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Isolated left ventricular non-compaction in adults: clinical and echocardiographic features in 105 patients. Results from a French registry.
Habib G, Charron P, Eicher JC, Giorgi R, Donal E, Laperche T, Boulmier D, Pascal C, Logeart D, Jondeau G, Cohen-Solal A; Working Groups 'Heart Failure and Cardiomyopathies' and 'Echocardiography' of the French Society of Cardiology. Habib G, et al. Among authors: pascal c. Eur J Heart Fail. 2011 Feb;13(2):177-85. doi: 10.1093/eurjhf/hfq225. Epub 2010 Dec 29. Eur J Heart Fail. 2011. PMID: 21193437 Free article.
[Non-compaction of the myocardium in childhood].
Pascal C, Lefèvre M; Société Française de Cardiologie. Pascal C, et al. Arch Mal Coeur Vaiss. 2005 May;98(5):443-8. Arch Mal Coeur Vaiss. 2005. PMID: 15966591 French.
11q24.2q24.3 microdeletion in two families presenting features of Jacobsen syndrome, without intellectual disability: Role of FLI1, ETS1, and SENCR long noncoding RNA.
Conrad S, Demurger F, Moradkhani K, Pichon O, Le Caignec C, Pascal C, Thomas C, Bayart S, Perlat A, Dubourg C, Jaillard S, Nizon M. Conrad S, et al. Among authors: pascal c. Am J Med Genet A. 2019 Jun;179(6):993-1000. doi: 10.1002/ajmg.a.61113. Epub 2019 Mar 19. Am J Med Genet A. 2019. PMID: 30888095 Free article. Review.
Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients With Coarctation of the Aorta.
Sanchez-Castro M, Eldjouzi H, Charpentier E, Busson PF, Hauet Q, Lindenbaum P, Delasalle-Guyomarch B, Baudry A, Pichon O, Pascal C, Lefort B, Bajolle F, Pezard P, Schott JJ, Dina C, Redon R, Gournay V, Bonnet D, Le Caignec C. Sanchez-Castro M, et al. Among authors: pascal c. Circ Cardiovasc Genet. 2016 Feb;9(1):86-94. doi: 10.1161/CIRCGENETICS.115.001213. Epub 2015 Dec 7. Circ Cardiovasc Genet. 2016. PMID: 26643481
98 results