Ronchetti E - Search Results

1

Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.

Napolitano C, Priori SG, Schwartz PJ, Bloise R, Ronchetti E, Nastoli J, Bottelli G, Cerrone M, Leonardi S. Napolitano C, et al. Among authors: ronchetti e. JAMA. 2005 Dec 21;294(23):2975-80. doi: 10.1001/jama.294.23.2975. JAMA. 2005. PMID: 16414944

2

Natural history of Brugada syndrome: insights for risk stratification and management.

Priori SG, Napolitano C, Gasparini M, Pappone C, Della Bella P, Giordano U, Bloise R, Giustetto C, De Nardis R, Grillo M, Ronchetti E, Faggiano G, Nastoli J. Priori SG, et al. Among authors: ronchetti e. Circulation. 2002 Mar 19;105(11):1342-7. doi: 10.1161/hc1102.105288. Circulation. 2002. PMID: 11901046

3

Risk stratification in the long-QT syndrome.

Priori SG, Schwartz PJ, Napolitano C, Bloise R, Ronchetti E, Grillo M, Vicentini A, Spazzolini C, Nastoli J, Bottelli G, Folli R, Cappelletti D. Priori SG, et al. Among authors: ronchetti e. N Engl J Med. 2003 May 8;348(19):1866-74. doi: 10.1056/NEJMoa022147. N Engl J Med. 2003. PMID: 12736279 Free article.

4

Association of long QT syndrome loci and cardiac events among patients treated with beta-blockers.

Priori SG, Napolitano C, Schwartz PJ, Grillo M, Bloise R, Ronchetti E, Moncalvo C, Tulipani C, Veia A, Bottelli G, Nastoli J. Priori SG, et al. Among authors: ronchetti e. JAMA. 2004 Sep 15;292(11):1341-4. doi: 10.1001/jama.292.11.1341. JAMA. 2004. PMID: 15367556

5

A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.

Priori SG, Pandit SV, Rivolta I, Berenfeld O, Ronchetti E, Dhamoon A, Napolitano C, Anumonwo J, di Barletta MR, Gudapakkam S, Bosi G, Stramba-Badiale M, Jalife J. Priori SG, et al. Among authors: ronchetti e. Circ Res. 2005 Apr 15;96(7):800-7. doi: 10.1161/01.RES.0000162101.76263.8c. Epub 2005 Mar 10. Circ Res. 2005. PMID: 15761194

6

Evidence for a cardiac ion channel mutation underlying drug-induced QT prolongation and life-threatening arrhythmias.

Napolitano C, Schwartz PJ, Brown AM, Ronchetti E, Bianchi L, Pinnavaia A, Acquaro G, Priori SG. Napolitano C, et al. Among authors: ronchetti e. J Cardiovasc Electrophysiol. 2000 Jun;11(6):691-6. doi: 10.1111/j.1540-8167.2000.tb00033.x. J Cardiovasc Electrophysiol. 2000. PMID: 10868744

7

The elusive link between LQT3 and Brugada syndrome: the role of flecainide challenge.

Priori SG, Napolitano C, Schwartz PJ, Bloise R, Crotti L, Ronchetti E. Priori SG, et al. Among authors: ronchetti e. Circulation. 2000 Aug 29;102(9):945-7. doi: 10.1161/01.cir.102.9.945. Circulation. 2000. PMID: 10961955 Clinical Trial.

8

Cellular dysfunction of LQT5-minK mutants: abnormalities of IKs, IKr and trafficking in long QT syndrome.

Bianchi L, Shen Z, Dennis AT, Priori SG, Napolitano C, Ronchetti E, Bryskin R, Schwartz PJ, Brown AM. Bianchi L, et al. Among authors: ronchetti e. Hum Mol Genet. 1999 Aug;8(8):1499-507. doi: 10.1093/hmg/8.8.1499. Hum Mol Genet. 1999. PMID: 10400998

9

Gene specific therapy for arrhythmogenic disorders.

Priori SG, Ronchetti E, Memmi M. Priori SG, et al. Among authors: ronchetti e. Ital Heart J. 2000 Sep;1 Suppl 3:S52-4. Ital Heart J. 2000. PMID: 11003025 No abstract available.

10

Molecular diagnosis in a child with sudden infant death syndrome.

Schwartz PJ, Priori SG, Bloise R, Napolitano C, Ronchetti E, Piccinini A, Goj C, Breithardt G, Schulze-Bahr E, Wedekind H, Nastoli J. Schwartz PJ, et al. Among authors: ronchetti e. Lancet. 2001 Oct 20;358(9290):1342-3. doi: 10.1016/S0140-6736(01)06450-9. Lancet. 2001. PMID: 11684219

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