van Langen IM - Search Results

1

Toward an effective exome-based genetic testing strategy in pediatric dilated cardiomyopathy.

Herkert JC, Abbott KM, Birnie E, Meems-Veldhuis MT, Boven LG, Benjamins M, du Marchie Sarvaas GJ, Barge-Schaapveld DQCM, van Tintelen JP, van der Zwaag PA, Vos YJ, Sinke RJ, van den Berg MP, van Langen IM, Jongbloed JDH. Herkert JC, et al. Among authors: van den berg mp, van langen im, van der zwaag pa, van tintelen jp. Genet Med. 2018 Nov;20(11):1374-1386. doi: 10.1038/gim.2018.9. Epub 2018 Mar 8. Genet Med. 2018. PMID: 29517769 Free article.

2

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. Among authors: van langen im, van tintelen jp. 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.

3

Novel KCNQ1 and HERG missense mutations in Dutch long-QT families.

Jongbloed RJ, Wilde AA, Geelen JL, Doevendans P, Schaap C, Van Langen I, van Tintelen JP, Cobben JM, Beaufort-Krol GC, Geraedts JP, Smeets HJ. Jongbloed RJ, et al. Hum Mutat. 1999;13(4):301-10. doi: 10.1002/(SICI)1098-1004(1999)13:4<301::AID-HUMU7>3.0.CO;2-V. Hum Mutat. 1999. PMID: 10220144

4

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

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

5

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. Among authors: van der hout ah, van den berg mp, van langen im. Circ Res. 1999 Dec 3-17;85(12):1206-13. doi: 10.1161/01.res.85.12.1206. Circ Res. 1999. PMID: 10590249

6

Gender differences in the long QT syndrome: effects of beta-adrenoceptor blockade.

Conrath CE, Wilde AA, Jongbloed RJ, Alders M, van Langen IM, van Tintelen JP, Doevendans PA, Opthof T. Conrath CE, et al. Among authors: van langen im, van tintelen jp. Cardiovasc Res. 2002 Feb 15;53(3):770-6. doi: 10.1016/s0008-6363(01)00477-1. Cardiovasc Res. 2002. PMID: 11861047

7

The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome.

Van Langen IM, Birnie E, Alders M, Jongbloed RJ, Le Marec H, Wilde AA. Van Langen IM, et al. J Med Genet. 2003 Feb;40(2):141-5. doi: 10.1136/jmg.40.2.141. J Med Genet. 2003. PMID: 12566525 Free PMC article. No abstract available.

8

Genetic knowledge and counselling skills of Dutch cardiologists: sufficient for the genomics era?

van Langen IM, Birnie E, Leschot NJ, Bonsel GJ, Wilde AA. van Langen IM, et al. Eur Heart J. 2003 Mar;24(6):560-6. doi: 10.1016/s0195-668x(02)00522-5. Eur Heart J. 2003. PMID: 12643889

9

High distress in parents whose children undergo predictive testing for long QT syndrome.

Hendriks KS, Grosfeld FJ, Wilde AA, van den Bout J, van Langen IM, van Tintelen JP, ten Kroode HF. Hendriks KS, et al. Among authors: van den bout j, van langen im, van tintelen jp. Community Genet. 2005;8(2):103-13. doi: 10.1159/000084778. Community Genet. 2005. PMID: 15925886

10

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. Clin Genet. 2005 Oct;68(4):360-8. doi: 10.1111/j.1399-0004.2005.00502.x. Clin Genet. 2005. PMID: 16143023

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