Torricelli F - Search Results

1

Microsatellite analysis of chromosome 3p region in sporadic renal cell carcinomas.

Girolami F, Passerini I, Gargano D, Frusconi S, Villari D, Nicita G, Torricelli F. Girolami F, et al. Among authors: torricelli f. Pathol Oncol Res. 2002;8(4):241-4. doi: 10.1007/BF03036738. Epub 2003 Feb 11. Pathol Oncol Res. 2002. PMID: 12579209 Free article.

2

Identification of seven novel mutations of F8C by DHPLC.

Frusconi S, Passerini I, Girolami F, Masieri M, Linari S, Longo G, Morfini M, Torricelli F. Frusconi S, et al. Among authors: torricelli f. Hum Mutat. 2002 Sep;20(3):231-2. doi: 10.1002/humu.9052. Hum Mutat. 2002. PMID: 12203998

3

Prevalence and clinical profile of troponin T mutations among patients with hypertrophic cardiomyopathy in tuscany.

Torricelli F, Girolami F, Olivotto I, Passerini I, Frusconi S, Vargiu D, Richard P, Cecchi F. Torricelli F, et al. Am J Cardiol. 2003 Dec 1;92(11):1358-62. doi: 10.1016/j.amjcard.2003.08.031. Am J Cardiol. 2003. PMID: 14636924

4

A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy.

Girolami F, Olivotto I, Passerini I, Zachara E, Nistri S, Re F, Fantini S, Baldini K, Torricelli F, Cecchi F. Girolami F, et al. Among authors: torricelli f. J Cardiovasc Med (Hagerstown). 2006 Aug;7(8):601-7. doi: 10.2459/01.JCM.0000237908.26377.d6. J Cardiovasc Med (Hagerstown). 2006. PMID: 16858239

5

A new ATTR Phe64Ile mutation with late-onset multiorgan involvement.

Tarquini R, Perfetto F, Bergesio F, Miliani A, Del Pace S, Frusconi S, Minuti B, Pelo E, Torricelli F. Tarquini R, et al. Among authors: torricelli f. Amyloid. 2007 Dec;14(4):289-92. doi: 10.1080/13506120701614172. Amyloid. 2007. PMID: 17968689

6

Improvement of low-density microelectronic array technology to characterize 14 mutations/single-nucleotide polymorphisms from several human genes on a large scale.

Frusconi S, Giusti B, Rossi L, Bernabini S, Poggi F, Giotti I, Abbate R, Pepe G, Torricelli F. Frusconi S, et al. Among authors: torricelli f. Clin Chem. 2004 Apr;50(4):775-7. doi: 10.1373/clinchem.2003.025197. Clin Chem. 2004. PMID: 15044341 No abstract available.

7

Bioinformatics for next generation sequencing data.

Magi A, Benelli M, Gozzini A, Girolami F, Torricelli F, Brandi ML. Magi A, et al. Among authors: torricelli f. Genes (Basel). 2010 Sep 14;1(2):294-307. doi: 10.3390/genes1020294. Genes (Basel). 2010. PMID: 24710047 Free PMC article.

8

Variable expressivity of abca4 gene mutations in an italian family with stargardt disease.

Sodi A, Bini A, Passerini I, Puccioni M, Torricelli F, Menchini U. Sodi A, et al. Among authors: torricelli f. Retin Cases Brief Rep. 2008 Winter;2(1):80-2. doi: 10.1097/01.iae.0000249397.40151.96. Retin Cases Brief Rep. 2008. PMID: 25389627

9

MYO7A and USH2A gene sequence variants in Italian patients with Usher syndrome.

Sodi A, Mariottini A, Passerini I, Murro V, Tachyla I, Bianchi B, Menchini U, Torricelli F. Sodi A, et al. Among authors: torricelli f. Mol Vis. 2014 Dec 23;20:1717-31. eCollection 2014. Mol Vis. 2014. PMID: 25558175 Free PMC article.

10

Relevance of coronary microvascular flow impairment to long-term remodeling and systolic dysfunction in hypertrophic cardiomyopathy.

Olivotto I, Cecchi F, Gistri R, Lorenzoni R, Chiriatti G, Girolami F, Torricelli F, Camici PG. Olivotto I, et al. Among authors: torricelli f. J Am Coll Cardiol. 2006 Mar 7;47(5):1043-8. doi: 10.1016/j.jacc.2005.10.050. J Am Coll Cardiol. 2006. PMID: 16516091 Free article.

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