Passerini I - Search Results

1

A novel mutation of BEST1 gene in Best disease.

Campa C, Parmeggiani F, Spena R, Ognibene D, Passerini I, Gualandi F. Campa C, et al. Among authors: passerini i. Eur J Ophthalmol. 2021 May;31(3):NP93-NP95. doi: 10.1177/1120672120920536. Epub 2020 Apr 22. Eur J Ophthalmol. 2021. PMID: 32321300

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

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

4

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

5

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.

6

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: passerini i. Mol Vis. 2012;18:2736-48. Epub 2012 Nov 17. Mol Vis. 2012. PMID: 23213274 Free PMC article.

7

Homozygous c.1937+1G>A splice-site variant of the ABCA4 gene is associated with Stargardt disease.

Eandi CM, Grignolo FM, Passerini I, Marchese C. Eandi CM, et al. Among authors: passerini i. Eur J Ophthalmol. 2014 Sep-Oct;24(5):814-7. doi: 10.5301/ejo.5000458. Epub 2014 Feb 24. Eur J Ophthalmol. 2014. PMID: 24585425

8

Long-Term Results of Photodynamic Therapy for Choroidal Neovascularization in Pediatric Patients with Best Vitelliform Macular Dystrophy.

Sodi A, Murro V, Caporossi O, Passerini I, Bacci GM, Caputo R, Menchini U. Sodi A, et al. Among authors: passerini i. Ophthalmic Genet. 2015 Jun;36(2):168-74. doi: 10.3109/13816810.2015.1009121. Epub 2015 Feb 12. Ophthalmic Genet. 2015. PMID: 25675349

9

EDI-OCT evaluation of choroidal thickness in retinitis pigmentosa.

Sodi A, Lenzetti C, Murro V, Caporossi O, Mucciolo DP, Bacherini D, Cipollini F, Passerini I, Virgili G, Rizzo S. Sodi A, et al. Among authors: passerini i. Eur J Ophthalmol. 2018 Jan;28(1):52-57. doi: 10.5301/ejo.5000961. Eur J Ophthalmol. 2018. PMID: 28604982

10

The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement.

Black GC, Sergouniotis P, Sodi A, Leroy BP, Van Cauwenbergh C, Liskova P, Grønskov K, Klett A, Kohl S, Taurina G, Sukys M, Haer-Wigman L, Nowomiejska K, Marques JP, Leroux D, Cremers FPM, De Baere E, Dollfus H; ERN-EYE study group. Black GC, et al. Orphanet J Rare Dis. 2021 Mar 20;16(1):142. doi: 10.1186/s13023-021-01756-x. Orphanet J Rare Dis. 2021. PMID: 33743793 Free PMC article.

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