Postma AV - Search Results

1

Identifying the evolutionary building blocks of the cardiac conduction system.

Jensen B, Boukens BJ, Postma AV, Gunst QD, van den Hoff MJ, Moorman AF, Wang T, Christoffels VM. Jensen B, et al. Among authors: postma av. PLoS One. 2012;7(9):e44231. doi: 10.1371/journal.pone.0044231. Epub 2012 Sep 11. PLoS One. 2012. PMID: 22984480 Free PMC article.

2

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

3

Candidate genes for the hereditary component of cardiac hypertrophy.

van den Hoff MJ, Postma AV, Michel MC. van den Hoff MJ, et al. Among authors: postma av. J Hypertens. 2006 Feb;24(2):273-7. doi: 10.1097/01.hjh.0000200520.93190.7d. J Hypertens. 2006. PMID: 16508570 No abstract available.

4

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

5

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.

6

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

7

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

8

Mutations in the sarcomere gene MYH7 in Ebstein anomaly.

Postma AV, van Engelen K, van de Meerakker J, Rahman T, Probst S, Baars MJ, Bauer U, Pickardt T, Sperling SR, Berger F, Moorman AF, Mulder BJ, Thierfelder L, Keavney B, Goodship J, Klaassen S. Postma AV, et al. Circ Cardiovasc Genet. 2011 Feb;4(1):43-50. doi: 10.1161/CIRCGENETICS.110.957985. Epub 2010 Dec 2. Circ Cardiovasc Genet. 2011. PMID: 21127202

9

A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q.

van de Meerakker JB, van Engelen K, Mathijssen IB, Lekanne dit Deprez RH, Lam J, Wilde AA, Baars MJ, Mannens MM, Mulder BJ, Moorman AF, Postma AV. van de Meerakker JB, et al. Among authors: postma av. Eur J Hum Genet. 2011 Jul;19(7):820-6. doi: 10.1038/ejhg.2011.33. Epub 2011 Mar 9. Eur J Hum Genet. 2011. PMID: 21386876 Free PMC article.

10

Developmental aspects of cardiac arrhythmogenesis.

Postma AV, Christoffels VM, Bezzina CR. Postma AV, et al. Cardiovasc Res. 2011 Jul 15;91(2):243-51. doi: 10.1093/cvr/cvr134. Epub 2011 May 12. Cardiovasc Res. 2011. PMID: 21565834 Review.

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