Banfi S - Search Results

1

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: banfi s. 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

2

Drosophila-related expressed sequences.

Banfi S, Borsani G, Bulfone A, Ballabio A. Banfi S, et al. Hum Mol Genet. 1997;6(10):1745-53. doi: 10.1093/hmg/6.10.1745. Hum Mol Genet. 1997. PMID: 9300667 Review.

3

Identification and characterization of AFG3L2, a novel paraplegin-related gene.

Banfi S, Bassi MT, Andolfi G, Marchitiello A, Zanotta S, Ballabio A, Casari G, Franco B. Banfi S, et al. Genomics. 1999 Jul 1;59(1):51-8. doi: 10.1006/geno.1999.5818. Genomics. 1999. PMID: 10395799

4

Identification and characterization of YME1L1, a novel paraplegin-related gene.

Coppola M, Pizzigoni A, Banfi S, Bassi MT, Casari G, Incerti B. Coppola M, et al. Among authors: banfi s. Genomics. 2000 May 15;66(1):48-54. doi: 10.1006/geno.2000.6136. Genomics. 2000. PMID: 10843804

5

Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa.

Conte I, Lestingi M, den Hollander A, Miano MG, Alfano G, Circolo D, Pugliese M, Testa F, Simonelli F, Rinaldi E, Baiget M, Banfi S, Ciccodicola A. Conte I, et al. Among authors: banfi s. Gene. 2002 Sep 4;297(1-2):33-8. doi: 10.1016/s0378-1119(02)00872-7. Gene. 2002. PMID: 12384283

6

Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerations.

Conte I, Lestingi M, den Hollander A, Alfano G, Ziviello C, Pugliese M, Circolo D, Caccioppoli C, Ciccodicola A, Banfi S. Conte I, et al. Among authors: banfi s. Eur J Hum Genet. 2003 Feb;11(2):155-62. doi: 10.1038/sj.ejhg.5200942. Eur J Hum Genet. 2003. PMID: 12634863

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: banfi s. 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

Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families.

Ziviello C, Simonelli F, Testa F, Anastasi M, Marzoli SB, Falsini B, Ghiglione D, Macaluso C, Manitto MP, Garrè C, Ciccodicola A, Rinaldi E, Banfi S. Ziviello C, et al. Among authors: banfi s. J Med Genet. 2005 Jul;42(7):e47. doi: 10.1136/jmg.2005.031682. J Med Genet. 2005. PMID: 15994872 Free PMC article.

9

Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene.

Testa F, Ziviello C, Rinaldi M, Rossi S, Di Iorio V, Interlandi E, Ciccodicola A, Banfi S, Simonelli F. Testa F, et al. Among authors: banfi s. Eur J Ophthalmol. 2006 Sep-Oct;16(5):779-81. doi: 10.1177/112067210601600524. Eur J Ophthalmol. 2006. PMID: 17061239

10

Clinical and molecular genetics of Leber's congenital amaurosis: a multicenter study of Italian patients.

Simonelli F, Ziviello C, Testa F, Rossi S, Fazzi E, Bianchi PE, Fossarello M, Signorini S, Bertone C, Galantuomo S, Brancati F, Valente EM, Ciccodicola A, Rinaldi E, Auricchio A, Banfi S. Simonelli F, et al. Among authors: banfi s. Invest Ophthalmol Vis Sci. 2007 Sep;48(9):4284-90. doi: 10.1167/iovs.07-0068. Invest Ophthalmol Vis Sci. 2007. PMID: 17724218

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