Stenirri S - Search Results

1

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. Clin Chem Lab Med. 2008;46(9):1250-5. doi: 10.1515/CCLM.2008.248. Clin Chem Lab Med. 2008. PMID: 18652558

2

Molecular diagnostics by microelectronic microchips.

Ferrari M, Stenirri S, Bonini P, Cremonesi L. Ferrari M, et al. Among authors: stenirri s. Clin Chem Lab Med. 2003 Apr;41(4):462-7. doi: 10.1515/CCLM.2003.069. Clin Chem Lab Med. 2003. PMID: 12747587 Review.

3

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. Clin Chem. 2004 Aug;50(8):1336-43. doi: 10.1373/clinchem.2004.033241. Epub 2004 Jun 10. Clin Chem. 2004. PMID: 15192030

4

De novo deletion removes a conserved motif in the C-terminus of ABCA4 and results in cone-rod dystrophy.

Stenirri S, Battistella S, Fermo I, Manitto MP, Martina E, Brancato R, Ferrari M, Cremonesi L. Stenirri S, et al. Clin Chem Lab Med. 2006;44(5):533-7. doi: 10.1515/CCLM.2006.116. Clin Chem Lab Med. 2006. PMID: 16681420

5

Integrated strategy for fast and automated molecular characterization of genes involved in craniosynostosis.

Stenirri S, Restagno G, Ferrero GB, Alaimo G, Sbaiz L, Mari C, Genitori L, Maurizio F, Cremonesi L. Stenirri S, et al. Clin Chem. 2007 Oct;53(10):1767-74. doi: 10.1373/clinchem.2007.089292. Epub 2007 Aug 10. Clin Chem. 2007. PMID: 17693524

6

Study of FTMT and ABCA4 genes in a patient affected by age-related macular degeneration: identification and analysis of new mutations.

Stenirri S, Santambrogio P, Setaccioli M, Erba BG, Pia Manitto M, Rovida E, Ferrari M, Levi S, Cremonesi L. Stenirri S, et al. Clin Chem Lab Med. 2012 Jan 9;50(6):1021-9. doi: 10.1515/cclm-2011-0854. Clin Chem Lab Med. 2012. PMID: 22706241

7

Molecular scanning of the ABCA4 gene in Spanish patients with retinitis pigmentosa and Stargardt disease: identification of novel mutations.

Stenirri S, Battistella S, Soriani N, Bernal S, Baiget M, Ferrari M, Cremonesi L. Stenirri S, et al. Eur J Ophthalmol. 2007 Sep-Oct;17(5):749-54. doi: 10.1177/112067210701700510. Eur J Ophthalmol. 2007. PMID: 17932850

8

Denaturing HPLC analysis of DNA deletions and insertions.

Cremonesi L, Stenirri S, Fermo I, Paroni R, Ferrari M, Cazzola M, Arosio P. Cremonesi L, et al. Among authors: stenirri s. Hum Mutat. 2003 Jul;22(1):98-102. doi: 10.1002/humu.10234. Hum Mutat. 2003. PMID: 12815600

9

Molecular diagnostics by microelectronic microchips.

Ferrari M, Cremonesi L, Bonini P, Stenirri S, Foglieni B. Ferrari M, et al. Among authors: stenirri s. Expert Rev Mol Diagn. 2005 Mar;5(2):183-92. doi: 10.1586/14737159.5.2.183. Expert Rev Mol Diagn. 2005. PMID: 15833048 Review.

10

Single-nucleotide polymorphism and mutation identification by the nanogen microelectronic chip technology.

Ferrari M, Cremonesi L, Bonini P, Foglieni B, Stenirri S. Ferrari M, et al. Among authors: stenirri s. Methods Mol Med. 2005;114:93-106. doi: 10.1385/1-59259-923-0:93. Methods Mol Med. 2005. PMID: 16156099

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