Coucke P - Search Results

1

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: coucke p. Curr Pharm Des. 2015;21(28):4061-75. doi: 10.2174/1381612821666150826093152. Curr Pharm Des. 2015. PMID: 26306841 Review.

2

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. Among authors: coucke p. 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.

3

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. Among authors: coucke p. 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.

4

Genes in Thoracic Aortic Aneurysms and Dissections - Do they Matter?: Translation and Integration of Research and Modern Genetic Techniques into Daily Clinical Practice.

De Backer J, Renard M, Campens L, François K, Callewaert B, Coucke P, De Paepe A. De Backer J, et al. Among authors: coucke p. Aorta (Stamford). 2013 Jul 1;1(2):135-45. doi: 10.12945/j.aorta.2013.13-024. eCollection 2013 Jul. Aorta (Stamford). 2013. PMID: 26798687 Free PMC article.

5

Mutation analysis of the FBN1 gene in patients with Marfan syndrome.

Coucke P, Van Acker P, De Paepe A. Coucke P, et al. Methods Mol Med. 2006;126:81-95. doi: 10.1385/1-59745-088-X:81. Methods Mol Med. 2006. PMID: 16930007

6

The Ghent Marfan Trial--a randomized, double-blind placebo controlled trial with losartan in Marfan patients treated with β-blockers.

Möberg K, De Nobele S, Devos D, Goetghebeur E, Segers P, Trachet B, Vervaet C, Renard M, Coucke P, Loeys B, De Paepe A, De Backer J. Möberg K, et al. Among authors: coucke p. Int J Cardiol. 2012 Jun 14;157(3):354-8. doi: 10.1016/j.ijcard.2010.12.070. Epub 2011 Jan 15. Int J Cardiol. 2012. PMID: 21239069 Clinical Trial.

7

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: coucke p. 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.

8

Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology Guidelines for the Interpretation of Sequenced Variants in the FBN1 Gene for Marfan Syndrome: Proposal for a Disease- and Gene-Specific Guideline.

Muiño-Mosquera L, Steijns F, Audenaert T, Meerschaut I, De Paepe A, Steyaert W, Symoens S, Coucke P, Callewaert B, Renard M, De Backer J. Muiño-Mosquera L, et al. Among authors: coucke p. Circ Genom Precis Med. 2018 Jun;11(6):e002039. doi: 10.1161/CIRCGEN.117.002039. Circ Genom Precis Med. 2018. PMID: 29875124

9

Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys-Dietz syndromes.

Baetens M, Van Laer L, De Leeneer K, Hellemans J, De Schrijver J, Van De Voorde H, Renard M, Dietz H, Lacro RV, Menten B, Van Criekinge W, De Backer J, De Paepe A, Loeys B, Coucke PJ. Baetens M, et al. Hum Mutat. 2011 Sep;32(9):1053-62. doi: 10.1002/humu.21525. Epub 2011 Jul 20. Hum Mutat. 2011. PMID: 21542060

10

Utility of molecular analyses in the exploration of extreme intrafamilial variability in the Marfan syndrome.

De Backer J, Loeys B, Leroy B, Coucke P, Dietz H, De Paepe A. De Backer J, et al. Among authors: coucke p. Clin Genet. 2007 Sep;72(3):188-98. doi: 10.1111/j.1399-0004.2007.00845.x. Clin Genet. 2007. PMID: 17718856

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