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Items: 37

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.

Graefes Arch Clin Exp Ophthalmol. 2019 Dec;257(12):2655-2663. doi: 10.1007/s00417-019-04508-7. Epub 2019 Oct 26.

PMID:
31654189
2.

Near-infrared autofluorescence in young choroideremia patients.

Mucciolo DP, Murro V, Giorgio D, Sodi A, Passerini I, Virgili G, Rizzo S.

Ophthalmic Genet. 2019 Oct;40(5):421-427. doi: 10.1080/13816810.2019.1666881. Epub 2019 Sep 21.

PMID:
31544579
3.

Peculiar Clinical Findings in Young Choroideremia Patients: A Retrospective Case Review.

Mucciolo DP, Murro V, Sodi A, Passerini I, Giorgio D, Virgili G, Rizzo S.

Ophthalmologica. 2019;242(4):195-207. doi: 10.1159/000501282. Epub 2019 Aug 15.

PMID:
31416074
4.

Optical Coherence Tomography Angiography (OCT-A) in young choroideremia (CHM) patients.

Murro V, Mucciolo DP, Giorgio D, Sodi A, Passerini I, Virgili G, Rizzo S.

Ophthalmic Genet. 2019 Jun;40(3):201-206. doi: 10.1080/13816810.2019.1611880. Epub 2019 May 28.

PMID:
31135252
5.

Multimodal imaging of benign yellow dot maculopathy.

Murro V, Mucciolo DP, Giorgio D, Sodi A, Passerini I, Pacini B, Finocchio L, Virgili G, Rizzo S.

Ophthalmic Genet. 2019 Apr;40(2):135-140. doi: 10.1080/13816810.2019.1589529. Epub 2019 Apr 3.

PMID:
30942106
6.

OCTA Imaging of Choroidal Neovascularization Treated Using Photodynamic Therapy in a Young Patient With Best Macular Dystrophy.

Murro V, Mucciolo DP, Giorgio D, Sodi A, Passerini I, Virgili G, Rizzo S.

Ophthalmic Surg Lasers Imaging Retina. 2018 Dec 1;49(12):969-973. doi: 10.3928/23258160-20181203-10.

PMID:
30566705
7.

Novel clinical findings in autosomal recessive NR2E3-related retinal dystrophy.

Murro V, Mucciolo DP, Sodi A, Passerini I, Giorgio D, Virgili G, Rizzo S.

Graefes Arch Clin Exp Ophthalmol. 2019 Jan;257(1):9-22. doi: 10.1007/s00417-018-4161-z. Epub 2018 Oct 15.

PMID:
30324420
8.

CFH Y402H polymorphism in Italian patients with age-related macular degeneration, retinitis pigmentosa, and Stargardt disease.

Sodi A, Passerini I, Bacherini D, Boni L, Palchetti S, Murro V, Caporossi O, Mucciolo DP, Franco F, Vannozzi L, Torricelli F, Pelo E, Rizzo S, Virgili G.

Ophthalmic Genet. 2018 Dec;39(6):699-705. doi: 10.1080/13816810.2018.1525753. Epub 2018 Oct 4.

PMID:
30285522
9.

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.

Ophthalmic Genet. 2018 Oct;39(5):589-602. doi: 10.1080/13816810.2018.1509351. Epub 2018 Aug 28.

PMID:
30153090
10.

Long-term follow-up of a CRB1-associated maculopathy.

Mucciolo DP, Murro V, Giorgio D, Passerini I, Sodi A, Virgili G, Rizzo S.

Ophthalmic Genet. 2018 Aug;39(4):522-525. doi: 10.1080/13816810.2018.1479431. Epub 2018 Jun 5.

PMID:
29869924
11.

EDI OCT evaluation of choroidal thickness in Stargardt disease.

Sodi A, Bacherini D, Lenzetti C, Caporossi O, Murro V, Mucciolo DP, Cipollini F, Passerini I, Virgili G, Rizzo S.

PLoS One. 2018 Jan 5;13(1):e0190780. doi: 10.1371/journal.pone.0190780. eCollection 2018.

12.

Targeted next generation sequencing in Italian patients with Usher syndrome: phenotype-genotype correlations.

Eandi CM, Dallorto L, Spinetta R, Micieli MP, Vanzetti M, Mariottini A, Passerini I, Torricelli F, Alovisi C, Marchese C.

Sci Rep. 2017 Nov 15;7(1):15681. doi: 10.1038/s41598-017-16014-z.

13.

A Computational Approach From Gene to Structure Analysis of the Human ABCA4 Transporter Involved in Genetic Retinal Diseases.

Trezza A, Bernini A, Langella A, Ascher DB, Pires DEV, Sodi A, Passerini I, Pelo E, Rizzo S, Niccolai N, Spiga O.

Invest Ophthalmol Vis Sci. 2017 Oct 1;58(12):5320-5328. doi: 10.1167/iovs.17-22158.

PMID:
29049734
14.

Retinal dystrophy and subretinal drusenoid deposits in female choroideremia carriers.

