Passerini I - Search Results

1

Fundus phenotype in retinitis pigmentosa associated with EYS mutations.

Mucciolo DP, Sodi A, Passerini I, Murro V, Cipollini F, Borg I, Pelo E, Contini E, Virgili G, Rizzo S. Mucciolo DP, et al. Among authors: passerini i. Ophthalmic Genet. 2018 Oct;39(5):589-602. doi: 10.1080/13816810.2018.1509351. Epub 2018 Aug 28. Ophthalmic Genet. 2018. PMID: 30153090

2

Melting temperature assay for a UGT1A gene variant in Gilbert syndrome.

Marziliano N, Pelo E, Minuti B, Passerini I, Torricelli F, Da Prato L. Marziliano N, et al. Among authors: passerini i. Clin Chem. 2000 Mar;46(3):423-5. Clin Chem. 2000. PMID: 10702534 No abstract available.

3

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

4

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

5

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

6

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

7

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

8

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

9

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

10

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

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