Bezzina CR - Search Results

1

Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesis.

Hoorntje ET, Te Rijdt WP, James CA, Pilichou K, Basso C, Judge DP, Bezzina CR, van Tintelen JP. Hoorntje ET, et al. Among authors: bezzina cr. Cardiovasc Res. 2017 Oct 1;113(12):1521-1531. doi: 10.1093/cvr/cvx150. Cardiovasc Res. 2017. PMID: 28957532 Review.

2

A single Na(+) channel mutation causing both long-QT and Brugada syndromes.

Bezzina C, Veldkamp MW, van Den Berg MP, Postma AV, Rook MB, Viersma JW, van Langen IM, Tan-Sindhunata G, Bink-Boelkens MT, van Der Hout AH, Mannens MM, Wilde AA. Bezzina C, et al. Circ Res. 1999 Dec 3-17;85(12):1206-13. doi: 10.1161/01.res.85.12.1206. Circ Res. 1999. PMID: 10590249

3

Cardiac sodium channel and inherited arrhythmia syndromes.

Bezzina CR, Rook MB, Wilde AA. Bezzina CR, et al. Cardiovasc Res. 2001 Feb 1;49(2):257-71. doi: 10.1016/s0008-6363(00)00272-8. Cardiovasc Res. 2001. PMID: 11164836 Review. No abstract available.

4

Genetic control of sodium channel function.

Tan HL, Bezzina CR, Smits JP, Verkerk AO, Wilde AA. Tan HL, et al. Among authors: bezzina cr. Cardiovasc Res. 2003 Mar 15;57(4):961-73. doi: 10.1016/s0008-6363(02)00714-9. Cardiovasc Res. 2003. PMID: 12650874 Review.

5

A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics.

Groenewegen WA, Bezzina CR, van Tintelen JP, Hoorntje TM, Mannens MM, Wilde AA, Jongsma HJ, Rook MB. Groenewegen WA, et al. Among authors: bezzina cr. Cardiovasc Res. 2003 Mar 15;57(4):1072-8. doi: 10.1016/s0008-6363(02)00838-6. Cardiovasc Res. 2003. PMID: 12650885

6

Developmental aspects of long QT syndrome type 3 and Brugada syndrome on the basis of a single SCN5A mutation in childhood.

Beaufort-Krol GC, van den Berg MP, Wilde AA, van Tintelen JP, Viersma JW, Bezzina CR, Bink-Boelkens MT. Beaufort-Krol GC, et al. Among authors: bezzina cr. J Am Coll Cardiol. 2005 Jul 19;46(2):331-7. doi: 10.1016/j.jacc.2005.03.066. J Am Coll Cardiol. 2005. PMID: 16022964 Free article.

7

Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndrome.

Smits JP, Veldkamp MW, Bezzina CR, Bhuiyan ZA, Wedekind H, Schulze-Bahr E, Wilde AA. Smits JP, et al. Among authors: bezzina cr. Cardiovasc Res. 2005 Aug 15;67(3):459-66. doi: 10.1016/j.cardiores.2005.01.017. Cardiovasc Res. 2005. PMID: 16039271

8

Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome.

Verkerk AO, Wilders R, Schulze-Bahr E, Beekman L, Bhuiyan ZA, Bertrand J, Eckardt L, Lin D, Borggrefe M, Breithardt G, Mannens MM, Tan HL, Wilde AA, Bezzina CR. Verkerk AO, et al. Among authors: bezzina cr. Cardiovasc Res. 2005 Dec 1;68(3):441-53. doi: 10.1016/j.cardiores.2005.06.027. Epub 2005 Jul 25. Cardiovasc Res. 2005. PMID: 16043162

9

Characterization of a novel SCN5A mutation associated with Brugada syndrome reveals involvement of DIIIS4-S5 linker in slow inactivation.

Casini S, Tan HL, Bhuiyan ZA, Bezzina CR, Barnett P, Cerbai E, Mugelli A, Wilde AA, Veldkamp MW. Casini S, et al. Among authors: bezzina cr. Cardiovasc Res. 2007 Dec 1;76(3):418-29. doi: 10.1016/j.cardiores.2007.08.005. Epub 2007 Aug 22. Cardiovasc Res. 2007. PMID: 17854786

10

The primary arrhythmia syndromes: same mutation, different manifestations. Are we starting to understand why?

Scicluna BP, Wilde AA, Bezzina CR. Scicluna BP, et al. Among authors: bezzina cr. J Cardiovasc Electrophysiol. 2008 Apr;19(4):445-52. doi: 10.1111/j.1540-8167.2007.01073.x. Epub 2008 Feb 12. J Cardiovasc Electrophysiol. 2008. PMID: 18284507 Review.

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