Zobrazeno 1 - 10
of 340
pro vyhledávání: '"C. Blanchet Bardon"'
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 26:1014-1019
Background Efficacy and tolerance should be considered in topical treatments of chronicle affections with impaired skin barrier function such as ichthyosis. Objectives To demonstrate the efficacy of Dexeryl® in reducing severity of ichthyosis. Metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e3ece1fec1f8d4bf8673ed18fcf7468
https://doi.org/10.1111/j.1468-3083.2011.04304.x
https://doi.org/10.1111/j.1468-3083.2011.04304.x
Autor:
F. Boralevi, Sébastien Barbarot, E. Bourdon-Lanoy, Emmanuelle Bourrat, C. Blanchet-Bardon, Virginie Ribet, V. Sibaud, Didier Bessis, D. Guerrero, Christine Bodemer, Juliette Mazereeuw-Hautier, J.-F. Stalder
Publikováno v:
British Journal of Dermatology. 165:1087-1094
Summary Background Management of inherited ichthyoses is symptomatic. Despite treatment, skin symptoms have a major impact on patients’ quality of life (QoL). Objectives To assess the short- and medium-term efficacy of hydrotherapy on QoL and clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a793740a03d527159ccbc743e9d9198
https://doi.org/10.1111/j.1365-2133.2011.10510.x
https://doi.org/10.1111/j.1365-2133.2011.10510.x
Peut-on traiter chirurgicalement le Mal de Meleda (kératodermie palmoplantaire diffuse de Siemens) ?
Publikováno v:
Annales de Chirurgie Plastique Esthétique. 54:152-155
Resume Introduction Le Mal de Meleda (MDM, OMIM #248300) est une keratodermie palmoplantaire congenitale rare. Des fissures profondes sont a l’origine de douleurs et de contractures dermatogeniques. Nous rapportons le cas d’un patient ayant ete o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fbb6cc263c3583b96bd0bc1edbeeaaf
https://doi.org/10.1016/j.anplas.2008.08.003
https://doi.org/10.1016/j.anplas.2008.08.003
Autor:
M.A.M. van Steensel, Peter M. Steijlen, C Blanchet-Bardon, F.P. Vanhoutte, Christel J. Verfaille
Publikováno v:
British Journal of Dermatology. 156:965-973
Summary Background Liarozole, a retinoic acid metabolism blocking agent, has been granted orphan drug status for congenital ichthyosis by the European Commission and the U.S. Food and Drug Administration. Objectives The purpose of this trial was to i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba3f9988602772f13c8efba0506b4e65
https://doi.org/10.1111/j.1365-2133.2006.07745.x
https://doi.org/10.1111/j.1365-2133.2006.07745.x
Autor:
P. Sall N’diaye, F. Pomykala, S. Makhloufi, L. Hue, M. Colomb, F. Keller, L. Sulimovic, F. Lassau, G. Reuter, R. Triller, C. Blanchet-Bardon, A.C. Crémieux, C. Fite, M. Baccard
Publikováno v:
Journal of the European Academy of Dermatology and Venereology : JEADV. 30(1)
Background The incidence of skin cancer has reached epidemic proportions in the white population and is significantly elevated in agricultural populations, who are exposed to ultraviolet radiation during their professional activities. In 2014, the Ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f87ff92267982bc4d31971166f06d695
https://pubmed.ncbi.nlm.nih.gov/26568080
https://pubmed.ncbi.nlm.nih.gov/26568080
Autor:
Saskia Ingen-Housz-Oro, P Boudou, C. Blanchet-Bardon, F. Ibrahim, JC Souberbielle, C Bergot, Louis Dubertret
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 20:947-952
Background Vitamin D is essential for bone mineralization, and its deficiency may be the cause of skeletal fractures and osteomalacia. Geographical or ethnic factors may modulate the cutaneous synthesis of vitamin D. We hypothesized that major change
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4e98bc315fbba3b71dfb83a39d23b1e
https://doi.org/10.1111/j.1468-3083.2006.01689.x
https://doi.org/10.1111/j.1468-3083.2006.01689.x
Autor:
C. Blanchet-Bardon, S. Ingen-Housz-Oro
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 132:276-283
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f572a024e04bddd12fc5dc7dd9cab2b
https://doi.org/10.1016/s0151-9638(05)79264-4
https://doi.org/10.1016/s0151-9638(05)79264-4
Autor:
L. Dubertret, N. Rioux-Leclercq, F. Martinez, David Farhi, P. Simon, C. Fumeron, G. Cam, F. Ducret, C. Blanchet-Bardon, Saskia Ingen-Housz-Oro
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 131:963-967
Resume Introduction L’epidermolyse bulleuse dystrophique recessive d’Hallopeau-Siemens (EBDR-HS) est une dermatose bulleuse hereditaire severe, due a un deficit en collagene VII. Les infections cutanees a repetition observees dans cette affection
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5946f6d3bb23ff3ec3d6a79c1d6167f3
https://doi.org/10.1016/s0151-9638(04)93806-9
https://doi.org/10.1016/s0151-9638(04)93806-9
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 18:649-653
Background In recessive dystrophic epidermolysis bullosa (RDEB), a good nutritional balance is necessary to obtain healing of the chronic wounds. However, involvement of the oral mucosa and oesophagus stenosis may be responsible for severe nutritiona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23065e6b6e81f5ce534a3f1b1f142e7f
https://doi.org/10.1111/j.1468-3083.2004.01067.x
https://doi.org/10.1111/j.1468-3083.2004.01067.x
Autor:
C. Blanchet-Bardon, S. Ingen-Housz-Oro
Publikováno v:
EMC - Dermatologie-Cosmétologie. 1:2-18
Resume Les epidermolyses bulleuses sont des genodermatoses rares, autosomiques dominantes ou recessives, impliquant les proteines de la cohesion dermoepidermique. Ainsi, selon le siege du clivage dans la membrane basale, on distingue les epidermolyse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89505df2b1198d7101e37f2188a7f782
https://doi.org/10.1016/j.emcdc.2003.12.004
https://doi.org/10.1016/j.emcdc.2003.12.004