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Page 1
The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma.
Lesueur F, de Lichy M, Barrois M, Durand G, Bombled J, Avril MF, Chompret A, Boitier F, Lenoir GM; French Familial Melanoma Study Group; Bressac-de Paillerets B, Baccard M, Bachollet B, Berthet P, Bonadona V, Bonnetblanc JM, Caron O, Chevrant-Breton J, Cuny JF, Dalle S, Delaunay M, Demange L, De Quatrebarbes J, Doré JF, Frénay M, Fricker JP, Gauthier-Villars M, Gesta P, Giraud S, Gorry P, Grange F, Green A, Huiart L, Janin N, Joly P, Kérob D, Lasset C, Leroux D, Limacher JM, Longy M, Mansard S, Marrou K, Martin-Denavit T, Mateus C, Maubec E, Olivier-Faivre L, Orlandini V, Pujol P, Sassolas B, Stoppa-Lyonnet D, Thomas L, Vabres P, Venat L, Wierzbicka E, Zattara H. Lesueur F, et al. Among authors: dalle s. Br J Cancer. 2008 Jul 22;99(2):364-70. doi: 10.1038/sj.bjc.6604470. Epub 2008 Jul 8. Br J Cancer. 2008. PMID: 18612309 Free PMC article.
[Pathology of the eyelid in elderly patients].
Thomas L, Dalle S. Thomas L, et al. Among authors: dalle s. J Fr Ophtalmol. 2006 Jun;29(6):672-86. doi: 10.1016/s0181-5512(06)76833-4. J Fr Ophtalmol. 2006. PMID: 16885900 Review. French.
New founder germline mutations of CDKN2A in melanoma-prone families and multiple primary melanoma development in a patient receiving levodopa treatment.
Kannengiesser C, Dalle S, Leccia MT, Avril MF, Bonadona V, Chompret A, Lasset C, Leroux D, Thomas L, Lesueur F, Lenoir G, Sarasin A, Bressac-de Paillerets B. Kannengiesser C, et al. Among authors: dalle s. Genes Chromosomes Cancer. 2007 Aug;46(8):751-60. doi: 10.1002/gcc.20461. Genes Chromosomes Cancer. 2007. PMID: 17492760
Neonatal follicular mucinosis.
Dalle S, Marrou K, Balme B, Thomas L. Dalle S, et al. Br J Dermatol. 2007 Sep;157(3):609-10. doi: 10.1111/j.1365-2133.2007.07956.x. Epub 2007 May 14. Br J Dermatol. 2007. PMID: 17501947 No abstract available.
501 results