Simonelli F - Search Results

1

Kurtenbach A, Hahn G, Kernstock C, Hipp S, Zobor D, Stingl K, Kohl S, Bonnet C, Mohand-Saïd S, Sliesoraityte I, Sahel JA, Audo I, Fakin A, Hawlina M, Testa F, Simonelli F, Petit C, Zrenner E. Kurtenbach A, et al. Among authors: simonelli f. Curr Eye Res. 2018 Oct;43(10):1295-1301. doi: 10.1080/02713683.2018.1501804. Epub 2018 Jul 30. Curr Eye Res. 2018. PMID: 30012035

2

Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family.

Simonelli F, Testa F, Zernant J, Nesti A, Rossi S, Rinaldi E, Allikmets R. Simonelli F, et al. Ophthalmic Res. 2004 Mar-Apr;36(2):82-8. doi: 10.1159/000076886. Ophthalmic Res. 2004. PMID: 15017103

3

Genetics of diabetic retinopathy.

Simonelli F, Testa F, Bandello F. Simonelli F, et al. Semin Ophthalmol. 2001 Mar;16(1):41-51. doi: 10.1076/soph.16.1.41.4219. Semin Ophthalmol. 2001. PMID: 15487697 Review. No abstract available.

4

Genotype-phenotype correlation in Italian families with Stargardt disease.

Simonelli F, Testa F, Zernant J, Nesti A, Rossi S, Allikmets R, Rinaldi E. Simonelli F, et al. Ophthalmic Res. 2005 May-Jun;37(3):159-67. doi: 10.1159/000086073. Epub 2005 May 7. Ophthalmic Res. 2005. PMID: 15942264

5

Intrafamilial clinical heterogeneity associated with a novel mutation of the retinal degeneration slow/peripherin gene.

Simonelli F, Testa F, Marini V, Interlandi E, Rossi S, Pognuz DR, Virgili G, Garrè C, Bandello F. Simonelli F, et al. Ophthalmic Res. 2007;39(5):255-9. doi: 10.1159/000108118. Epub 2007 Sep 12. Ophthalmic Res. 2007. PMID: 17851265

6

An atypical form of Bietti crystalline dystrophy.

Rossi S, Testa F, Li A, Iorio VD, Zhang J, Gesualdo C, Corte MD, Chan CC, Fielding Hejtmancik J, Simonelli F. Rossi S, et al. Among authors: simonelli f. Ophthalmic Genet. 2011 Jun;32(2):118-21. doi: 10.3109/13816810.2011.559653. Epub 2011 Mar 8. Ophthalmic Genet. 2011. PMID: 21385027 Free PMC article.

7

Molecular epidemiology of Usher syndrome in Italy.

Vozzi D, Aaspõllu A, Athanasakis E, Berto A, Fabretto A, Licastro D, Külm M, Testa F, Trevisi P, Vahter M, Ziviello C, Martini A, Simonelli F, Banfi S, Gasparini P. Vozzi D, et al. Among authors: simonelli f. Mol Vis. 2011;17:1662-8. Epub 2011 Jun 22. Mol Vis. 2011. PMID: 21738395 Free PMC article.

8

The role of optical coherence tomography in an atypical case of oculocutaneous albinism: a case report.

Rossi S, Testa F, Gargiulo A, Di Iorio V, Pierri RB, D'Alterio FM, Corte MD, Surace E, Simonelli F. Rossi S, et al. Among authors: simonelli f. Case Rep Ophthalmol. 2012 Jan;3(1):113-7. doi: 10.1159/000337489. Epub 2012 Mar 27. Case Rep Ophthalmol. 2012. PMID: 22548044 Free PMC article.

9

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. Testa F, et al. Among authors: simonelli f. Invest Ophthalmol Vis Sci. 2012 Jul 3;53(8):4409-15. doi: 10.1167/iovs.11-8201. Invest Ophthalmol Vis Sci. 2012. PMID: 22661472 Free PMC article.

10

Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients.

Melillo P, Pecchia L, Testa F, Rossi S, Bennett J, Simonelli F. Melillo P, et al. Among authors: simonelli f. Biomed Eng Online. 2012 Jul 19;11:40. doi: 10.1186/1475-925X-11-40. Biomed Eng Online. 2012. PMID: 22812667 Free PMC article.

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