Mulder BJM - Search Results

1

Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.

Page DJ, Miossec MJ, Williams SG, Monaghan RM, Fotiou E, Cordell HJ, Sutcliffe L, Topf A, Bourgey M, Bourque G, Eveleigh R, Dunwoodie SL, Winlaw DS, Bhattacharya S, Breckpot J, Devriendt K, Gewillig M, Brook JD, Setchfield KJ, Bu'Lock FA, O'Sullivan J, Stuart G, Bezzina CR, Mulder BJM, Postma AV, Bentham JR, Baron M, Bhaskar SS, Black GC, Newman WG, Hentges KE, Lathrop GM, Santibanez-Koref M, Keavney BD. Page DJ, et al. Among authors: mulder bjm. Circ Res. 2019 Feb 15;124(4):553-563. doi: 10.1161/CIRCRESAHA.118.313250. Circ Res. 2019. PMID: 30582441 Free PMC article.

2

Preoperative thresholds for pulmonary valve replacement in patients with corrected tetralogy of Fallot using cardiovascular magnetic resonance.

Oosterhof T, van Straten A, Vliegen HW, Meijboom FJ, van Dijk AP, Spijkerboer AM, Bouma BJ, Zwinderman AH, Hazekamp MG, de Roos A, Mulder BJ. Oosterhof T, et al. Circulation. 2007 Jul 31;116(5):545-51. doi: 10.1161/CIRCULATIONAHA.106.659664. Epub 2007 Jul 9. Circulation. 2007. PMID: 17620511 Free article.

3

Survival into seventh decade after a potts palliation for tetralogy of Fallot.

Oosterhof T, Jacobs M, Cramer MJ, Mulder BJ. Oosterhof T, et al. Congenit Heart Dis. 2007 Jan-Feb;2(1):55-7. doi: 10.1111/j.1747-0803.2007.00072.x. Congenit Heart Dis. 2007. PMID: 18377517

4

Gender and outcome in adult congenital heart disease.

Verheugt CL, Uiterwaal CS, van der Velde ET, Meijboom FJ, Pieper PG, Vliegen HW, van Dijk AP, Bouma BJ, Grobbee DE, Mulder BJ. Verheugt CL, et al. Circulation. 2008 Jul 1;118(1):26-32. doi: 10.1161/CIRCULATIONAHA.107.758086. Epub 2008 Jun 16. Circulation. 2008. PMID: 18559697 Free article.

5

Prevalence of congenital heart defects in neuroblastoma patients: a cohort study and systematic review of literature.

van Engelen K, Merks JH, Lam J, Kremer LC, Backes M, Baars MJ, van der Pal HJ, Postma AV, Versteeg R, Caron HN, Mulder BJ. van Engelen K, et al. Eur J Pediatr. 2009 Sep;168(9):1081-90. doi: 10.1007/s00431-008-0891-y. Epub 2008 Dec 17. Eur J Pediatr. 2009. PMID: 19089449 Free PMC article. Review.

6

Tricuspid valve surgery in adults with a dysfunctional systemic right ventricle: repair or replace?

Scherptong RW, Vliegen HW, Winter MM, Holman ER, Mulder BJ, van der Wall EE, Hazekamp MG. Scherptong RW, et al. Circulation. 2009 Mar 24;119(11):1467-72. doi: 10.1161/CIRCULATIONAHA.108.805135. Epub 2009 Mar 9. Circulation. 2009. PMID: 19273722

7

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. Heart. 2010 Apr;96(8):621-4. doi: 10.1136/hrt.2009.182642. Heart. 2010. PMID: 20357389

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

Pregnancy in women with corrected tetralogy of Fallot: occurrence and predictors of adverse events.

Balci A, Drenthen W, Mulder BJ, Roos-Hesselink JW, Voors AA, Vliegen HW, Moons P, Sollie KM, van Dijk AP, van Veldhuisen DJ, Pieper PG. Balci A, et al. Am Heart J. 2011 Feb;161(2):307-13. doi: 10.1016/j.ahj.2010.10.027. Epub 2011 Jan 15. Am Heart J. 2011. PMID: 21315213 Free article.

10

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. 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.

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