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Page 1
ALK germline mutations in patients with neuroblastoma: a rare and weakly penetrant syndrome.
Bourdeaut F, Ferrand S, Brugières L, Hilbert M, Ribeiro A, Lacroix L, Bénard J, Combaret V, Michon J, Valteau-Couanet D, Isidor B, Rialland X, Poirée M, Defachelles AS, Peuchmaur M, Schleiermacher G, Pierron G, Gauthier-Villars M, Janoueix-Lerosey I, Delattre O; Comité Neuroblastome of the Société Francaise de Cancérologie. Bourdeaut F, et al. Among authors: ferrand s. Eur J Hum Genet. 2012 Mar;20(3):291-7. doi: 10.1038/ejhg.2011.195. Epub 2011 Nov 9. Eur J Hum Genet. 2012. PMID: 22071890 Free PMC article.
Characterization of rearrangements involving the ALK gene reveals a novel truncated form associated with tumor aggressiveness in neuroblastoma.
Cazes A, Louis-Brennetot C, Mazot P, Dingli F, Lombard B, Boeva V, Daveau R, Cappo J, Combaret V, Schleiermacher G, Jouannet S, Ferrand S, Pierron G, Barillot E, Loew D, Vigny M, Delattre O, Janoueix-Lerosey I. Cazes A, et al. Among authors: ferrand s. Cancer Res. 2013 Jan 1;73(1):195-204. doi: 10.1158/0008-5472.CAN-12-1242. Epub 2012 Nov 8. Cancer Res. 2013. PMID: 23139213
Breakpoint features of genomic rearrangements in neuroblastoma with unbalanced translocations and chromothripsis.
Boeva V, Jouannet S, Daveau R, Combaret V, Pierre-Eugène C, Cazes A, Louis-Brennetot C, Schleiermacher G, Ferrand S, Pierron G, Lermine A, Rio Frio T, Raynal V, Vassal G, Barillot E, Delattre O, Janoueix-Lerosey I. Boeva V, et al. Among authors: ferrand s. PLoS One. 2013 Aug 26;8(8):e72182. doi: 10.1371/journal.pone.0072182. eCollection 2013. PLoS One. 2013. PMID: 23991058 Free PMC article.
Clinical characteristics and outcome of patients with neuroblastoma presenting genomic amplification of loci other than MYCN.
Guimier A, Ferrand S, Pierron G, Couturier J, Janoueix-Lerosey I, Combaret V, Mosseri V, Thebaud E, Gambart M, Plantaz D, Marabelle A, Coze C, Rialland X, Fasola S, Lapouble E, Fréneaux P, Peuchmaur M, Michon J, Delattre O, Schleiermacher G. Guimier A, et al. Among authors: ferrand s. PLoS One. 2014 Jul 11;9(7):e101990. doi: 10.1371/journal.pone.0101990. eCollection 2014. PLoS One. 2014. PMID: 25013904 Free PMC article.
Homozygous PTEN deletion in neuroblastoma arising in a child with Cowden syndrome.
Bourdeaut F, Isidor B, Ferrand S, Thomas C, Moreau A, Leclair MD, David A, Pierron G, Le Caignec C, Delattre O. Bourdeaut F, et al. Among authors: ferrand s. Am J Med Genet A. 2011 Jul;155A(7):1763-6. doi: 10.1002/ajmg.a.34066. Epub 2011 Jun 10. Am J Med Genet A. 2011. PMID: 21671387 No abstract available.
[Von Recklinghausen's disease and pregnancy].
Meherzi F, Mintz P, Smadja S, Ferrand S, Ravina JH. Meherzi F, et al. Among authors: ferrand s. Rev Fr Gynecol Obstet. 1991 Oct;86(10):592-5. Rev Fr Gynecol Obstet. 1991. PMID: 1763269 Review. French.
[Quality of life analysis in patients treated for breast cancers].
Zylberberg B, Dormont D, Uzan S, Ferrand S, Antoine JM, Madelenat P, Dutranoy G, Ravina JH, Salat-Baroux J. Zylberberg B, et al. Among authors: ferrand s. J Gynecol Obstet Biol Reprod (Paris). 1994;23(8):865-73. J Gynecol Obstet Biol Reprod (Paris). 1994. PMID: 7706654 French.
33 results