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Multicentre consensus recommendations for skin care in inherited epidermolysis bullosa.
El Hachem M, Zambruno G, Bourdon-Lanoy E, Ciasulli A, Buisson C, Hadj-Rabia S, Diociaiuti A, Gouveia CF, Hernández-Martín A, de Lucas Laguna R, Dolenc-Voljč M, Tadini G, Salvatori G, De Ranieri C, Leclerc-Mercier S, Bodemer C. El Hachem M, et al. Orphanet J Rare Dis. 2014 May 20;9:76. doi: 10.1186/1750-1172-9-76. Orphanet J Rare Dis. 2014. PMID: 24884811 Free PMC article. Review.
Eosinophilic esophagitis and colonic mucosal eosinophilia in Netherton syndrome.
Paluel-Marmont C, Bellon N, Barbet P, Leclerc-Mercier S, Hadj-Rabia S, Dupont C, Bodemer C. Paluel-Marmont C, et al. J Allergy Clin Immunol. 2017 Jun;139(6):2003-2005.e1. doi: 10.1016/j.jaci.2016.10.045. Epub 2016 Dec 23. J Allergy Clin Immunol. 2017. PMID: 28025013 No abstract available.
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. 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.
Clinical variability and probable founder effect in oculocutaneous albinism type 7.
Bataille P, Michaud V, Robert MP, Bekel L, Leclerc-Mercier S, Harroche A, Célérier C, Lasseaux E, Borgel D, Bremond-Gignac D, Bodemer C, Arveiler B, Hadj-Rabia S. Bataille P, et al. Clin Genet. 2020 Mar;97(3):527-528. doi: 10.1111/cge.13655. Epub 2019 Nov 6. Clin Genet. 2020. PMID: 31694064 No abstract available.
75 results