Lévy N - Search Results

1

Outcomes of 4 years of molecular genetic diagnosis on a panel of genes involved in premature aging syndromes, including laminopathies and related disorders.

Grelet M, Blanck V, Sigaudy S, Philip N, Giuliano F, Khachnaoui K, Morel G, Grotto S, Sophie J, Poirsier C, Lespinasse J, Alric L, Calvas P, Chalhoub G, Layet V, Molin A, Colson C, Marsili L, Edery P, Lévy N, De Sandre-Giovannoli A. Grelet M, et al. Among authors: levy n. Orphanet J Rare Dis. 2019 Dec 11;14(1):288. doi: 10.1186/s13023-019-1189-z. Orphanet J Rare Dis. 2019. PMID: 31829210 Free PMC article.

2

Altered splicing in prelamin A-associated premature aging phenotypes.

De Sandre-Giovannoli A, Lévy N. De Sandre-Giovannoli A, et al. Among authors: levy n. Prog Mol Subcell Biol. 2006;44:199-232. doi: 10.1007/978-3-540-34449-0_9. Prog Mol Subcell Biol. 2006. PMID: 17076270 Review.

3

MicroRNAs in hereditary and sporadic premature aging syndromes and other laminopathies.

Frankel D, Delecourt V, Harhouri K, De Sandre-Giovannoli A, Lévy N, Kaspi E, Roll P. Frankel D, et al. Among authors: levy n. Aging Cell. 2018 Aug;17(4):e12766. doi: 10.1111/acel.12766. Epub 2018 Apr 25. Aging Cell. 2018. PMID: 29696758 Free PMC article. Review.

4

Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective.

Cau P, Navarro C, Harhouri K, Roll P, Sigaudy S, Kaspi E, Perrin S, De Sandre-Giovannoli A, Lévy N. Cau P, et al. Among authors: levy n. Semin Cell Dev Biol. 2014 May;29:125-47. doi: 10.1016/j.semcdb.2014.03.021. Epub 2014 Mar 22. Semin Cell Dev Biol. 2014. PMID: 24662892 Review.

5

Pereira S, Bourgeois P, Navarro C, Esteves-Vieira V, Cau P, De Sandre-Giovannoli A, Lévy N. Pereira S, et al. Among authors: levy n. Mech Ageing Dev. 2008 Jul-Aug;129(7-8):449-59. doi: 10.1016/j.mad.2008.04.003. Epub 2008 Apr 12. Mech Ageing Dev. 2008. PMID: 18513784 Review.

6

Mesenchymal stem cells derived from patients with premature aging syndromes display hallmarks of physiological aging.

Trani JP, Chevalier R, Caron L, El Yazidi C, Broucqsault N, Toury L, Thomas M, Annab K, Binetruy B, De Sandre-Giovannoli A, Levy N, Magdinier F, Robin JD. Trani JP, et al. Among authors: levy n. Life Sci Alliance. 2022 Sep 14;5(12):e202201501. doi: 10.26508/lsa.202201501. Life Sci Alliance. 2022. PMID: 36104080 Free PMC article.

7

WITHDRAWN: Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective.

Cau P, Navarro C, Harhouri K, Roll P, Sigaudy S, Kaspi E, Perrin S, De Sandre-Giovannoli A, Lévy N. Cau P, et al. Among authors: levy n. Semin Cell Dev Biol. 2014 Mar 28:S1084-9521(14)00058-5. doi: 10.1016/j.semcdb.2014.03.022. Online ahead of print. Semin Cell Dev Biol. 2014. PMID: 24685615

8

A novel overlapping phenotype characterized by lipodystrophy, mandibular dysplasia, and dilated cardiomyopathy associated with a new mutation in the LMNA gene.

Ambrosi P, Kreitmann B, Lepidi H, Habib G, Levy N, Philip N, De Sandre-Giovannoli A. Ambrosi P, et al. Among authors: levy n. Int J Cardiol. 2016 Apr 15;209:317-8. doi: 10.1016/j.ijcard.2016.02.113. Epub 2016 Feb 16. Int J Cardiol. 2016. PMID: 26922292 No abstract available.

9

Retrospective analysis and reclassification of DYSF variants in a large French series of dysferlinopathy patients.

Charnay T, Blanck V, Cerino M, Bartoli M, Riccardi F, Bonello-Palot N, Pécheux C, Nguyen K, Lévy N, Gorokhova S, Krahn M. Charnay T, et al. Among authors: levy n. Genet Med. 2021 Aug;23(8):1574-1577. doi: 10.1038/s41436-021-01164-3. Epub 2021 Apr 29. Genet Med. 2021. PMID: 33927379 Free article.

10

Novel Exon-Skipping Therapeutic Approach for the DMD Gene Based on Asymptomatic Deletions of Exon 49.

Abaji M, Gorokhova S, Da Silva N, Busa T, Grelet M, Missirian C, Sigaudy S, Philip N, Leturcq F, Lévy N, Krahn M, Bartoli M. Abaji M, et al. Among authors: levy n. Genes (Basel). 2022 Jul 19;13(7):1277. doi: 10.3390/genes13071277. Genes (Basel). 2022. PMID: 35886062 Free PMC article.

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