Wilde AA - Search Results

1

Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients.

Postma AV, Denjoy I, Kamblock J, Alders M, Lupoglazoff JM, Vaksmann G, Dubosq-Bidot L, Sebillon P, Mannens MM, Guicheney P, Wilde AA. Postma AV, et al. Among authors: wilde aa. J Med Genet. 2005 Nov;42(11):863-70. doi: 10.1136/jmg.2004.028993. J Med Genet. 2005. PMID: 16272262 Free PMC article.

2

KVLQT1, the rhythm of imprinting.

Mannens M, Wilde A. Mannens M, et al. Nat Genet. 1997 Feb;15(2):113-5. doi: 10.1038/ng0297-113. Nat Genet. 1997. PMID: 9020829 No abstract available.

3

Homozygous premature truncation of the HERG protein : the human HERG knockout.

Hoorntje T, Alders M, van Tintelen P, van der Lip K, Sreeram N, van der Wal A, Mannens M, Wilde A. Hoorntje T, et al. Circulation. 1999 Sep 21;100(12):1264-7. doi: 10.1161/01.cir.100.12.1264. Circulation. 1999. PMID: 10491368

4

Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia.

Postma AV, Denjoy I, Hoorntje TM, Lupoglazoff JM, Da Costa A, Sebillon P, Mannens MM, Wilde AA, Guicheney P. Postma AV, et al. Among authors: wilde aa. Circ Res. 2002 Oct 18;91(8):e21-6. doi: 10.1161/01.res.0000038886.18992.6b. Circ Res. 2002. PMID: 12386154

5

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. Among authors: wilde aa. 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.

6

[Sudden death at young age and the importance of molecular-pathologic investigation].

Wilde AA, van Langen IM, Mannens MM, Waalewijn RA, Maes A. Wilde AA, et al. Ned Tijdschr Geneeskd. 2005 Jul 16;149(29):1601-4. Ned Tijdschr Geneeskd. 2005. PMID: 16078763 Dutch.

7

A novel early onset lethal form of catecholaminergic polymorphic ventricular tachycardia maps to chromosome 7p14-p22.

Bhuiyan ZA, Hamdan MA, Shamsi ET, Postma AV, Mannens MM, Wilde AA, Al-Gazali L. Bhuiyan ZA, et al. Among authors: wilde aa. J Cardiovasc Electrophysiol. 2007 Sep;18(10):1060-6. doi: 10.1111/j.1540-8167.2007.00913.x. Epub 2007 Jul 30. J Cardiovasc Electrophysiol. 2007. PMID: 17666061

8

Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features.

Bhuiyan ZA, van den Berg MP, van Tintelen JP, Bink-Boelkens MT, Wiesfeld AC, Alders M, Postma AV, van Langen I, Mannens MM, Wilde AA. Bhuiyan ZA, et al. Among authors: wilde aa. Circulation. 2007 Oct 2;116(14):1569-76. doi: 10.1161/CIRCULATIONAHA.107.711606. Epub 2007 Sep 17. Circulation. 2007. PMID: 17875969

9

Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation.

Alders M, Koopmann TT, Christiaans I, Postema PG, Beekman L, Tanck MW, Zeppenfeld K, Loh P, Koch KT, Demolombe S, Mannens MM, Bezzina CR, Wilde AA. Alders M, et al. Among authors: wilde aa. Am J Hum Genet. 2009 Apr;84(4):468-76. doi: 10.1016/j.ajhg.2009.02.009. Epub 2009 Mar 12. Am J Hum Genet. 2009. PMID: 19285295 Free PMC article.

10

SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome.

Probst V, Wilde AA, Barc J, Sacher F, Babuty D, Mabo P, Mansourati J, Le Scouarnec S, Kyndt F, Le Caignec C, Guicheney P, Gouas L, Albuisson J, Meregalli PG, Le Marec H, Tan HL, Schott JJ. Probst V, et al. Among authors: wilde aa. Circ Cardiovasc Genet. 2009 Dec;2(6):552-7. doi: 10.1161/CIRCGENETICS.109.853374. Epub 2009 Sep 29. Circ Cardiovasc Genet. 2009. PMID: 20031634

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