Brancato R - Search Results

1

Apolipoprotein E polymorphisms in age-related macular degeneration in an Italian population.

Simonelli F, Margaglione M, Testa F, Cappucci G, Manitto MP, Brancato R, Rinaldi E. Simonelli F, et al. Among authors: brancato r. Ophthalmic Res. 2001 Nov-Dec;33(6):325-8. doi: 10.1159/000055688. Ophthalmic Res. 2001. PMID: 11721184

2

Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian population.

Simonelli F, Frisso G, Testa F, di Fiore R, Vitale DF, Manitto MP, Brancato R, Rinaldi E, Sacchetti L. Simonelli F, et al. Among authors: brancato r. Br J Ophthalmol. 2006 Sep;90(9):1142-5. doi: 10.1136/bjo.2006.096487. Epub 2006 Jun 14. Br J Ophthalmol. 2006. PMID: 16774956 Free PMC article.

3

Macular dysplasia and pigmented paravenous retino-choroidal atrophy.

Nucci P, Manitto MP, Piantanida A, Brancato R. Nucci P, et al. Among authors: brancato r. Ophthalmic Genet. 1994 Sep-Dec;15(3-4):161-4. doi: 10.3109/13816819409057844. Ophthalmic Genet. 1994. PMID: 7749671 Free article.

4

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: brancato r. 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.

5

Balanced translocation (t 2q; 10p) and ocular anomalies. A possible HOX gene defect.

Nucci P, Manitto MP, Faiella A, Boncinelli E, Brancato R. Nucci P, et al. Among authors: brancato r. Ophthalmic Genet. 1994 Sep-Dec;15(3-4):129-31. doi: 10.3109/13816819409057839. Ophthalmic Genet. 1994. PMID: 7749666

6

Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patients.

Fumagalli A, Ferrari M, Soriani N, Gessi A, Foglieni B, Martina E, Manitto MP, Brancato R, Dean M, Allikmets R, Cremonesi L. Fumagalli A, et al. Among authors: brancato r. Hum Genet. 2001 Sep;109(3):326-38. doi: 10.1007/s004390100583. Hum Genet. 2001. PMID: 11702214

7

Are microarrays useful in the screening of ABCA4 mutations in Italian patients affected by macular degenerations?

Stenirri S, Alaimo G, Manitto MP, Brancato R, Ferrari M, Cremonesi L. Stenirri S, et al. Among authors: brancato r. Clin Chem Lab Med. 2008;46(9):1250-5. doi: 10.1515/CCLM.2008.248. Clin Chem Lab Med. 2008. PMID: 18652558

8

Identification and characterization of C1orf36, a transcript highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa.

Lavorgna G, Lestingi M, Ziviello C, Testa F, Simonelli F, Manitto MP, Brancato R, Ferrari M, Rinaldi E, Ciccodicola A, Banfi S. Lavorgna G, et al. Among authors: brancato r. Biochem Biophys Res Commun. 2003 Aug 29;308(3):414-21. doi: 10.1016/s0006-291x(03)01410-4. Biochem Biophys Res Commun. 2003. PMID: 12914764

9

Neuron-specific enolase and embryology of the trabecular meshwork of the rat eye: an immunohistochemical study.

Nucci P, Tredici G, Manitto MP, Pizzini G, Brancato R. Nucci P, et al. Among authors: brancato r. Int J Biol Markers. 1992 Oct-Dec;7(4):253-5. doi: 10.1177/172460089200700410. Int J Biol Markers. 1992. PMID: 1491183

10

Denaturing HPLC profiling of the ABCA4 gene for reliable detection of allelic variations.

Stenirri S, Fermo I, Battistella S, Galbiati S, Soriani N, Paroni R, Manitto MP, Martina E, Brancato R, Allikmets R, Ferrari M, Cremonesi L. Stenirri S, et al. Among authors: brancato r. Clin Chem. 2004 Aug;50(8):1336-43. doi: 10.1373/clinchem.2004.033241. Epub 2004 Jun 10. Clin Chem. 2004. PMID: 15192030

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