Wilde AAM - Search Results

1

Determination and Interpretation of the QT Interval.

Vink AS, Neumann B, Lieve KVV, Sinner MF, Hofman N, El Kadi S, Schoenmaker MHA, Slaghekke HMJ, de Jong JSSG, Clur SB, Blom NA, Kääb S, Wilde AAM, Postema PG. Vink AS, et al. Among authors: wilde aam. Circulation. 2018 Nov 20;138(21):2345-2358. doi: 10.1161/CIRCULATIONAHA.118.033943. Circulation. 2018. PMID: 30571576

2

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

3

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

4

Proposed diagnostic criteria for the Brugada syndrome: consensus report.

Wilde AA, Antzelevitch C, Borggrefe M, Brugada J, Brugada R, Brugada P, Corrado D, Hauer RN, Kass RS, Nademanee K, Priori SG, Towbin JA; Study Group on the Molecular Basis of Arrhythmias of the European Society of Cardiology. Wilde AA, et al. Circulation. 2002 Nov 5;106(19):2514-9. doi: 10.1161/01.cir.0000034169.45752.4a. Circulation. 2002. PMID: 12417552 Review. No abstract available.

5

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill.

Groenewegen WA, Firouzi M, Bezzina CR, Vliex S, van Langen IM, Sandkuijl L, Smits JP, Hulsbeek M, Rook MB, Jongsma HJ, Wilde AA. Groenewegen WA, et al. Circ Res. 2003 Jan 10;92(1):14-22. doi: 10.1161/01.res.0000050585.07097.d7. Circ Res. 2003. PMID: 12522116

6

Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system.

Bezzina CR, Rook MB, Groenewegen WA, Herfst LJ, van der Wal AC, Lam J, Jongsma HJ, Wilde AA, Mannens MM. Bezzina CR, et al. Circ Res. 2003 Feb 7;92(2):159-68. doi: 10.1161/01.res.0000052672.97759.36. Circ Res. 2003. PMID: 12574143

7

Contribution of sodium channel mutations to bradycardia and sinus node dysfunction in LQT3 families.

Veldkamp MW, Wilders R, Baartscheer A, Zegers JG, Bezzina CR, Wilde AA. Veldkamp MW, et al. Circ Res. 2003 May 16;92(9):976-83. doi: 10.1161/01.RES.0000069689.09869.A8. Epub 2003 Apr 3. Circ Res. 2003. PMID: 12676817

8

Delay in right ventricular activation contributes to Brugada syndrome.

Tukkie R, Sogaard P, Vleugels J, de Groot IK, Wilde AA, Tan HL. Tukkie R, et al. Circulation. 2004 Mar 16;109(10):1272-7. doi: 10.1161/01.CIR.0000118467.53182.D1. Epub 2004 Mar 1. Circulation. 2004. PMID: 14993143

9

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome.

Bellocq C, van Ginneken AC, Bezzina CR, Alders M, Escande D, Mannens MM, Baró I, Wilde AA. Bellocq C, et al. Circulation. 2004 May 25;109(20):2394-7. doi: 10.1161/01.CIR.0000130409.72142.FE. Circulation. 2004. PMID: 15159330

10

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. Ann Med. 2004;36 Suppl 1:116-24. doi: 10.1080/17431380410032526. Ann Med. 2004. PMID: 15176433

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