van Langen IM - Search Results

1

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. Among authors: van der smagt j, van langen im, van gelder ic. Circulation. 2006 Apr 4;113(13):1650-8. doi: 10.1161/CIRCULATIONAHA.105.609719. Epub 2006 Mar 27. Circulation. 2006. PMID: 16567567

2

Primary care professionals' views on population-based expanded carrier screening: an online focus group study.

van den Heuvel LM, Woudstra AJ, van der Hout S, Jans S, Wiersma T, Dondorp W, Birnie E, Lakeman P, Henneman L, Plantinga M, van Langen IM. van den Heuvel LM, et al. Among authors: van langen im. Fam Pract. 2023 Feb 1:cmad011. doi: 10.1093/fampra/cmad011. Online ahead of print. Fam Pract. 2023. PMID: 36722294

3

[Sudden death in young men due to arrhythmogenic right ventricular dysplasia].

Van Langen IM, Wilde AA, Mannens MA. Van Langen IM, et al. Ned Tijdschr Geneeskd. 1998 Mar 28;142(13):739-40. Ned Tijdschr Geneeskd. 1998. PMID: 9623151 Dutch. 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. 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.

5

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

6

[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.

7

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

8

[Truth after death; autopsies as a valued investigative tool].

van Langen IM, Wilde AA. van Langen IM, et al. Ned Tijdschr Geneeskd. 2000 Feb 26;144(9):451. Ned Tijdschr Geneeskd. 2000. PMID: 10719556 Dutch. No abstract available.

9

[Long QT-interval syndrome and investigation of heritability: psychological reactions in three generations in one family].

ten Kroode HF, van Langen IM, Hendriks KS, van Tintelen JP, Grosfeld FJ, Wilde AA. ten Kroode HF, et al. Among authors: van langen im, van tintelen jp. Ned Tijdschr Geneeskd. 2000 May 20;144(21):995-9. Ned Tijdschr Geneeskd. 2000. PMID: 10858789 Dutch.

10

[From gene to disease; ion channel proteins and the long QT syndrome].

Wilde AA, van Langen IM. Wilde AA, et al. Among authors: van langen im. Ned Tijdschr Geneeskd. 2000 Nov 11;144(46):2205-7. Ned Tijdschr Geneeskd. 2000. PMID: 11103258 Review. Dutch.

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