Bezzina CR - Search Results

1

Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death.

Lahrouchi N, Lodder EM, Mansouri M, Tadros R, Zniber L, Adadi N, Clur SB, van Spaendonck-Zwarts KY, Postma AV, Sefiani A, Ratbi I, Bezzina CR. Lahrouchi N, et al. Among authors: bezzina cr. Eur J Hum Genet. 2017 Jun;25(6):783-787. doi: 10.1038/ejhg.2017.22. Epub 2017 Mar 15. Eur J Hum Genet. 2017. PMID: 28295041 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

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

4

Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation.

Alders M, Koopmann TT, Christiaans I, Postema PG, Beekman L, Tanck MW, Zeppenfeld K, Loh P, Koch KT, Demolombe S, Mannens MM, Bezzina CR, Wilde AA. Alders M, et al. Among authors: bezzina cr. Am J Hum Genet. 2009 Apr;84(4):468-76. doi: 10.1016/j.ajhg.2009.02.009. Epub 2009 Mar 12. Am J Hum Genet. 2009. PMID: 19285295 Free PMC article.

5

A complex double deletion in LMNA underlies progressive cardiac conduction disease, atrial arrhythmias, and sudden death.

Marsman RF, Bardai A, Postma AV, Res JC, Koopmann TT, Beekman L, van der Wal AC, Pinto YM, Lekanne Deprez RH, Wilde AA, Jordaens LJ, Bezzina CR. Marsman RF, et al. Among authors: bezzina cr. Circ Cardiovasc Genet. 2011 Jun;4(3):280-7. doi: 10.1161/CIRCGENETICS.110.959221. Epub 2011 Mar 15. Circ Cardiovasc Genet. 2011. PMID: 21406687

6

Developmental aspects of cardiac arrhythmogenesis.

Postma AV, Christoffels VM, Bezzina CR. Postma AV, et al. Among authors: bezzina cr. Cardiovasc Res. 2011 Jul 15;91(2):243-51. doi: 10.1093/cvr/cvr134. Epub 2011 May 12. Cardiovasc Res. 2011. PMID: 21565834 Review.

7

The role of renin-angiotensin-aldosterone system polymorphisms in phenotypic expression of MYBPC3-related hypertrophic cardiomyopathy.

Kolder IC, Michels M, Christiaans I, Ten Cate FJ, Majoor-Krakauer D, Danser AH, Lekanne Deprez RH, Tanck M, Wilde AA, Bezzina CR, Dooijes D. Kolder IC, et al. Among authors: bezzina cr. Eur J Hum Genet. 2012 Oct;20(10):1071-7. doi: 10.1038/ejhg.2012.48. Epub 2012 May 9. Eur J Hum Genet. 2012. PMID: 22569109 Free PMC article.

8

Dissection of a quantitative trait locus for PR interval duration identifies Tnni3k as a novel modulator of cardiac conduction.

Lodder EM, Scicluna BP, Milano A, Sun AY, Tang H, Remme CA, Moerland PD, Tanck MW, Pitt GS, Marchuk DA, Bezzina CR. Lodder EM, et al. Among authors: bezzina cr. PLoS Genet. 2012;8(12):e1003113. doi: 10.1371/journal.pgen.1003113. Epub 2012 Dec 6. PLoS Genet. 2012. PMID: 23236294 Free PMC article.

9

Genomics of cardiac electrical function.

Lodder EM, Bezzina CR. Lodder EM, et al. Among authors: bezzina cr. Brief Funct Genomics. 2014 Jan;13(1):39-50. doi: 10.1093/bfgp/elt029. Epub 2013 Aug 16. Brief Funct Genomics. 2014. PMID: 23956259 Review.

10

A mutation in CALM1 encoding calmodulin in familial idiopathic ventricular fibrillation in childhood and adolescence.

Marsman RF, Barc J, Beekman L, Alders M, Dooijes D, van den Wijngaard A, Ratbi I, Sefiani A, Bhuiyan ZA, Wilde AA, Bezzina CR. Marsman RF, et al. Among authors: bezzina cr. J Am Coll Cardiol. 2014 Jan 28;63(3):259-66. doi: 10.1016/j.jacc.2013.07.091. Epub 2013 Sep 25. J Am Coll Cardiol. 2014. PMID: 24076290 Free article.

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