Groenewegen WA - Search Results

1

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

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. Among authors: groenewegen wa. 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

Na+ channel mutation leading to loss of function and non-progressive cardiac conduction defects.

Herfst LJ, Potet F, Bezzina CR, Groenewegen WA, Le Marec H, Hoorntje TM, Demolombe S, Baró I, Escande D, Jongsma HJ, Wilde AA, Rook MB. Herfst LJ, et al. Among authors: groenewegen wa. J Mol Cell Cardiol. 2003 May;35(5):549-57. doi: 10.1016/s0022-2828(03)00078-6. J Mol Cell Cardiol. 2003. PMID: 12738236

5

Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation.

Firouzi M, Ramanna H, Kok B, Jongsma HJ, Koeleman BP, Doevendans PA, Groenewegen WA, Hauer RN. Firouzi M, et al. Among authors: groenewegen wa. Circ Res. 2004 Aug 20;95(4):e29-33. doi: 10.1161/01.RES.0000141134.64811.0a. Epub 2004 Aug 5. Circ Res. 2004. PMID: 15297374

6

Polymorphisms in human connexin40 gene promoter are associated with increased risk of hypertension in men.

Firouzi M, Kok B, Spiering W, Busjahn A, Bezzina CR, Ruijter JM, Koeleman BP, Schipper M, Groenewegen WA, Jongsma HJ, de Leeuw PW. Firouzi M, et al. Among authors: groenewegen wa. J Hypertens. 2006 Feb;24(2):325-30. doi: 10.1097/01.hjh.0000200512.40818.47. J Hypertens. 2006. PMID: 16508580

7

Cx40 polymorphism in human atrial fibrillation.

Hauer RNW, Groenewegen WA, Firouzi M, Ramanna H, Jongsma HJ. Hauer RNW, et al. Among authors: groenewegen wa. Adv Cardiol. 2006;42:284-291. doi: 10.1159/000092579. Adv Cardiol. 2006. PMID: 16646598

8

Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.

Rook MB, Bezzina Alshinawi C, Groenewegen WA, van Gelder IC, van Ginneken AC, Jongsma HJ, Mannens MM, Wilde AA. Rook MB, et al. Among authors: groenewegen wa. Cardiovasc Res. 1999 Dec;44(3):507-17. doi: 10.1016/s0008-6363(99)00350-8. Cardiovasc Res. 1999. PMID: 10690282

9

Gene polymorphisms and cardiac arrhythmias.

Firouzi M, Groenewegen WA. Firouzi M, et al. Among authors: groenewegen wa. Europace. 2003 Jul;5(3):235-42. doi: 10.1016/s1099-5129(03)00043-6. Europace. 2003. PMID: 12842634 Review. No abstract available.

10

The human Cx40 promoter polymorphism -44G-->A differentially affects transcriptional regulation by Sp1 and GATA4.

Firouzi M, Bierhuizen MF, Kok B, Teunissen BE, Jansen AT, Jongsma HJ, Groenewegen WA. Firouzi M, et al. Among authors: groenewegen wa. Biochim Biophys Acta. 2006 Oct;1759(10):491-6. doi: 10.1016/j.bbaexp.2006.09.002. Epub 2006 Sep 16. Biochim Biophys Acta. 2006. PMID: 17050003

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