Murro V, Mucciolo DP, Passerini I, Palchetti S, Sodi A, Virgili G, Rizzo S.

Graefes Arch Clin Exp Ophthalmol. 2017 Nov;255(11):2099-2111. doi: 10.1007/s00417-017-3751-5. Epub 2017 Jul 27.

PMID:
28752371
15.

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.

Eur J Ophthalmol. 2018 Jan;28(1):52-57. doi: 10.5301/ejo.5000961.

PMID:
28604982
16.

A novel GRK1 mutation in an Italian patient with Oguchi disease.

Mucciolo DP, Sodi A, Murro V, Passerini I, Palchetti S, Pelo E, Virgili G, Rizzo S.

Ophthalmic Genet. 2018 Jan-Feb;39(1):137-138. doi: 10.1080/13816810.2017.1323341. Epub 2017 May 16. No abstract available.

PMID:
28511019
17.

Multimodal analysis of the Preferred Retinal Location and the Transition Zone in patients with Stargardt Disease.

Verdina T, Greenstein VC, Sodi A, Tsang SH, Burke TR, Passerini I, Allikmets R, Virgili G, Cavallini GM, Rizzo S.

Graefes Arch Clin Exp Ophthalmol. 2017 Jul;255(7):1307-1317. doi: 10.1007/s00417-017-3637-6. Epub 2017 Apr 2.

18.

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.

Ophthalmic Genet. 2015 Jun;36(2):168-74. doi: 10.3109/13816810.2015.1009121. Epub 2015 Feb 12.

PMID:
25675349
19.

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.

Mol Vis. 2014 Dec 23;20:1717-31. eCollection 2014.

20.

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.

Eur J Ophthalmol. 2014 Sep-Oct;24(5):814-7. doi: 10.5301/ejo.5000458. Epub 2014 Feb 24.

PMID:
24585425
21.

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.

Mol Vis. 2012;18:2736-48. Epub 2012 Nov 17.

22.

Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy.

Testa F, Rossi S, Sodi A, Passerini I, Di Iorio V, Della Corte M, Banfi S, Surace EM, Menchini U, Auricchio A, Simonelli F.

Invest Ophthalmol Vis Sci. 2012 Jul 3;53(8):4409-15. doi: 10.1167/iovs.11-8201.

23.

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.

Mol Vis. 2011;17:3078-87. Epub 2011 Nov 24.

24.

Novel RDH12 sequence variations in Leber congenital amaurosis.

Sodi A, Caputo R, Passerini I, Bacci GM, Menchini U.

J AAPOS. 2010 Aug;14(4):349-51. doi: 10.1016/j.jaapos.2010.04.010.

PMID:
20736127
25.

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.

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

PMID:
20128570
26.

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.

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

PMID:
19265867
27.

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.

Br J Ophthalmol. 2008 Nov;92(11):1467-70. doi: 10.1136/bjo.2008.143776. Epub 2008 Aug 14.

PMID:
18703557
28.

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.

Retin Cases Brief Rep. 2008 Winter;2(1):80-2. doi: 10.1097/01.iae.0000249397.40151.96.

PMID:
25389627
29.

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

Passerini I, Sodi A, Giambene B, Menchini U, Torricelli F.

Eur J Ophthalmol. 2007 Nov-Dec;17(6):1000-3.

PMID:
18050133
30.

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.

Clin Exp Ophthalmol. 2007 Nov;35(8):777-9.

PMID:
17997789
31.

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.

J Fr Ophtalmol. 2007 Jun;30(6):616-20.

PMID:
17646752
32.

A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy.

Girolami F, Olivotto I, Passerini I, Zachara E, Nistri S, Re F, Fantini S, Baldini K, Torricelli F, Cecchi F.

J Cardiovasc Med (Hagerstown). 2006 Aug;7(8):601-7.

PMID:
16858239
33.

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

Sodi A, Bini A, Passerini I, Menchini U, Torricelli F.

Eur J Ophthalmol. 2006 Mar-Apr;16(2):335-8.

PMID:
16703556
34.

Prevalence and clinical profile of troponin T mutations among patients with hypertrophic cardiomyopathy in tuscany.

Torricelli F, Girolami F, Olivotto I, Passerini I, Frusconi S, Vargiu D, Richard P, Cecchi F.

Am J Cardiol. 2003 Dec 1;92(11):1358-62.

PMID:
14636924
35.

Microsatellite analysis of chromosome 3p region in sporadic renal cell carcinomas.

Girolami F, Passerini I, Gargano D, Frusconi S, Villari D, Nicita G, Torricelli F.

Pathol Oncol Res. 2002;8(4):241-4. Epub 2003 Feb 11.

36.

Identification of seven novel mutations of F8C by DHPLC.

Frusconi S, Passerini I, Girolami F, Masieri M, Linari S, Longo G, Morfini M, Torricelli F.

Hum Mutat. 2002 Sep;20(3):231-2.

PMID:
12203998
37.

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

Marziliano N, Pelo E, Minuti B, Passerini I, Torricelli F, Da Prato L.

Clin Chem. 2000 Mar;46(3):423-5. No abstract available.

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