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Page 1
Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers.
Bougeard G, Renaux-Petel M, Flaman JM, Charbonnier C, Fermey P, Belotti M, Gauthier-Villars M, Stoppa-Lyonnet D, Consolino E, Brugières L, Caron O, Benusiglio PR, Bressac-de Paillerets B, Bonadona V, Bonaïti-Pellié C, Tinat J, Baert-Desurmont S, Frebourg T. Bougeard G, et al. Among authors: renaux petel m. J Clin Oncol. 2015 Jul 20;33(21):2345-52. doi: 10.1200/JCO.2014.59.5728. Epub 2015 May 26. J Clin Oncol. 2015. PMID: 26014290
Pyogenic Sacroiliitis in a 13-Month-Old Child: A Case Report and Literature Review.
Leroux J, Bernardini I, Grynberg L, Grandguillaume C, Michelin P, Ould Slimane M, Nectoux E, Deroussen F, Gouron R, Angelliaume A, Ilharreborde B, Renaux-Petel M. Leroux J, et al. Among authors: renaux petel m. Medicine (Baltimore). 2015 Oct;94(42):e1581. doi: 10.1097/MD.0000000000001581. Medicine (Baltimore). 2015. PMID: 26496260 Free PMC article. Review.
Diffusion tensor imaging in acute pyelonephritis in children.
Lair M, Renaux-Petel M, Hassani A, Cruypeninck Y, Vasies I, Liard A, Dacher JN, Vivier PH. Lair M, et al. Among authors: renaux petel m. Pediatr Radiol. 2018 Aug;48(8):1081-1085. doi: 10.1007/s00247-018-4146-4. Epub 2018 May 22. Pediatr Radiol. 2018. PMID: 29789888
Contribution of de novo and mosaic TP53 mutations to Li-Fraumeni syndrome.
Renaux-Petel M, Charbonnier F, Théry JC, Fermey P, Lienard G, Bou J, Coutant S, Vezain M, Kasper E, Fourneaux S, Manase S, Blanluet M, Leheup B, Mansuy L, Champigneulle J, Chappé C, Longy M, Sévenet N, Paillerets BB, Guerrini-Rousseau L, Brugières L, Caron O, Sabourin JC, Tournier I, Baert-Desurmont S, Frébourg T, Bougeard G. Renaux-Petel M, et al. J Med Genet. 2018 Mar;55(3):173-180. doi: 10.1136/jmedgenet-2017-104976. Epub 2017 Oct 25. J Med Genet. 2018. PMID: 29070607
Confirmation and further delineation of the SMG9-deficiency syndrome, a rare and severe developmental disorder.
Lecoquierre F, Bonnevalle A, Chadie A, Gayet C, Dumant-Forest C, Renaux-Petel M, Leca JB, Hazelzet T, Brasseur-Daudruy M, Louillet F, Muraine M, Coutant S, Quenez O, Boland A, Deleuze JF, Frebourg T, Goldenberg A, Saugier-Veber P, Guerrot AM, Nicolas G. Lecoquierre F, et al. Among authors: renaux petel m. Am J Med Genet A. 2019 Nov;179(11):2257-2262. doi: 10.1002/ajmg.a.61317. Epub 2019 Aug 7. Am J Med Genet A. 2019. PMID: 31390136
Intradetrusor Injections of Botulinum Toxin Type A in Children With Spina Bifida: A Multicenter Study.
Hascoet J, Peyronnet B, Forin V, Baron M, Capon G, Prudhomme T, Allenet C, Tournier S, Maurin C, Cornu JN, Bouali O, Peycelon M, Arnaud A, Renaux-Petel M, Liard A, Karsenty G, Manunta A, Game X. Hascoet J, et al. Among authors: renaux petel m. Urology. 2018 Jun;116:161-167. doi: 10.1016/j.urology.2018.02.033. Epub 2018 Mar 6. Urology. 2018. PMID: 29522865
Drastic effect of germline TP53 missense mutations in Li-Fraumeni patients.
Zerdoumi Y, Aury-Landas J, Bonaïti-Pellié C, Derambure C, Sesboüé R, Renaux-Petel M, Frebourg T, Bougeard G, Flaman JM. Zerdoumi Y, et al. Among authors: renaux petel m. Hum Mutat. 2013 Mar;34(3):453-61. doi: 10.1002/humu.22254. Epub 2013 Feb 11. Hum Mutat. 2013. PMID: 23172776
11 results