Lucarelli M - Search Results

1

Genotype-phenotype correlation and functional studies in patients with cystic fibrosis bearing CFTR complex alleles.

Terlizzi V, Castaldo G, Salvatore D, Lucarelli M, Raia V, Angioni A, Carnovale V, Cirilli N, Casciaro R, Colombo C, Di Lullo AM, Elce A, Iacotucci P, Comegna M, Scorza M, Lucidi V, Perfetti A, Cimino R, Quattrucci S, Seia M, Sofia VM, Zarrilli F, Amato F. Terlizzi V, et al. Among authors: lucarelli m. J Med Genet. 2017 Apr;54(4):224-235. doi: 10.1136/jmedgenet-2016-103985. Epub 2016 Oct 13. J Med Genet. 2017. PMID: 27738188 Free article.

2

Simultaneous cycle sequencing assessment of (TG)m and Tn tract length in CFTR gene.

Lucarelli M, Grandoni F, Rossi T, Mazzilli F, Antonelli M, Strom R. Lucarelli M, et al. Biotechniques. 2002 Mar;32(3):540-2, 544-7. doi: 10.2144/02323st06. Biotechniques. 2002. PMID: 11911657 Free article.

3

Comparison of two different protocols of neonatal screening for cystic fibrosis.

Narzi L, Lucarelli M, Lelli A, Grandoni F, Lo Cicero S, Ferraro A, Matarazzo P, Delaroche I, Quattrucci S, Strom R, Antonelli M. Narzi L, et al. Among authors: lucarelli m. Clin Genet. 2002 Sep;62(3):245-9. doi: 10.1034/j.1399-0004.2002.620311.x. Clin Genet. 2002. PMID: 12220442

4

High frequency of (TG)mTn variant tracts in the cystic fibrosis transmembrane conductance regulator gene in men with high semen viscosity.

Rossi T, Grandoni F, Mazzilli F, Quattrucci S, Antonelli M, Strom R, Lucarelli M. Rossi T, et al. Among authors: lucarelli m. Fertil Steril. 2004 Nov;82(5):1316-22. doi: 10.1016/j.fertnstert.2004.03.065. Fertil Steril. 2004. PMID: 15533353 Free article.

5

A 96-well formatted method for exon and exon/intron boundary full sequencing of the CFTR gene.

Lucarelli M, Narzi L, Piergentili R, Ferraguti G, Grandoni F, Quattrucci S, Strom R. Lucarelli M, et al. Anal Biochem. 2006 Jun 15;353(2):226-35. doi: 10.1016/j.ab.2006.03.022. Epub 2006 Apr 5. Anal Biochem. 2006. PMID: 16635477

6

Does cystic fibrosis neonatal screening detect atypical CF forms? Extended genetic characterization and 4-year clinical follow-up.

Narzi L, Ferraguti G, Stamato A, Narzi F, Valentini SB, Lelli A, Delaroche I, Lucarelli M, Strom R, Quattrucci S. Narzi L, et al. Among authors: lucarelli m. Clin Genet. 2007 Jul;72(1):39-46. doi: 10.1111/j.1399-0004.2007.00825.x. Clin Genet. 2007. PMID: 17594398

7

A new complex allele of the CFTR gene partially explains the variable phenotype of the L997F mutation.

Lucarelli M, Narzi L, Pierandrei S, Bruno SM, Stamato A, d'Avanzo M, Strom R, Quattrucci S. Lucarelli M, et al. Genet Med. 2010 Sep;12(9):548-55. doi: 10.1097/GIM.0b013e3181ead634. Genet Med. 2010. PMID: 20706124 Free article.

8

A template for mutational data analysis of the CFTR gene.

Ferraguti G, Pierandrei S, Bruno SM, Ceci F, Strom R, Lucarelli M. Ferraguti G, et al. Among authors: lucarelli m. Clin Chem Lab Med. 2011 Sep;49(9):1447-51. doi: 10.1515/CCLM.2011.604. Epub 2011 May 31. Clin Chem Lab Med. 2011. PMID: 21627495 Free PMC article.

9

Cystic fibrosis transmembrane conductance regulator (CFTR) allelic variants relate to shifts in faecal microbiota of cystic fibrosis patients.

Schippa S, Iebba V, Santangelo F, Gagliardi A, De Biase RV, Stamato A, Bertasi S, Lucarelli M, Conte MP, Quattrucci S. Schippa S, et al. Among authors: lucarelli m. PLoS One. 2013 Apr 17;8(4):e61176. doi: 10.1371/journal.pone.0061176. Print 2013. PLoS One. 2013. PMID: 23613805 Free PMC article.

10

Clinical expression of patients with the D1152H CFTR mutation.

Terlizzi V, Carnovale V, Castaldo G, Castellani C, Cirilli N, Colombo C, Corti F, Cresta F, D'Adda A, Lucarelli M, Lucidi V, Macchiaroli A, Madarena E, Padoan R, Quattrucci S, Salvatore D, Zarrilli F, Raia V. Terlizzi V, et al. Among authors: lucarelli m. J Cyst Fibros. 2015 Jul;14(4):447-52. doi: 10.1016/j.jcf.2014.12.012. Epub 2015 Jan 10. J Cyst Fibros. 2015. PMID: 25583415 Free article.

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