Hoorntje TM - Search Results

1

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: hoorntje tm. 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

2

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. Among authors: hoorntje tm. Cardiovasc Res. 2003 Mar 15;57(4):1072-8. doi: 10.1016/s0008-6363(02)00838-6. Cardiovasc Res. 2003. PMID: 12650885

3

Cardiac conduction defects associate with mutations in SCN5A.

Schott JJ, Alshinawi C, Kyndt F, Probst V, Hoorntje TM, Hulsbeek M, Wilde AA, Escande D, Mannens MM, Le Marec H. Schott JJ, et al. Among authors: hoorntje tm. Nat Genet. 1999 Sep;23(1):20-1. doi: 10.1038/12618. Nat Genet. 1999. PMID: 10471492 No abstract available.

4

Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia.

Postma AV, Denjoy I, Hoorntje TM, Lupoglazoff JM, Da Costa A, Sebillon P, Mannens MM, Wilde AA, Guicheney P. Postma AV, et al. Among authors: hoorntje tm. Circ Res. 2002 Oct 18;91(8):e21-6. doi: 10.1161/01.res.0000038886.18992.6b. Circ Res. 2002. PMID: 12386154

5

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

6

Neurophysiological effects of pediatric balloon dilatation procedures.

de Vries JW, Hoorntje TM, Sreeram N. de Vries JW, et al. Among authors: hoorntje tm. Pediatr Cardiol. 2000 Sep-Oct;21(5):461-4. doi: 10.1007/s002460010110. Pediatr Cardiol. 2000. PMID: 10982708

7

Catheter ablation of incisional atrial tachycardia using a novel mapping system: LocaLisa.

Molenschot M, Ramanna H, Hoorntje T, Wittkampf F, Hauer R, Derksen R, Sreeram N. Molenschot M, et al. Pacing Clin Electrophysiol. 2001 Nov;24(11):1616-22. doi: 10.1046/j.1460-9592.2001.01616.x. Pacing Clin Electrophysiol. 2001. PMID: 11816630

8

Clinical, pathological and molecular genetic findings in a case of neonatal Marfan syndrome.

Bresters D, Nikkels PG, Meijboom EJ, Hoorntje TM, Pals G, Beemer FA. Bresters D, et al. Among authors: hoorntje tm. Acta Paediatr. 1999 Jan;88(1):98-101. doi: 10.1080/08035259950170691. Acta Paediatr. 1999. PMID: 10090557

9

[Implantable ECG recorder revealed the diagnosis in a baby with apparent life-threatening events].

Hoorntje TM, Langerak W, Blokland-Loggers HE, Sreeram N. Hoorntje TM, et al. Ned Tijdschr Geneeskd. 1999 Sep 25;143(39):1966-9. Ned Tijdschr Geneeskd. 1999. PMID: 10526617 Dutch.

10

Device therapy for malignant neonatal long QT syndrome.

Hoorntje T, Sreeram N, de Vroet R. Hoorntje T, et al. Int J Cardiol. 1999 Dec 1;71(3):289-90. doi: 10.1016/s0167-5273(99)00151-5. Int J Cardiol. 1999. PMID: 10636538 No abstract available.

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