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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 1
2003 2
2004 2
2006 1
2009 1
2010 5
2011 3
2012 2
2014 2
2015 4
2016 4
2017 4
2018 3
2019 7
2020 10
2021 7
2022 3
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50 results
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Page 1
Pathogenic FBN1 Genetic Variation and Aortic Dissection in Patients With Marfan Syndrome.
Milleron O, Arnoult F, Delorme G, Detaint D, Pellenc Q, Raffoul R, Tchitchinadze M, Langeois M, Guien C, Beroud C, Ropers J, Hanna N, Arnaud P, Gouya L, Boileau C, Jondeau G. Milleron O, et al. J Am Coll Cardiol. 2020 Mar 3;75(8):843-853. doi: 10.1016/j.jacc.2019.12.043. J Am Coll Cardiol. 2020. PMID: 32130918 Free article.
Marfan sartan saga, episode X.
Jondeau G, Milleron O, Boileau C. Jondeau G, et al. Among authors: milleron o. Eur Heart J. 2020 Nov 14;41(43):4188-4190. doi: 10.1093/eurheartj/ehaa418. Eur Heart J. 2020. PMID: 32607591 No abstract available.
[Marfan syndrome].
Jondeau G, Boileau C, Chevallier B, Delorme G, Digne F, Guiti C, Milleron O, de SaintJean M, Le Parc JM, Moura B. Jondeau G, et al. Among authors: milleron o. Arch Mal Coeur Vaiss. 2003 Nov;96(11):1081-8. Arch Mal Coeur Vaiss. 2003. PMID: 14694784 Review. French.
Marfan Syndrome: Always Evolving.
Jondeau G, Boileau C, Milleron O. Jondeau G, et al. Among authors: milleron o. Circ Cardiovasc Genet. 2017 Jun;10(3):e001785. doi: 10.1161/CIRCGENETICS.117.001785. Circ Cardiovasc Genet. 2017. PMID: 28600389 No abstract available.
Staged hybrid repair of type II thoracoabdominal aneurysms.
Pellenc Q, Roussel A, Senemaud J, Cerceau P, Iquille J, Boitet A, Leclere JB, Milleron O, Jondeau G, Castier Y. Pellenc Q, et al. Among authors: milleron o. J Vasc Surg. 2021 Jul;74(1):20-27. doi: 10.1016/j.jvs.2020.12.049. Epub 2020 Dec 16. J Vasc Surg. 2021. PMID: 33340705
Unsuspected somatic mosaicism for FBN1 gene contributes to Marfan syndrome.
Arnaud P, Morel H, Milleron O, Gouya L, Francannet C, Da Costa A, Le Goff C, Jondeau G, Boileau C, Hanna N. Arnaud P, et al. Among authors: milleron o. Genet Med. 2021 May;23(5):865-871. doi: 10.1038/s41436-020-01078-6. Epub 2021 Jan 25. Genet Med. 2021. PMID: 33495528 Free PMC article.
Quantifying the Genetic Basis of Marfan Syndrome Clinical Variability.
Grange T, Aubart M, Langeois M, Benarroch L, Arnaud P, Milleron O, Eliahou L, Gross MS, Hanna N, Boileau C, Gouya L, Jondeau G. Grange T, et al. Among authors: milleron o. Genes (Basel). 2020 May 20;11(5):574. doi: 10.3390/genes11050574. Genes (Basel). 2020. PMID: 32443863 Free PMC article.
Optimising Aortic Endovascular Repair in Patients with Marfan Syndrome.
Pellenc Q, Girault A, Roussel A, De Blic R, Cerceau P, Raffoul R, Milleron O, Jondeau G, Castier Y. Pellenc Q, et al. Among authors: milleron o. Eur J Vasc Endovasc Surg. 2020 Apr;59(4):577-585. doi: 10.1016/j.ejvs.2019.09.501. Epub 2019 Dec 18. Eur J Vasc Endovasc Surg. 2020. PMID: 31865029 Free article.
Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm.
Elbitar S, Renard M, Arnaud P, Hanna N, Jacob MP, Guo DC, Tsutsui K, Gross MS, Kessler K, Tosolini L, Dattilo V, Dupont S, Jonquet J, Langeois M, Benarroch L, Aubart M, Ghaleb Y, Abou Khalil Y, Varret M, El Khoury P, Ho-Tin-Noé B, Alembik Y, Gaertner S, Isidor B, Gouya L, Milleron O, Sekiguchi K, Milewicz D, De Backer J, Le Goff C, Michel JB, Jondeau G, Sakai LY, Boileau C, Abifadel M. Elbitar S, et al. Among authors: milleron o. Genet Med. 2021 Jan;23(1):111-122. doi: 10.1038/s41436-020-00947-4. Epub 2020 Aug 28. Genet Med. 2021. PMID: 32855533 Free PMC article.
[Marfan syndrome and related disorders].
Eliahou L, Milleron O, Jondeau G. Eliahou L, et al. Among authors: milleron o. Rev Prat. 2020 Nov;70(9):1005-1009. Rev Prat. 2020. PMID: 33739763 French.
50 results