Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Emmanuelle Bourrat"'
Publikováno v:
Journal of Clinical Immunology
Autor:
Cédric Lenormand, Emmanuelle Bourrat, Matthieu Say, Christine Chiaverini, Franck Boralevi, Emmanuel Mahé, Nathalie Beneton, Marion Lagaude, Vincent Descamps, Anne-Claire Bursztejn, Eric Estève, Aurélie Acher, Christine Bodemer, Jean-Philippe Lacour, Denis Jullien, Marie-Aleth Richard, A. Phan
Publikováno v:
American Journal of Clinical Dermatology. 19:609-615
Psoriasis affects 2–4% of the population, with the most common clinical type being plaque psoriasis. The linear form of psoriasis is very rare. The literature on linear psoriasis (LP) consists of only case reports, and data are few. This study aime
Autor:
G. Onnis, Judith Fischer, Juliette Mazereeuw-Hautier, Christine Chiaverini, Emmanuelle Bourrat, Isabelle Dreyfus, Geoffroy Hickman
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-6 (2018)
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-6 (2018)
Background Acitretin is the main retinoid used to treat severe inherited ichthyosis. Alternatives may be considered if it results ineffective or there are side-effects, or for women of childbearing age. Our objective is evaluation of the effects and
Autor:
Jennifer Brun, Christine Chiaverini, Caroline Devos, Stéphanie Leclerc-Mercier, Juliette Mazereeuw, Emmanuelle Bourrat, Annabel Maruani, Stéphanie Mallet, Claire Abasq, Alice Phan, Pierre Vabres, Ludovic Martin, Christine Bodemer, Sylvie Lagrange, Jean-Philippe Lacour, the Research Group of the French Society of Pediatric Dermatology
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2017, 12 (1), pp.119. ⟨10.1186/s13023-017-0666-5⟩
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-8 (2017)
Orphanet Journal of Rare Diseases, 2017, 12 (1), pp.119. ⟨10.1186/s13023-017-0666-5⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2017, 12 (1), pp.119. ⟨10.1186/s13023-017-0666-5⟩
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-8 (2017)
Orphanet Journal of Rare Diseases, 2017, 12 (1), pp.119. ⟨10.1186/s13023-017-0666-5⟩
International audience; BackgroundA localized form of epidermolysis bullosa simplex (EBS-l) is considered one of the mildest forms of epidermolysis bullosa (EB), with blisters limited to the palms and soles. However, these lesions can be very painful
Autor:
Emmanuelle Bourrat, Christine Chiaverini, E. Bourdon-Lanoy, Coralie Roger, Christine Bodemer, Jean-Philippe Lacour, C. Labreze, E. Fontas, J. Mazereeuw, Pierre Vabres
Publikováno v:
Orphanet Journal of Rare Diseases
Recessive dystrophic epidermolysis bullosa (RDEB) is a rare genodermatosis with severe blistering. No curative treatment is available. Scientific data indicated that epigallocatechin-3-gallate (EGCG), a green tea extract, might improve the phenotype