Wilde AAM - Search Results

1

Maturation of hiPSC-derived cardiomyocytes promotes adult alternative splicing of SCN5A and reveals changes in sodium current associated with cardiac arrhythmia.

Campostrini G, Kosmidis G, Ward-van Oostwaard D, Davis RP, Yiangou L, Ottaviani D, Veerman CC, Mei H, Orlova VV, Wilde AAM, Bezzina CR, Verkerk AO, Mummery CL, Bellin M. Campostrini G, et al. Among authors: wilde aam. Cardiovasc Res. 2023 Mar 17;119(1):167-182. doi: 10.1093/cvr/cvac059. Cardiovasc Res. 2023. PMID: 35394010 Free PMC article.

2

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.

3

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

4

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

5

Genetic control of sodium channel function.

Tan HL, Bezzina CR, Smits JP, Verkerk AO, Wilde AA. Tan HL, et al. Cardiovasc Res. 2003 Mar 15;57(4):961-73. doi: 10.1016/s0008-6363(02)00714-9. Cardiovasc Res. 2003. PMID: 12650874 Review.

6

A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics.

Groenewegen WA, Bezzina CR, van Tintelen JP, Hoorntje TM, Mannens MM, Wilde AA, Jongsma HJ, Rook MB. Groenewegen WA, et al. Cardiovasc Res. 2003 Mar 15;57(4):1072-8. doi: 10.1016/s0008-6363(02)00838-6. Cardiovasc Res. 2003. PMID: 12650885

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

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization.

Bezzina CR, Verkerk AO, Busjahn A, Jeron A, Erdmann J, Koopmann TT, Bhuiyan ZA, Wilders R, Mannens MM, Tan HL, Luft FC, Schunkert H, Wilde AA. Bezzina CR, et al. Cardiovasc Res. 2003 Jul 1;59(1):27-36. doi: 10.1016/s0008-6363(03)00342-0. Cardiovasc Res. 2003. PMID: 12829173

9

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. 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

10

The molecular genetics of arrhythmias.

Bezzina CR, Wilde AA, Roden DM. Bezzina CR, et al. Cardiovasc Res. 2005 Aug 15;67(3):343-6. doi: 10.1016/j.cardiores.2005.06.004. Cardiovasc Res. 2005. PMID: 16005449 No abstract available.

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