Muiño-Mosquera L - Search Results

1

A genotype-first approach to exploring Mendelian cardiovascular traits with clear external manifestations.

Wenger BM, Patel N, Lui M, Moscati A, Do R, Stewart DR, Tartaglia M, Muiño-Mosquera L, De Backer J, Kontorovich AR, Gelb BD. Wenger BM, et al. Genet Med. 2021 Jan;23(1):94-102. doi: 10.1038/s41436-020-00973-2. Epub 2020 Sep 29. Genet Med. 2021. PMID: 32989268 Free PMC article.

2

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.

3

Managing aortic aneurysms and dissections during pregnancy.

Muiño Mosquera L, De Backer J. Muiño Mosquera L, et al. Expert Rev Cardiovasc Ther. 2015 Jun;13(6):703-14. doi: 10.1586/14779072.2015.1042862. Epub 2015 May 17. Expert Rev Cardiovasc Ther. 2015. PMID: 26000563 Review.

4

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

5

Pregnancy in Women With SMAD3 Mutation.

van Hagen IM, van der Linde D, van de Laar IM, Muiño Mosquera L, De Backer J, Roos-Hesselink JW. van Hagen IM, et al. J Am Coll Cardiol. 2017 Mar 14;69(10):1356-1358. doi: 10.1016/j.jacc.2016.12.029. J Am Coll Cardiol. 2017. PMID: 28279300 Free article. No abstract available.

6

Efficacy of losartan as add-on therapy to prevent aortic growth and ventricular dysfunction in patients with Marfan syndrome: a randomized, double-blind clinical trial.

Muiño-Mosquera L, De Nobele S, Devos D, Campens L, De Paepe A, De Backer J. Muiño-Mosquera L, et al. Acta Cardiol. 2017 Dec;72(6):616-624. doi: 10.1080/00015385.2017.1314134. Epub 2017 Jun 28. Acta Cardiol. 2017. PMID: 28657492 Clinical Trial.

7

Sex, pregnancy and aortic disease in Marfan syndrome.

Renard M, Muiño-Mosquera L, Manalo EC, Tufa S, Carlson EJ, Keene DR, De Backer J, Sakai LY. Renard M, et al. PLoS One. 2017 Jul 14;12(7):e0181166. doi: 10.1371/journal.pone.0181166. eCollection 2017. PLoS One. 2017. PMID: 28708846 Free PMC article.

8

Arterial tortuosity syndrome: 40 new families and literature review.

Beyens A, Albuisson J, Boel A, Al-Essa M, Al-Manea W, Bonnet D, Bostan O, Boute O, Busa T, Canham N, Cil E, Coucke PJ, Cousin MA, Dasouki M, De Backer J, De Paepe A, De Schepper S, De Silva D, Devriendt K, De Wandele I, Deyle DR, Dietz H, Dupuis-Girod S, Fontenot E, Fischer-Zirnsak B, Gezdirici A, Ghoumid J, Giuliano F, Diéz NB, Haider MZ, Hardin JS, Jeunemaitre X, Klee EW, Kornak U, Landecho MF, Legrand A, Loeys B, Lyonnet S, Michael H, Moceri P, Mohammed S, Muiño-Mosquera L, Nampoothiri S, Pichler K, Prescott K, Rajeb A, Ramos-Arroyo M, Rossi M, Salih M, Seidahmed MZ, Schaefer E, Steichen-Gersdorf E, Temel S, Uysal F, Vanhomwegen M, Van Laer L, Van Maldergem L, Warner D, Willaert A, Collins TR, Taylor A, Davis EC, Zarate Y, Callewaert B. Beyens A, et al. Genet Med. 2018 Oct;20(10):1236-1245. doi: 10.1038/gim.2017.253. Epub 2018 Jan 11. Genet Med. 2018. PMID: 29323665 Free article.

9

Looking for the Missing Links: Challenges in the Search for Genotype-Phenotype Correlation in Marfan Syndrome.

De Backer J, Campens L, Muiño Mosquera L. De Backer J, et al. Circ Genom Precis Med. 2018 Jun;11(6):e002185. doi: 10.1161/CIRCGEN.118.002185. Circ Genom Precis Med. 2018. PMID: 29848616 No abstract available.

10

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. Circ Genom Precis Med. 2018 Jun;11(6):e002039. doi: 10.1161/CIRCGEN.117.002039. Circ Genom Precis Med. 2018. PMID: 29875124

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