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

Year Number of Results
2002 3
2003 1
2004 2
2005 1
2006 4
2007 1
2008 4
2010 2
2011 2
2012 3
2013 2
2014 3
2017 5
2019 1
2022 1
2024 0

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33 results

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Page 1
Molecular bases of progeroid syndromes.
Navarro CL, Cau P, Lévy N. Navarro CL, et al. Among authors: cau p. Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R151-61. doi: 10.1093/hmg/ddl214. Hum Mol Genet. 2006. PMID: 16987878 Review.
Lamin a truncation in Hutchinson-Gilford progeria.
De Sandre-Giovannoli A, Bernard R, Cau P, Navarro C, Amiel J, Boccaccio I, Lyonnet S, Stewart CL, Munnich A, Le Merrer M, Lévy N. De Sandre-Giovannoli A, et al. Among authors: cau p. Science. 2003 Jun 27;300(5628):2055. doi: 10.1126/science.1084125. Epub 2003 Apr 17. Science. 2003. PMID: 12702809 No abstract available.
Identification of CD146 as a novel molecular actor involved in systemic sclerosis.
Kaspi E, Heim X, Granel B, Guillet B, Stalin J, Nollet M, Bertaud-Foucault A, Robaglia-Schlupp A, Roll P, Cau P, Leroyer A, Bachelier R, Benyamine A, Dignat-George F, Blot-Chabaud M, Bardin N. Kaspi E, et al. Among authors: cau p. J Allergy Clin Immunol. 2017 Nov;140(5):1448-1451.e6. doi: 10.1016/j.jaci.2017.04.046. Epub 2017 Jun 9. J Allergy Clin Immunol. 2017. PMID: 28606586 No abstract available.
High prevalence of laminopathies among patients with metabolic syndrome.
Dutour A, Roll P, Gaborit B, Courrier S, Alessi MC, Tregouet DA, Angelis F, Robaglia-Schlupp A, Lesavre N, Cau P, Lévy N, Badens C, Morange PE. Dutour A, et al. Among authors: cau p. Hum Mol Genet. 2011 Oct 1;20(19):3779-86. doi: 10.1093/hmg/ddr294. Epub 2011 Jun 30. Hum Mol Genet. 2011. PMID: 21724554
33 results