Wilde AA - Search Results

1

A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families.

Smits JP, Koopmann TT, Wilders R, Veldkamp MW, Opthof T, Bhuiyan ZA, Mannens MM, Balser JR, Tan HL, Bezzina CR, Wilde AA. Smits JP, et al. Among authors: wilde aa. J Mol Cell Cardiol. 2005 Jun;38(6):969-81. doi: 10.1016/j.yjmcc.2005.02.024. Epub 2005 Apr 1. J Mol Cell Cardiol. 2005. PMID: 15910881

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

A dominant negative isoform of the long QT syndrome 1 gene product.

Demolombe S, Baró I, Péréon Y, Bliek J, Mohammad-Panah R, Pollard H, Morid S, Mannens M, Wilde A, Barhanin J, Charpentier F, Escande D. Demolombe S, et al. J Biol Chem. 1998 Mar 20;273(12):6837-43. doi: 10.1074/jbc.273.12.6837. J Biol Chem. 1998. PMID: 9506986 Free article.

4

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

5

Transgenic mice overexpressing human KvLQT1 dominant-negative isoform. Part I: Phenotypic characterisation.

Demolombe S, Lande G, Charpentier F, van Roon MA, van den Hoff MJ, Toumaniantz G, Baro I, Guihard G, Le Berre N, Corbier A, de Bakker J, Opthof T, Wilde A, Moorman AF, Escande D. Demolombe S, et al. Cardiovasc Res. 2001 May;50(2):314-27. doi: 10.1016/s0008-6363(01)00231-0. Cardiovasc Res. 2001. PMID: 11334835

6

A calcium sensor in the sodium channel modulates cardiac excitability.

Tan HL, Kupershmidt S, Zhang R, Stepanovic S, Roden DM, Wilde AA, Anderson ME, Balser JR. Tan HL, et al. Among authors: wilde aa. Nature. 2002 Jan 24;415(6870):442-7. doi: 10.1038/415442a. Nature. 2002. PMID: 11807557

7

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: wilde aa. Cardiovasc Res. 2002 Feb 15;53(3):770-6. doi: 10.1016/s0008-6363(01)00477-1. Cardiovasc Res. 2002. PMID: 11861047

8

Understanding torsade de pointes: a bridge to tailored drug therapy?

Tan HL, Wilde AA. Tan HL, et al. Among authors: wilde aa. Cardiovasc Drugs Ther. 2002 Mar;16(2):87-8. doi: 10.1023/a:1015781429700. Cardiovasc Drugs Ther. 2002. PMID: 12090899 No abstract available.

9

Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients.

Smits JP, Eckardt L, Probst V, Bezzina CR, Schott JJ, Remme CA, Haverkamp W, Breithardt G, Escande D, Schulze-Bahr E, LeMarec H, Wilde AA. Smits JP, et al. Among authors: wilde aa. J Am Coll Cardiol. 2002 Jul 17;40(2):350-6. doi: 10.1016/s0735-1097(02)01962-9. J Am Coll Cardiol. 2002. PMID: 12106943 Free article.

10

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

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