Rampazzo A - Search Results

1

Follow-up with exercise test of effort-induced ventricular arrhythmias linked to ryanodine receptor type 2 gene mutations.

Steriotis AK, Nava A, Rampazzo A, Basso C, Thiene G, Daliento L, Folino AF, Rigato I, Mazzotti E, Beffagna G, Carturan E, Corrado D, Bauce B. Steriotis AK, et al. Among authors: rampazzo a. Am J Cardiol. 2012 Apr 1;109(7):1015-9. doi: 10.1016/j.amjcard.2011.11.033. Epub 2012 Jan 3. Am J Cardiol. 2012. PMID: 22221940 Free PMC article.

2

Genetics of arrhythmogenic right ventricular cardiomyopathy.

Danieli GA, Rampazzo A. Danieli GA, et al. Among authors: rampazzo a. Curr Opin Cardiol. 2002 May;17(3):218-21. doi: 10.1097/00001573-200205000-00002. Curr Opin Cardiol. 2002. PMID: 12015469 Review.

3

Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers.

Bauce B, Rampazzo A, Basso C, Bagattin A, Daliento L, Tiso N, Turrini P, Thiene G, Danieli GA, Nava A. Bauce B, et al. Among authors: rampazzo a. J Am Coll Cardiol. 2002 Jul 17;40(2):341-9. doi: 10.1016/s0735-1097(02)01946-0. J Am Coll Cardiol. 2002. PMID: 12106942 Free article.

4

Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy.

Rampazzo A, Nava A, Malacrida S, Beffagna G, Bauce B, Rossi V, Zimbello R, Simionati B, Basso C, Thiene G, Towbin JA, Danieli GA. Rampazzo A, et al. Am J Hum Genet. 2002 Nov;71(5):1200-6. doi: 10.1086/344208. Epub 2002 Oct 8. Am J Hum Genet. 2002. PMID: 12373648 Free PMC article.

5

Identification and characterization of heart-specific splicing of human neurexin 3 mRNA (NRXN3).

Occhi G, Rampazzo A, Beffagna G, Antonio Danieli G. Occhi G, et al. Among authors: rampazzo a. Biochem Biophys Res Commun. 2002 Oct 18;298(1):151-5. doi: 10.1016/s0006-291x(02)02403-8. Biochem Biophys Res Commun. 2002. PMID: 12379233

6

Arrhythmogenic right ventricular cardiomyopathy type 1 (ARVD1): confirmation of locus assignment and mutation screening of four candidate genes.

Rampazzo A, Beffagna G, Nava A, Occhi G, Bauce B, Noiato M, Basso C, Frigo G, Thiene G, Towbin J, Danieli GA. Rampazzo A, et al. Eur J Hum Genet. 2003 Jan;11(1):69-76. doi: 10.1038/sj.ejhg.5200914. Eur J Hum Genet. 2003. PMID: 12529708

7

Denaturing HPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmias.

Bagattin A, Veronese C, Bauce B, Wuyts W, Settimo L, Nava A, Rampazzo A, Danieli GA. Bagattin A, et al. Among authors: rampazzo a. Clin Chem. 2004 Jul;50(7):1148-55. doi: 10.1373/clinchem.2003.030734. Epub 2004 May 6. Clin Chem. 2004. PMID: 15131021 Free article.

8

TAIL1: an isthmin-like gene, containing type 1 thrombospondin-repeat and AMOP domain, mapped to ARVD1 critical region.

Rossi V, Beffagna G, Rampazzo A, Bauce B, Danieli GA. Rossi V, et al. Among authors: rampazzo a. Gene. 2004 Jun 23;335:101-8. doi: 10.1016/j.gene.2004.03.008. Gene. 2004. PMID: 15194193

9

Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1.

Beffagna G, Occhi G, Nava A, Vitiello L, Ditadi A, Basso C, Bauce B, Carraro G, Thiene G, Towbin JA, Danieli GA, Rampazzo A. Beffagna G, et al. Among authors: rampazzo a. Cardiovasc Res. 2005 Feb 1;65(2):366-73. doi: 10.1016/j.cardiores.2004.10.005. Cardiovasc Res. 2005. PMID: 15639475

10

Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations.

Bauce B, Basso C, Rampazzo A, Beffagna G, Daliento L, Frigo G, Malacrida S, Settimo L, Danieli G, Thiene G, Nava A. Bauce B, et al. Among authors: rampazzo a. Eur Heart J. 2005 Aug;26(16):1666-75. doi: 10.1093/eurheartj/ehi341. Epub 2005 Jun 7. Eur Heart J. 2005. PMID: 15941723

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