Benn M - Search Results

1

QT dispersion in patients with arrhythmogenic right ventricular dysplasia.

Benn M, Hansen PS, Pedersen AK. Benn M, et al. Eur Heart J. 1999 May;20(10):764-70. doi: 10.1053/euhj.1998.1400. Eur Heart J. 1999. PMID: 10329068

2

[Arrhythmogenic right ventricular cardiomyopathy].

Benn M, Hansen PS, Lund B, Schiønning JD, Baandrup U, Pedersen AK. Benn M, et al. Ugeskr Laeger. 1998 Mar 2;160(10):1454-9. Ugeskr Laeger. 1998. PMID: 9520612 Review. Danish.

3

[Hereditary long QT syndrome].

Lund B, Hansen PS, Benn M, Pedersen AK. Lund B, et al. Among authors: benn m. Ugeskr Laeger. 1998 Jun 8;160(24):3533-9. Ugeskr Laeger. 1998. PMID: 9641038 Review. Danish.

4

A reply.

Pedersen AK, Hansen PS, Benn M. Pedersen AK, et al. Among authors: benn m. Eur Heart J. 2000 Jan 1;21(1):79-80. doi: 10.1053/euhj.1999.1848. Eur Heart J. 2000. PMID: 10610748 No abstract available.

5

Missense variants in plakophilin-2 in arrhythmogenic right ventricular cardiomyopathy patients--disease-causing or innocent bystanders?

Christensen AH, Benn M, Tybjaerg-Hansen A, Haunso S, Svendsen JH. Christensen AH, et al. Among authors: benn m. Cardiology. 2010;115(2):148-54. doi: 10.1159/000263456. Epub 2009 Dec 3. Cardiology. 2010. PMID: 19955750 Free article.

6

Wide spectrum of desmosomal mutations in Danish patients with arrhythmogenic right ventricular cardiomyopathy.

Christensen AH, Benn M, Bundgaard H, Tybjaerg-Hansen A, Haunso S, Svendsen JH. Christensen AH, et al. Among authors: benn m. J Med Genet. 2010 Nov;47(11):736-44. doi: 10.1136/jmg.2010.077891. Epub 2010 Sep 23. J Med Genet. 2010. PMID: 20864495

7

Screening of three novel candidate genes in arrhythmogenic right ventricular cardiomyopathy.

Christensen AH, Benn M, Tybjærg-Hansen A, Haunso S, Svendsen JH. Christensen AH, et al. Among authors: benn m. Genet Test Mol Biomarkers. 2011 Apr;15(4):267-71. doi: 10.1089/gtmb.2010.0151. Epub 2011 Jan 22. Genet Test Mol Biomarkers. 2011. PMID: 21254927

8

Antihypertensive treatment and risk of atrial fibrillation: a nationwide study.

Marott SC, Nielsen SF, Benn M, Nordestgaard BG. Marott SC, et al. Among authors: benn m. Eur Heart J. 2014 May;35(18):1205-14. doi: 10.1093/eurheartj/eht507. Epub 2013 Dec 17. Eur Heart J. 2014. PMID: 24347316

9

Mutations causative of familial hypercholesterolaemia: screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217.

Benn M, Watts GF, Tybjærg-Hansen A, Nordestgaard BG. Benn M, et al. Eur Heart J. 2016 May 1;37(17):1384-94. doi: 10.1093/eurheartj/ehw028. Epub 2016 Feb 22. Eur Heart J. 2016. PMID: 26908947 Free article.

10

Genetic testing for familial hypercholesterolaemia is essential in individuals with high LDL cholesterol: who does it in the world?

Nordestgaard BG, Benn M. Nordestgaard BG, et al. Among authors: benn m. Eur Heart J. 2017 May 21;38(20):1580-1583. doi: 10.1093/eurheartj/ehx136. Eur Heart J. 2017. PMID: 28419271 No abstract available.

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