Campens L - Search Results

1

Intrinsic cardiomyopathy in Marfan syndrome: results from in-vivo and ex-vivo studies of the Fbn1C1039G/+ model and longitudinal findings in humans.

Campens L, Renard M, Trachet B, Segers P, Muino Mosquera L, De Sutter J, Sakai L, De Paepe A, De Backer J. Campens L, et al. Pediatr Res. 2015 Sep;78(3):256-63. doi: 10.1038/pr.2015.110. Epub 2015 Jun 4. Pediatr Res. 2015. PMID: 26042521

2

Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD.

Renard M, Callewaert B, Baetens M, Campens L, MacDermot K, Fryns JP, Bonduelle M, Dietz HC, Gaspar IM, Cavaco D, Stattin EL, Schrander-Stumpel C, Coucke P, Loeys B, De Paepe A, De Backer J. Renard M, et al. Among authors: campens l. Int J Cardiol. 2013 May 10;165(2):314-21. doi: 10.1016/j.ijcard.2011.08.079. Epub 2011 Sep 19. Int J Cardiol. 2013. PMID: 21937134 Free PMC article.

3

Thoracic aortic-aneurysm and dissection in association with significant mitral valve disease caused by mutations in TGFB2.

Renard M, Callewaert B, Malfait F, Campens L, Sharif S, del Campo M, Valenzuela I, Mcwilliam C, Coucke P, De Paepe A, De Backer J. Renard M, et al. Among authors: campens l. Int J Cardiol. 2013 May 25;165(3):584-7. doi: 10.1016/j.ijcard.2012.09.029. Epub 2012 Oct 25. Int J Cardiol. 2013. PMID: 23102774 No abstract available.

4

Characterization of cardiovascular involvement in pseudoxanthoma elasticum families.

Campens L, Vanakker OM, Trachet B, Segers P, Leroy BP, De Zaeytijd J, Voet D, De Paepe A, De Backer T, De Backer J. Campens L, et al. Arterioscler Thromb Vasc Biol. 2013 Nov;33(11):2646-52. doi: 10.1161/ATVBAHA.113.301901. Epub 2013 Aug 22. Arterioscler Thromb Vasc Biol. 2013. PMID: 23968982

5

Genes in thoracic aortic aneurysms/dissections - do they matter?

De Backer J, Campens L, De Paepe A. De Backer J, et al. Among authors: campens l. Ann Cardiothorac Surg. 2013 Jan;2(1):73-82. doi: 10.3978/j.issn.2225-319X.2012.12.01. Ann Cardiothorac Surg. 2013. PMID: 23977562 Free PMC article. No abstract available.

6

New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissections.

Campens L, Renard M, Callewaert B, Coucke P, De Backer J, De Paepe A. Campens L, et al. Pol Arch Med Wewn. 2013;123(12):693-700. doi: 10.20452/pamw.2015. Epub 2013 Dec 16. Pol Arch Med Wewn. 2013. PMID: 24343123 Free article. Review.

7

Absence of cardiovascular manifestations in a haploinsufficient Tgfbr1 mouse model.

Renard M, Trachet B, Casteleyn C, Campens L, Cornillie P, Callewaert B, Deleye S, Vandeghinste B, van Heijningen PM, Dietz H, De Vos F, Essers J, Staelens S, Segers P, Loeys B, Coucke P, De Paepe A, De Backer J. Renard M, et al. Among authors: campens l. PLoS One. 2014 Feb 24;9(2):e89749. doi: 10.1371/journal.pone.0089749. eCollection 2014. PLoS One. 2014. PMID: 24587008 Free PMC article.

8

Reference values for echocardiographic assessment of the diameter of the aortic root and ascending aorta spanning all age categories.

Campens L, Demulier L, De Groote K, Vandekerckhove K, De Wolf D, Roman MJ, Devereux RB, De Paepe A, De Backer J. Campens L, et al. Am J Cardiol. 2014 Sep 15;114(6):914-20. doi: 10.1016/j.amjcard.2014.06.024. Epub 2014 Jul 3. Am J Cardiol. 2014. PMID: 25092193

9

Gene panel sequencing in heritable thoracic aortic disorders and related entities - results of comprehensive testing in a cohort of 264 patients.

Campens L, Callewaert B, Muiño Mosquera L, Renard M, Symoens S, De Paepe A, Coucke P, De Backer J. Campens L, et al. Orphanet J Rare Dis. 2015 Feb 3;10:9. doi: 10.1186/s13023-014-0221-6. Orphanet J Rare Dis. 2015. PMID: 25644172 Free PMC article.

10

Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and Dissections.

De Backer J, Renard M, Campens L, Mosquera LM, De Paepe A, Coucke P, Callewaert B, Kodolitsch Yv. De Backer J, et al. Among authors: campens l. Curr Pharm Des. 2015;21(28):4061-75. doi: 10.2174/1381612821666150826093152. Curr Pharm Des. 2015. PMID: 26306841 Review.

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