Wilde AAM - Search Results

1

In Children and Adolescents From Brugada Syndrome-Families, Only SCN5A Mutation Carriers Develop a Type-1 ECG Pattern Induced By Fever.

Peltenburg PJ, Blom NA, Vink AS, Kammeraad JAE, Breur HJMPJ, Rammeloo LAJ, Wilde AAM, Clur SB. Peltenburg PJ, et al. Among authors: wilde aam. Circulation. 2020 Jul 7;142(1):89-91. doi: 10.1161/CIRCULATIONAHA.120.045720. Epub 2020 Jul 6. Circulation. 2020. PMID: 32628552 No abstract available.

2

"Brugada" syndrome: clinical data and suggested pathophysiological mechanism.

Alings M, Wilde A. Alings M, et al. Circulation. 1999 Feb 9;99(5):666-73. doi: 10.1161/01.cir.99.5.666. Circulation. 1999. PMID: 9950665 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

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. 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.

5

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.

6

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

7

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

8

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

9

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

10

Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndrome.

Eckardt L, Probst V, Smits JP, Bahr ES, Wolpert C, Schimpf R, Wichter T, Boisseau P, Heinecke A, Breithardt G, Borggrefe M, LeMarec H, Böcker D, Wilde AA. Eckardt L, et al. Circulation. 2005 Jan 25;111(3):257-63. doi: 10.1161/01.CIR.0000153267.21278.8D. Epub 2005 Jan 10. Circulation. 2005. PMID: 15642768

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