. Epub 2008 Aug 14. Br J Ophthalmol. 2008. PMID: 18703557

6

Different patterns of fundus autofluorescence related to ABCA4 gene mutations in Stargardt disease.

Sodi A, Bini A, Passerini I, Forconi S, Menchini U, Torricelli F. Sodi A, et al. Among authors: torricelli f. Ophthalmic Surg Lasers Imaging. 2010 Jan-Feb;41(1):48-53. doi: 10.3928/15428877-20091230-09. Ophthalmic Surg Lasers Imaging. 2010. PMID: 20128570

7

Variable expressivity of abca4 gene mutations in an italian family with stargardt disease.

Sodi A, Bini A, Passerini I, Puccioni M, Torricelli F, Menchini U. Sodi A, et al. Among authors: torricelli f. Retin Cases Brief Rep. 2008 Winter;2(1):80-2. doi: 10.1097/01.iae.0000249397.40151.96. Retin Cases Brief Rep. 2008. PMID: 25389627

8

MYO7A and USH2A gene sequence variants in Italian patients with Usher syndrome.

Sodi A, Mariottini A, Passerini I, Murro V, Tachyla I, Bianchi B, Menchini U, Torricelli F. Sodi A, et al. Among authors: torricelli f. Mol Vis. 2014 Dec 23;20:1717-31. eCollection 2014. Mol Vis. 2014. PMID: 25558175 Free PMC article.

9

Phenotypic intrafamilial variability associated with S212G mutation in the RDS/peripherin gene.

Passerini I, Sodi A, Giambene B, Menchini U, Torricelli F. Passerini I, et al. Among authors: torricelli f. Eur J Ophthalmol. 2007 Nov-Dec;17(6):1000-3. doi: 10.1177/112067210701700624. Eur J Ophthalmol. 2007. PMID: 18050133

10

Novel mutations in of the ABCR gene in Italian patients with Stargardt disease.

Passerini I, Sodi A, Giambene B, Mariottini A, Menchini U, Torricelli F. Passerini I, et al. Among authors: torricelli f. Eye (Lond). 2010 Jan;24(1):158-64. doi: 10.1038/eye.2009.35. Epub 2009 Mar 6. Eye (Lond). 2010. PMID: 19265867

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