Passerini I - Search Results

1

Optical coherence tomography (OCT) features of cystoid spaces in choroideremia (CHM).

Murro V, Mucciolo DP, Giorgio D, Sodi A, Passerini I, Bacci G, Bargiacchi S, Virgili G, Rizzo S. Murro V, et al. Among authors: passerini i. Graefes Arch Clin Exp Ophthalmol. 2019 Dec;257(12):2655-2663. doi: 10.1007/s00417-019-04508-7. Epub 2019 Oct 26. Graefes Arch Clin Exp Ophthalmol. 2019. PMID: 31654189

2

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: passerini i. Eur J Ophthalmol. 2006 Mar-Apr;16(2):335-8. doi: 10.1177/112067210601600223. Eur J Ophthalmol. 2006. PMID: 16703556

3

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: passerini i. J Fr Ophtalmol. 2007 Jun;30(6):616-20. doi: 10.1016/s0181-5512(07)89667-7. J Fr Ophtalmol. 2007. PMID: 17646752

4

Retinal astrocytic hamartoma and Stargardt's disease: unusual association in a patient with ABCR mutation without phacomatosis.

Bini A, Sodi A, Passerini I, Menchini U, Torricelli F. Bini A, et al. Among authors: passerini i. Clin Exp Ophthalmol. 2007 Nov;35(8):777-9. doi: 10.1111/j.1442-9071.2007.01582.x. Clin Exp Ophthalmol. 2007. PMID: 17997789

5

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. Eur J Ophthalmol. 2007 Nov-Dec;17(6):1000-3. doi: 10.1177/112067210701700624. Eur J Ophthalmol. 2007. PMID: 18050133

6

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: passerini i. 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

7

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. Eye (Lond). 2010 Jan;24(1):158-64. doi: 10.1038/eye.2009.35. Epub 2009 Mar 6. Eye (Lond). 2010. PMID: 19265867

8

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: passerini i. Ophthalmic Surg Lasers Imaging. 2010 Jan-Feb;41(1):48-53. doi: 10.3928/15428877-20091230-09. Ophthalmic Surg Lasers Imaging. 2010. PMID: 20128570

9

Novel RDH12 sequence variations in Leber congenital amaurosis.

Sodi A, Caputo R, Passerini I, Bacci GM, Menchini U. Sodi A, et al. Among authors: passerini i. J AAPOS. 2010 Aug;14(4):349-51. doi: 10.1016/j.jaapos.2010.04.010. J AAPOS. 2010. PMID: 20736127

10

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: passerini i. Mol Vis. 2011;17:3078-87. Epub 2011 Nov 24. Mol Vis. 2011. PMID: 22162627 Free PMC article.

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