Salvatore F - Search Results

1

Genetic analysis in a family affected by sick sinus syndrome may reduce the sudden death risk in a young aspiring competitive athlete.

Detta N, Frisso G, Limongelli G, Marzullo M, Calabrò R, Salvatore F. Detta N, et al. Among authors: salvatore f. Int J Cardiol. 2014 Jan 1;170(3):e63-5. doi: 10.1016/j.ijcard.2013.11.013. Epub 2013 Nov 12. Int J Cardiol. 2014. PMID: 24295898 Free article. No abstract available.

2

Novel deletion at the M and P promoters of the human dystrophin gene associated with a Duchenne muscular dystrophy.

Frisso G, Sampaolo S, Pastore L, Carlomagno A, Calise RM, Di Iorio G, Salvatore F. Frisso G, et al. Among authors: salvatore f. Neuromuscul Disord. 2002 Jun;12(5):494-7. doi: 10.1016/s0960-8966(01)00323-6. Neuromuscul Disord. 2002. PMID: 12031623

3

Direct detection of exon deletions/duplications in female carriers of and male patients with Duchenne/Becker muscular dystrophy.

Frisso G, Carsana A, Tinto N, Calcagno G, Salvatore F, Sacchetti L. Frisso G, et al. Among authors: salvatore f. Clin Chem. 2004 Aug;50(8):1435-8. doi: 10.1373/clinchem.2004.033795. Clin Chem. 2004. PMID: 15277355 Free article. No abstract available.

4

A larger spectrum of intragenic short tandem repeats improves linkage analysis and localization of intragenic recombination detection in the dystrophin gene: an analysis of 93 families from southern Italy.

Carsana A, Frisso G, Tremolaterra MR, Ricci E, De Rasmo D, Salvatore F. Carsana A, et al. Among authors: salvatore f. J Mol Diagn. 2007 Feb;9(1):64-9. doi: 10.2353/jmoldx.2007.060056. J Mol Diagn. 2007. PMID: 17251337 Free PMC article.

5

Microbial diversity in natural whey cultures used for the production of Caciocavallo Silano PDO cheese.

Ercolini D, Frisso G, Mauriello G, Salvatore F, Coppola S. Ercolini D, et al. Among authors: salvatore f. Int J Food Microbiol. 2008 May 31;124(2):164-70. doi: 10.1016/j.ijfoodmicro.2008.03.007. Epub 2008 Mar 27. Int J Food Microbiol. 2008. PMID: 18455822

6

A 15-year molecular analysis of DMD/BMD: genetic features in a large cohort.

Carsana A, Frisso G, Intrieri M, Tremolaterra MR, Savarese G, Scapagnini G, Esposito G, Santoro L, Salvatore F. Carsana A, et al. Among authors: salvatore f. Front Biosci (Elite Ed). 2010 Jan 1;2(2):547-58. doi: 10.2741/e113. Front Biosci (Elite Ed). 2010. PMID: 20036901 Free article.

7

The first case of mitochondrial acetoacetyl-CoA thiolase deficiency identified by expanded newborn metabolic screening in Italy: the importance of an integrated diagnostic approach.

Catanzano F, Ombrone D, Di Stefano C, Rossi A, Nosari N, Scolamiero E, Tandurella I, Frisso G, Parenti G, Ruoppolo M, Andria G, Salvatore F. Catanzano F, et al. Among authors: salvatore f. J Inherit Metab Dis. 2010 Dec;33 Suppl 3(Suppl 3):S91-4. doi: 10.1007/s10545-009-9028-3. Epub 2010 Feb 16. J Inherit Metab Dis. 2010. PMID: 20157782 Free PMC article.

8

Efficacy of pharmacological treatment and genetic characterization in early diagnosed patients affected by long QT syndrome with impaired AV conduction.

Sarubbi B, Frisso G, Romeo E, Evangelista E, Cordella A, D'Alto M, Santarpia G, Russo MG, Salvatore F, Calabrò R. Sarubbi B, et al. Among authors: salvatore f. Int J Cardiol. 2011 May 19;149(1):109-13. doi: 10.1016/j.ijcard.2010.12.099. Epub 2011 Apr 9. Int J Cardiol. 2011. PMID: 21481956 No abstract available.

9

Novel deletion mutation in the cardiac sodium channel inactivation gate causes long QT syndrome.

Detta N, Frisso G, Zullo A, Sarubbi B, Cozzolino C, Romeo E, Wang DW, Calabrò R, Salvatore F, George AL Jr. Detta N, et al. Among authors: salvatore f. Int J Cardiol. 2013 May 10;165(2):362-5. doi: 10.1016/j.ijcard.2012.08.032. Epub 2012 Sep 12. Int J Cardiol. 2013. PMID: 22980924 Free PMC article. No abstract available.

10

DNA sequence capture and next-generation sequencing for the molecular diagnosis of genetic cardiomyopathies.

D'Argenio V, Frisso G, Precone V, Boccia A, Fienga A, Pacileo G, Limongelli G, Paolella G, Calabrò R, Salvatore F. D'Argenio V, et al. Among authors: salvatore f. J Mol Diagn. 2014 Jan;16(1):32-44. doi: 10.1016/j.jmoldx.2013.07.008. Epub 2013 Oct 31. J Mol Diagn. 2014. PMID: 24183960 Free article.

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