Bezzina CR - Search Results

1

Two siblings with early repolarization syndrome: clinical and genetic characterization by whole-exome sequencing.

Steinfurt J, Bezzina CR, Biermann J, Staudacher D, Marschall C, Trolese L, Faber TS, Duerschmied D, Zehender M, Bode C, Wilde AAM, Odening KE, Lodder EM. Steinfurt J, et al. Among authors: bezzina cr. Europace. 2021 May 21;23(5):775-780. doi: 10.1093/europace/euaa357. Europace. 2021. PMID: 33324992 Free PMC article.

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

Two distinct congenital arrhythmias evoked by a multidysfunctional Na(+) channel.

Veldkamp MW, Viswanathan PC, Bezzina C, Baartscheer A, Wilde AA, Balser JR. Veldkamp MW, et al. Circ Res. 2000 May 12;86(9):E91-7. doi: 10.1161/01.res.86.9.e91. Circ Res. 2000. PMID: 10807877

4

Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3.

Postma AV, Bezzina CR, de Vries JF, Wilde AA, Moorman AF, Mannens MM. Postma AV, et al. Among authors: bezzina cr. Hum Genet. 2000 Jun;106(6):614-9. doi: 10.1007/s004390000308. Hum Genet. 2000. PMID: 10942109

5

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.

6

A sodium-channel mutation causes isolated cardiac conduction disease.

Tan HL, Bink-Boelkens MT, Bezzina CR, Viswanathan PC, Beaufort-Krol GC, van Tintelen PJ, van den Berg MP, Wilde AA, Balser JR. Tan HL, et al. Among authors: bezzina cr. Nature. 2001 Feb 22;409(6823):1043-7. doi: 10.1038/35059090. Nature. 2001. PMID: 11234013

7

Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients.

Smits JP, Eckardt L, Probst V, Bezzina CR, Schott JJ, Remme CA, Haverkamp W, Breithardt G, Escande D, Schulze-Bahr E, LeMarec H, Wilde AA. Smits JP, et al. Among authors: bezzina cr. J Am Coll Cardiol. 2002 Jul 17;40(2):350-6. doi: 10.1016/s0735-1097(02)01962-9. J Am Coll Cardiol. 2002. PMID: 12106943 Free article.

8

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill.

Groenewegen WA, Firouzi M, Bezzina CR, Vliex S, van Langen IM, Sandkuijl L, Smits JP, Hulsbeek M, Rook MB, Jongsma HJ, Wilde AA. Groenewegen WA, et al. Among authors: bezzina cr. Circ Res. 2003 Jan 10;92(1):14-22. doi: 10.1161/01.res.0000050585.07097.d7. Circ Res. 2003. PMID: 12522116

9

Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system.

Bezzina CR, Rook MB, Groenewegen WA, Herfst LJ, van der Wal AC, Lam J, Jongsma HJ, Wilde AA, Mannens MM. Bezzina CR, et al. Circ Res. 2003 Feb 7;92(2):159-68. doi: 10.1161/01.res.0000052672.97759.36. Circ Res. 2003. PMID: 12574143

10

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.

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