Hauer RNW - Search Results

1

Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features.

Ghidoni A, Elliott PM, Syrris P, Calkins H, James CA, Judge DP, Murray B, Barc J, Probst V, Schott JJ, Song JP, Hauer RNW, Hoorntje ET, van Tintelen JP, Schulze-Bahr E, Hamilton RM, Mittal K, Semsarian C, Behr ER, Ackerman MJ, Basso C, Parati G, Gentilini D, Kotta MC, Mayosi BM, Schwartz PJ, Crotti L. Ghidoni A, et al. Among authors: hauer rnw. Circ Genom Precis Med. 2021 Apr;14(2):e003097. doi: 10.1161/CIRCGEN.120.003097. Epub 2021 Feb 10. Circ Genom Precis Med. 2021. PMID: 33566628 Free PMC article.

2

Genetic and molecular basis of cardiac arrhythmias: impact on clinical management parts I and II.

Priori SG, Barhanin J, Hauer RN, Haverkamp W, Jongsma HJ, Kleber AG, McKenna WJ, Roden DM, Rudy Y, Schwartz K, Schwartz PJ, Towbin JA, Wilde AM. Priori SG, et al. Circulation. 1999 Feb 2;99(4):518-28. doi: 10.1161/01.cir.99.4.518. Circulation. 1999. PMID: 9927398 Review.

3

Genetic and molecular basis of cardiac arrhythmias: impact on clinical management part III.

Priori SG, Barhanin J, Hauer RN, Haverkamp W, Jongsma HJ, Kleber AG, McKenna WJ, Roden DM, Rudy Y, Schwartz K, Schwartz PJ, Towbin JA, Wilde AM. Priori SG, et al. Circulation. 1999 Feb 9;99(5):674-81. doi: 10.1161/01.cir.99.5.674. Circulation. 1999. PMID: 9950666 Review. No abstract available.

4

Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1).

Wilde AA, Jongbloed RJ, Doevendans PA, Düren DR, Hauer RN, van Langen IM, van Tintelen JP, Smeets HJ, Meyer H, Geelen JL. Wilde AA, et al. J Am Coll Cardiol. 1999 Feb;33(2):327-32. doi: 10.1016/s0735-1097(98)00578-6. J Am Coll Cardiol. 1999. PMID: 9973011 Free article.

5

[Presymptomatic screening after a sudden cardiac death in the family].

Wilde AA, van Langen IM, van Tintelen JP, Hauer RN. Wilde AA, et al. Ned Tijdschr Geneeskd. 1999 Aug 7;143(32):1643-8. Ned Tijdschr Geneeskd. 1999. PMID: 10494298 Review. Dutch.

6

Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy.

van Tintelen JP, Entius MM, Bhuiyan ZA, Jongbloed R, Wiesfeld AC, Wilde AA, van der Smagt J, Boven LG, Mannens MM, van Langen IM, Hofstra RM, Otterspoor LC, Doevendans PA, Rodriguez LM, van Gelder IC, Hauer RN. van Tintelen JP, et al. Circulation. 2006 Apr 4;113(13):1650-8. doi: 10.1161/CIRCULATIONAHA.105.609719. Epub 2006 Mar 27. Circulation. 2006. PMID: 16567567

7

Molecular genetics of arrhythmogenic right ventricular cardiomyopathy: emerging horizon?

van Tintelen JP, Hofstra RM, Wiesfeld AC, van den Berg MP, Hauer RN, Jongbloed JD. van Tintelen JP, et al. Curr Opin Cardiol. 2007 May;22(3):185-92. doi: 10.1097/HCO.0b013e3280d942c4. Curr Opin Cardiol. 2007. PMID: 17413274 Review.

8

Activation delay and VT parameters in arrhythmogenic right ventricular dysplasia/cardiomyopathy: toward improvement of diagnostic ECG criteria.

Cox MG, Nelen MR, Wilde AA, Wiesfeld AC, van der Smagt JJ, Loh P, Cramer MJ, Doevendans PA, van Tintelen JP, de Bakker JM, Hauer RN. Cox MG, et al. J Cardiovasc Electrophysiol. 2008 Aug;19(8):775-81. doi: 10.1111/j.1540-8167.2008.01140.x. Epub 2008 Mar 26. J Cardiovasc Electrophysiol. 2008. PMID: 18373594

9

Sarcoid myocarditis with ventricular tachycardia mimicking ARVD/C.

Ladyjanskaia GA, Basso C, Hobbelink MG, Kirkels JH, Lahpor JR, Cramer MJ, Thiene G, Hauer RN, V Oosterhout MF. Ladyjanskaia GA, et al. J Cardiovasc Electrophysiol. 2010 Jan;21(1):94-8. doi: 10.1111/j.1540-8167.2009.01479.x. Epub 2009 May 15. J Cardiovasc Electrophysiol. 2010. PMID: 19473301

10

Cardiomyopathies: New test for arrhythmogenic right ventricular cardiomyopathy.

van Tintelen JP, Hauer RN. van Tintelen JP, et al. Nat Rev Cardiol. 2009 Jul;6(7):450-1. doi: 10.1038/nrcardio.2009.97. Nat Rev Cardiol. 2009. PMID: 19554004

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