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Page 1
Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol).
Fiot E, Alauze B, Donadille B, Samara-Boustani D, Houang M, De Filippo G, Bachelot A, Delcour C, Beyler C, Bois E, Bourrat E, Bui Quoc E, Bourcigaux N, Chaussain C, Cohen A, Cohen-Solal M, Da Costa S, Dossier C, Ederhy S, Elmaleh M, Iserin L, Lengliné H, Poujol-Robert A, Roulot D, Viala J, Albarel F, Bismuth E, Bernard V, Bouvattier C, Brac A, Bretones P, Chabbert-Buffet N, Chanson P, Coutant R, de Warren M, Demaret B, Duranteau L, Eustache F, Gautheret L, Gelwane G, Gourbesville C, Grynberg M, Gueniche K, Jorgensen C, Kerlan V, Lebrun C, Lefevre C, Lorenzini F, Manouvrier S, Pienkowski C, Reynaud R, Reznik Y, Siffroi JP, Tabet AC, Tauber M, Vautier V, Tauveron I, Wambre S, Zenaty D, Netchine I, Polak M, Touraine P, Carel JC, Christin-Maitre S, Léger J. Fiot E, et al. Among authors: bourrat e. Orphanet J Rare Dis. 2022 Jul 12;17(Suppl 1):261. doi: 10.1186/s13023-022-02423-5. Orphanet J Rare Dis. 2022. PMID: 35821070 Free PMC article.
Pain and quality of life evaluation in patients with localized epidermolysis bullosa simplex.
Brun J, Chiaverini C, Devos C, Leclerc-Mercier S, Mazereeuw J, Bourrat E, Maruani A, Mallet S, Abasq C, Phan A, Vabres P, Martin L, Bodemer C, Lagrange S, Lacour JP; Research Group of the French Society of Pediatric Dermatology. Brun J, et al. Among authors: bourrat e. Orphanet J Rare Dis. 2017 Jun 28;12(1):119. doi: 10.1186/s13023-017-0666-5. Orphanet J Rare Dis. 2017. PMID: 28659151 Free PMC article.
[PELVIS/SACRAL syndrome with livedoid haemangioma and amniotic band].
Bourrat E, Lemarchand-Venencie F, Jacquemont ML, El Ghoneimi A, Wassef M, Leger J, Morel P. Bourrat E, et al. Ann Dermatol Venereol. 2008 Dec;135(12):855-9. doi: 10.1016/j.annder.2008.05.022. Epub 2008 Nov 6. Ann Dermatol Venereol. 2008. PMID: 19084698 French.
Oral epigallocatechin-3-gallate for treatment of dystrophic epidermolysis bullosa: a multicentre, randomized, crossover, double-blind, placebo-controlled clinical trial.
Chiaverini C, Roger C, Fontas E, Bourrat E, Bourdon-Lanoy E, Labrèze C, Mazereeuw J, Vabres P, Bodemer C, Lacour JP. Chiaverini C, et al. Among authors: bourrat e. Orphanet J Rare Dis. 2016 Mar 25;11:31. doi: 10.1186/s13023-016-0411-5. Orphanet J Rare Dis. 2016. PMID: 27015660 Free PMC article. Clinical Trial.
Alitretinoin reduces erythema in inherited ichthyosis.
Onnis G, Chiaverini C, Hickman G, Dreyfus I, Fischer J, Bourrat E, Mazereeuw-Hautier J. Onnis G, et al. Among authors: bourrat e. Orphanet J Rare Dis. 2018 Apr 4;13(1):46. doi: 10.1186/s13023-018-0783-9. Orphanet J Rare Dis. 2018. PMID: 29618363 Free PMC article.
Cutaneous lipomas and macrocephaly as early signs of PTEN hamartoma tumor syndrome.
Martin H, Bessis D, Bourrat E, Mazereeuw-Hautier J, Morice-Picard F, Balguerie X, Chiaverini C; Groupe de Recherche de la Société Française de Dermatologie Pédiatrique. Martin H, et al. Among authors: bourrat e. Pediatr Dermatol. 2020 Sep;37(5):839-843. doi: 10.1111/pde.14265. Epub 2020 Jul 13. Pediatr Dermatol. 2020. PMID: 32657433
177 results