Postma AV - Search Results

1

Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3.

Postma AV, Bezzina CR, de Vries JF, Wilde AA, Moorman AF, Mannens MM. Postma AV, et al. Hum Genet. 2000 Jun;106(6):614-9. doi: 10.1007/s004390000308. Hum Genet. 2000. PMID: 10942109

2

A single Na(+) channel mutation causing both long-QT and Brugada syndromes.

Bezzina C, Veldkamp MW, van Den Berg MP, Postma AV, Rook MB, Viersma JW, van Langen IM, Tan-Sindhunata G, Bink-Boelkens MT, van Der Hout AH, Mannens MM, Wilde AA. Bezzina C, et al. Among authors: postma av. Circ Res. 1999 Dec 3-17;85(12):1206-13. doi: 10.1161/01.res.85.12.1206. Circ Res. 1999. PMID: 10590249

3

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. Circ Res. 2002 Oct 18;91(8):e21-6. doi: 10.1161/01.res.0000038886.18992.6b. Circ Res. 2002. PMID: 12386154

4

Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients.

Postma AV, Denjoy I, Kamblock J, Alders M, Lupoglazoff JM, Vaksmann G, Dubosq-Bidot L, Sebillon P, Mannens MM, Guicheney P, Wilde AA. Postma AV, et al. J Med Genet. 2005 Nov;42(11):863-70. doi: 10.1136/jmg.2004.028993. J Med Genet. 2005. PMID: 16272262 Free PMC article.

5

A novel early onset lethal form of catecholaminergic polymorphic ventricular tachycardia maps to chromosome 7p14-p22.

Bhuiyan ZA, Hamdan MA, Shamsi ET, Postma AV, Mannens MM, Wilde AA, Al-Gazali L. Bhuiyan ZA, et al. Among authors: postma av. J Cardiovasc Electrophysiol. 2007 Sep;18(10):1060-6. doi: 10.1111/j.1540-8167.2007.00913.x. Epub 2007 Jul 30. J Cardiovasc Electrophysiol. 2007. PMID: 17666061

6

Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features.

Bhuiyan ZA, van den Berg MP, van Tintelen JP, Bink-Boelkens MT, Wiesfeld AC, Alders M, Postma AV, van Langen I, Mannens MM, Wilde AA. Bhuiyan ZA, et al. Among authors: postma av. Circulation. 2007 Oct 2;116(14):1569-76. doi: 10.1161/CIRCULATIONAHA.107.711606. Epub 2007 Sep 17. Circulation. 2007. PMID: 17875969

7

A gain-of-function TBX5 mutation is associated with atypical Holt-Oram syndrome and paroxysmal atrial fibrillation.

Postma AV, van de Meerakker JB, Mathijssen IB, Barnett P, Christoffels VM, Ilgun A, Lam J, Wilde AA, Lekanne Deprez RH, Moorman AF. Postma AV, et al. Circ Res. 2008 Jun 6;102(11):1433-42. doi: 10.1161/CIRCRESAHA.107.168294. Epub 2008 May 1. Circ Res. 2008. PMID: 18451335

8

Developmental and genetic aspects of atrial fibrillation.

Postma AV, Dekker LR, Soufan AT, Moorman AF. Postma AV, et al. Trends Cardiovasc Med. 2009 May;19(4):123-30. doi: 10.1016/j.tcm.2009.07.003. Trends Cardiovasc Med. 2009. PMID: 19818948 Review.

9

22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia.

van Engelen K, Topf A, Keavney BD, Goodship JA, van der Velde ET, Baars MJ, Snijder S, Moorman AF, Postma AV, Mulder BJ. van Engelen K, et al. Among authors: postma av. Heart. 2010 Apr;96(8):621-4. doi: 10.1136/hrt.2009.182642. Heart. 2010. PMID: 20357389

10

Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome.

Boogerd CJ, Dooijes D, Ilgun A, Mathijssen IB, Hordijk R, van de Laar IM, Rump P, Veenstra-Knol HE, Moorman AF, Barnett P, Postma AV. Boogerd CJ, et al. Among authors: postma av. Cardiovasc Res. 2010 Oct 1;88(1):130-9. doi: 10.1093/cvr/cvq178. Epub 2010 Jun 2. Cardiovasc Res. 2010. PMID: 20519243

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