Calabrò R - Search Results

1

Functional Studies and In Silico Analyses to Evaluate Non-Coding Variants in Inherited Cardiomyopathies.

Frisso G, Detta N, Coppola P, Mazzaccara C, Pricolo MR, D'Onofrio A, Limongelli G, Calabrò R, Salvatore F. Frisso G, et al. Among authors: calabro r. Int J Mol Sci. 2016 Nov 10;17(11):1883. doi: 10.3390/ijms17111883. Int J Mol Sci. 2016. PMID: 27834932 Free PMC article.

2

Allelic Complexity in Long QT Syndrome: A Family-Case Study.

Zullo A, Frisso G, Detta N, Sarubbi B, Romeo E, Cordella A, Vanoye CG, Calabrò R, George AL, Salvatore F. Zullo A, et al. Among authors: calabro r. Int J Mol Sci. 2017 Jul 27;18(8):1633. doi: 10.3390/ijms18081633. Int J Mol Sci. 2017. PMID: 28749435 Free PMC article.

3

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: calabro r. 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.

4

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: calabro r. 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.

5

A child cohort study from southern Italy enlarges the genetic spectrum of hypertrophic cardiomyopathy.

Frisso G, Limongelli G, Pacileo G, Del Giudice A, Forgione L, Calabrò P, Iacomino M, Detta N, Di Fonzo LM, Maddaloni V, Calabrò R, Salvatore F. Frisso G, et al. Among authors: calabro r, calabro p. Clin Genet. 2009 Jul;76(1):91-101. doi: 10.1111/j.1399-0004.2009.01190.x. Clin Genet. 2009. PMID: 19659763

6

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: calabro r. 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.

7

Clinical and genetic characterization of patients with hypertrophic cardiomyopathy and right atrial enlargement.

Limongelli G, Masarone D, Frisso G, Iacomino M, Ferrara I, Rea A, Gravino R, Bossone E, Salvatore F, Calabro R, Elliott P, Pacileo G. Limongelli G, et al. Among authors: calabro r. J Cardiovasc Med (Hagerstown). 2017 Apr;18(4):249-254. doi: 10.2459/JCM.0000000000000361. J Cardiovasc Med (Hagerstown). 2017. PMID: 26808413

8

Complete atrioventricular canal.

Calabrò R, Limongelli G. Calabrò R, et al. Orphanet J Rare Dis. 2006 Apr 5;1:8. doi: 10.1186/1750-1172-1-8. Orphanet J Rare Dis. 2006. PMID: 16722604 Free PMC article. Review.

9

Is sudden cardiac death predictable in LEOPARD syndrome?

Limongelli G, Pacileo G, Calabrò R. Limongelli G, et al. Among authors: calabro r. Cardiol Young. 2006 Dec;16(6):599-601. doi: 10.1017/S1047951106001247. Cardiol Young. 2006. PMID: 17116277

10

Right ventricular cardiomyopathies: a multidisciplinary approach to diagnosis.

Limongelli G, Rea A, Masarone D, Francalanci MP, Anastasakis A, Calabro' R, Giovanna RM, Bossone E, Elliott PM, Pacileo G. Limongelli G, et al. Among authors: calabro r. Echocardiography. 2015 Jan;32 Suppl 1:S75-94. doi: 10.1111/echo.12399. Epub 2014 Sep 19. Echocardiography. 2015. PMID: 25234203 Review.

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