Nesti A - Search Results

1

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. Among authors: nesti a. Ophthalmic Res. 2004 Mar-Apr;36(2):82-8. doi: 10.1159/000076886. Ophthalmic Res. 2004. PMID: 15017103

2

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. Among authors: nesti a. Ophthalmic Res. 2005 May-Jun;37(3):159-67. doi: 10.1159/000086073. Epub 2005 May 7. Ophthalmic Res. 2005. PMID: 15942264

3

An Italian family affected by autosomal dominant microcephaly with chorioretinal degeneration.

Simonell F, Testa F, Nesti A, de Crecchio G, Bifani M, Cavaliere ML, Rinaldi E, Rinaldi MM. Simonell F, et al. Among authors: nesti a. J Pediatr Ophthalmol Strabismus. 2002 Sep-Oct;39(5):288-92. doi: 10.3928/0191-3913-20020901-09. J Pediatr Ophthalmol Strabismus. 2002. PMID: 12353901 Review.

4

Evaluation of Italian patients with leber congenital amaurosis due to AIPL1 mutations highlights the potential applicability of gene therapy.

Testa F, Surace EM, Rossi S, Marrocco E, Gargiulo A, Di Iorio V, Ziviello C, Nesti A, Fecarotta S, Bacci ML, Giunti M, Della Corte M, Banfi S, Auricchio A, Simonelli F. Testa F, et al. Among authors: nesti a. Invest Ophthalmol Vis Sci. 2011 Jul 29;52(8):5618-24. doi: 10.1167/iovs.10-6543. Invest Ophthalmol Vis Sci. 2011. PMID: 21474771

5

The decrease of free epsilon-amino groups in senile and diabetic cataracts.

Simonelli F, Cotticelli L, Iura A, Manna C, Nesti A, Rinaldi E, Auricchio G. Simonelli F, et al. Among authors: nesti a. Ophthalmic Res. 1990;22(3):160-5. doi: 10.1159/000267017. Ophthalmic Res. 1990. PMID: 2385432

6

Systemic human diseases as oxidative risk factors in cataractogenesis. I. Diabetes.

Costagliola C, Iuliano G, Menzione M, Nesti A, Simonelli F, Rinaldi E. Costagliola C, et al. Among authors: nesti a. Ophthalmic Res. 1988;20(5):308-16. doi: 10.1159/000266734. Ophthalmic Res. 1988. PMID: 3186203

7

Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families.

Simonelli F, Cennamo G, Ziviello C, Testa F, de Crecchio G, Nesti A, Manitto MP, Ciccodicola A, Banfi S, Brancato R, Rinaldi E. Simonelli F, et al. Among authors: nesti a. Br J Ophthalmol. 2003 Sep;87(9):1130-4. doi: 10.1136/bjo.87.9.1130. Br J Ophthalmol. 2003. PMID: 12928282 Free PMC article.

8

Carbonic anhydrase inhibitors in patients with X-linked retinoschisis: effects on macular morphology and function.

Testa F, Di Iorio V, Gallo B, Marchese M, Nesti A, De Rosa G, Melillo P, Simonelli F. Testa F, et al. Among authors: nesti a. Ophthalmic Genet. 2019 Jun;40(3):207-212. doi: 10.1080/13816810.2019.1616303. Epub 2019 May 31. Ophthalmic Genet. 2019. PMID: 31149861

9

A novel mutation in the RDS gene in an Italian family with pattern dystrophy.

Testa F, Marini V, Rossi S, Interlandi E, Nesti A, Rinaldi M, Varano M, Garré C, Simonelli F. Testa F, et al. Among authors: nesti a. Br J Ophthalmol. 2005 Aug;89(8):1066-8. doi: 10.1136/bjo.2004.064188. Br J Ophthalmol. 2005. PMID: 16024869 Free PMC article. No abstract available.

10

Lipid peroxidation and human cataractogenesis in diabetes and severe myopia.

Simonelli F, Nesti A, Pensa M, Romano L, Savastano S, Rinaldi E, Auricchio G. Simonelli F, et al. Among authors: nesti a. Exp Eye Res. 1989 Aug;49(2):181-7. doi: 10.1016/0014-4835(89)90088-2. Exp Eye Res. 1989. PMID: 2767166

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