Hofman N - Search Results

1

Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6.

Postema PG, Christiaans I, Hofman N, Alders M, Koopmann TT, Bezzina CR, Loh P, Zeppenfeld K, Volders PG, Wilde AA. Postema PG, et al. Among authors: hofman n. Neth Heart J. 2011 Jun;19(6):290-6. doi: 10.1007/s12471-011-0102-8. Neth Heart J. 2011. PMID: 21512816 Free PMC article.

2

Family and population strategies for screening and counselling of inherited cardiac arrhythmias.

van Langen IM, Hofman N, Tan HL, Wilde AA. van Langen IM, et al. Among authors: hofman n. Ann Med. 2004;36 Suppl 1:116-24. doi: 10.1080/17431380410032526. Ann Med. 2004. PMID: 15176433 Free article.

3

Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives.

Tan HL, Hofman N, van Langen IM, van der Wal AC, Wilde AA. Tan HL, et al. Among authors: hofman n. Circulation. 2005 Jul 12;112(2):207-13. doi: 10.1161/CIRCULATIONAHA.104.522581. Epub 2005 Jul 5. Circulation. 2005. PMID: 15998675

4

Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey.

van Langen IM, Birnie E, Schuurman E, Tan HL, Hofman N, Bonsel GJ, Wilde AA. van Langen IM, et al. Among authors: hofman n. Clin Genet. 2005 Oct;68(4):360-8. doi: 10.1111/j.1399-0004.2005.00502.x. Clin Genet. 2005. PMID: 16143023

5

Diagnostic value of flecainide testing in unmasking SCN5A-related Brugada syndrome.

Meregalli PG, Ruijter JM, Hofman N, Bezzina CR, Wilde AA, Tan HL. Meregalli PG, et al. Among authors: hofman n. J Cardiovasc Electrophysiol. 2006 Aug;17(8):857-64. doi: 10.1111/j.1540-8167.2006.00531.x. Epub 2006 Jun 9. J Cardiovasc Electrophysiol. 2006. PMID: 16764707

6

Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?

Hofman N, Wilde AA, Kääb S, van Langen IM, Tanck MW, Mannens MM, Hinterseer M, Beckmann BM, Tan HL. Hofman N, et al. Eur Heart J. 2007 Mar;28(5):575-80. doi: 10.1093/eurheartj/ehl355. Epub 2006 Nov 7. Eur Heart J. 2007. PMID: 17090615

7

[Genetic identification of patients and families with a long-QT syndrome: large regional differences in the result of 10 years].

Hofman N, Postema PG, van Langen IM, Nannenberg EA, Alders M, Jongbloed R, Smeets HJ, Wilde AA. Hofman N, et al. Ned Tijdschr Geneeskd. 2007 Mar 17;151(11):644-8. Ned Tijdschr Geneeskd. 2007. PMID: 17441570 Dutch.

8

Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene.

Moss AJ, Shimizu W, Wilde AA, Towbin JA, Zareba W, Robinson JL, Qi M, Vincent GM, Ackerman MJ, Kaufman ES, Hofman N, Seth R, Kamakura S, Miyamoto Y, Goldenberg I, Andrews ML, McNitt S. Moss AJ, et al. Among authors: hofman n. Circulation. 2007 May 15;115(19):2481-9. doi: 10.1161/CIRCULATIONAHA.106.665406. Epub 2007 Apr 30. Circulation. 2007. PMID: 17470695 Free PMC article.

9

Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?

Hofman N, Wilde AA, Tan HL. Hofman N, et al. Eur Heart J. 2007 Jun;28(11):1399. doi: 10.1093/eurheartj/ehm118. Epub 2007 May 5. Eur Heart J. 2007. PMID: 17483524 No abstract available.

10

Contribution of inherited heart disease to sudden cardiac death in childhood.

Hofman N, Tan HL, Clur SA, Alders M, van Langen IM, Wilde AA. Hofman N, et al. Pediatrics. 2007 Oct;120(4):e967-73. doi: 10.1542/peds.2006-3751. Pediatrics. 2007. PMID: 17908752

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