Mannens MMAM - Search Results

1

Transthyretin amyloidosis: a phenocopy of hypertrophic cardiomyopathy.

Vermeer AMC, Janssen A, Boorsma PC, Mannens MMAM, Wilde AAM, Christiaans I. Vermeer AMC, et al. Among authors: mannens mmam. Amyloid. 2017 Jun;24(2):87-91. doi: 10.1080/13506129.2017.1322573. Epub 2017 May 5. Amyloid. 2017. PMID: 28475415

2

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

3

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

4

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

5

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

6

Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome.

Verkerk AO, Wilders R, Schulze-Bahr E, Beekman L, Bhuiyan ZA, Bertrand J, Eckardt L, Lin D, Borggrefe M, Breithardt G, Mannens MM, Tan HL, Wilde AA, Bezzina CR. Verkerk AO, et al. Cardiovasc Res. 2005 Dec 1;68(3):441-53. doi: 10.1016/j.cardiores.2005.06.027. Epub 2005 Jul 25. Cardiovasc Res. 2005. PMID: 16043162

7

Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies.

Koopmann TT, Alders M, Jongbloed RJ, Guerrero S, Mannens MM, Wilde AA, Bezzina CR. Koopmann TT, et al. Heart Rhythm. 2006 Jan;3(1):52-5. doi: 10.1016/j.hrthm.2005.10.014. Heart Rhythm. 2006. PMID: 16399053

8

Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy.

van Tintelen JP, Entius MM, Bhuiyan ZA, Jongbloed R, Wiesfeld AC, Wilde AA, van der Smagt J, Boven LG, Mannens MM, van Langen IM, Hofstra RM, Otterspoor LC, Doevendans PA, Rodriguez LM, van Gelder IC, Hauer RN. van Tintelen JP, et al. Circulation. 2006 Apr 4;113(13):1650-8. doi: 10.1161/CIRCULATIONAHA.105.609719. Epub 2006 Mar 27. Circulation. 2006. PMID: 16567567

9

Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a family.

Kannankeril PJ, Bhuiyan ZA, Darbar D, Mannens MM, Wilde AA, Roden DM. Kannankeril PJ, et al. Heart Rhythm. 2006 Aug;3(8):939-44. doi: 10.1016/j.hrthm.2006.04.028. Epub 2006 May 3. Heart Rhythm. 2006. PMID: 16876743

10

Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?

Hofman N, Wilde AA, Kääb S, van Langen IM, Tanck MW, Mannens MM, Hinterseer M, Beckmann BM, Tan HL. Hofman N, et al. Eur Heart J. 2007 Mar;28(5):575-80. doi: 10.1093/eurheartj/ehl355. Epub 2006 Nov 7. Eur Heart J. 2007. PMID: 17090615

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