Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Isabelle Dreyfus"'
Autor:
Isabelle Dreyfus, Aude Maza, Lauriane Rodriguez, Margot Merlos, Hélène Texier, Vanessa Rousseau, Agnès Sommet, Juliette Mazereeuw-Hautier
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background Patients with Hailey-Hailey and Darier diseases present with disabling inflammatory lesions located in large skin folds, which are often exacerbated or induced by sweating. Quality of life is highly impaired because of pain and re
Externí odkaz:
https://doaj.org/article/05374b0a600e41e7bd982e8fd8718dc8
Autor:
Giuliana Onnis, Christine Chiaverini, Geoffroy Hickman, Isabelle Dreyfus, Judith Fischer, Emmanuelle Bourrat, Juliette Mazereeuw-Hautier
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-6 (2018)
Abstract 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 eff
Externí odkaz:
https://doaj.org/article/c01097b32e26428e91a36bf99fcb4658
Autor:
Isabelle Dreyfus, Giuliana Onnis, Emilie Tournier, Olivier Dereure, Juliette Mazereeuw-Hautier
Publikováno v:
Acta Dermato-Venereologica, Vol 99, Iss 4, Pp 454-455 (2019)
Externí odkaz:
https://doaj.org/article/3cd4301df990424590a630003827e881
Autor:
Marion Godeau, Jason Shourick, Isabelle Dreyfus, Éline Casassa, Anaïs Bergeron, Maella Severino‐Freire, Céline Granier Tournier, Julie Malloizel‐Delaunay, Olivia Boccara, Hélène Aubert, Annabel Maruani, Christine Chiaverini, Christine Labrèze, Juliette Mazereeuw‐Hautier
Publikováno v:
Journal of the European Academy of Dermatology and Venereology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ffde479cbadc9bc50695d58f05157f6
https://doi.org/10.1111/jdv.19061
https://doi.org/10.1111/jdv.19061
Autor:
Juliette Mazereeuw-Hautier, Isabelle Dreyfus, Agnès Sommet, Vanessa Rousseau, Margot Merlos, Hélène Texier, Lauriane Rodriguez, Aude Maza
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Patients with Hailey-Hailey and Darier diseases present with disabling inflammatory lesions located in large skin folds, which are often exacerbated or induced by sweating. Quality of life is highly impaired because of pain and recurrent s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69d6bbe80e6a8ccd487f3c8769b5b785
https://doaj.org/article/05374b0a600e41e7bd982e8fd8718dc8
https://doaj.org/article/05374b0a600e41e7bd982e8fd8718dc8
Autor:
E. Casassa, Annabel Maruani, Hélène Aubert, Juliette Mazereeuw-Hautier, Jason Shourick, J. Malloizel-Delaunay, Sébastien Barbarot, A. Bergeron, C Labreze, A. Croiset, Isabelle Dreyfus
Publikováno v:
Journal of the European Academy of Dermatology and Venereology
Journal of the European Academy of Dermatology and Venereology, Wiley, 2021, 35 (3), pp.755-761. ⟨10.1111/jdv.17037⟩
Journal of the European Academy of Dermatology and Venereology, Wiley, 2021, 35 (3), pp.755-761. ⟨10.1111/jdv.17037⟩
International audience; Background Very few studies have evaluated the quality of life (QoL) of children suffering from low-flow vascular malformations. This is the first study investigating the influencing factors.Objectives To identify the factors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46db66a9605fb1a03c9ea19c0d187fef
https://doi.org/10.1111/jdv.17037
https://doi.org/10.1111/jdv.17037
Publikováno v:
La Presse Médicale. 48:e382-e388
Summary Background Rare diseases are defined by a prevalence of less than one out of 2000 persons. In clinical practice, their management is difficult, due to their diversity, their complexity and a lack of adapted physician training. Objective The a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89ad3023c9b0bc271b230e2de21cd700
https://doi.org/10.1016/j.lpm.2019.09.061
https://doi.org/10.1016/j.lpm.2019.09.061
Autor:
Khaled Ezzedine, Emmanuelle Bourrat, Anette Bygum, Anders Vahlquist, Christine Bodemer, A. Pietrzak, Smail Hadj-Rabia, Judith Fischer, C. Gouveia, Andrea Diociaiuti, Hagen Ott, Juliette Mazereeuw-Hautier, D.G. Paige, A. Audouze, Robert Gruber, Michael C. Rodriguez, Heiko Traupe, Matthias Schmuth, C. Amaro, D. Maier, G. Wehr, Edel A. O'Toole, M. El Hachem, M. Moreen, J.C. Sitek, Daniel Hohl, Ángela Hernández‐Martín, Agneta Gånemo, Vinzenz Oji, Nathalie Jonca, Isabelle Dreyfus, Raman Malhotra, Mateja Dolenc-Voljč, M. Aldwin, P.M. Steijlen, F. Poot
Publikováno v:
British Journal of Dermatology, 180(3), 484-495. Wiley
British Journal of Dermatology
British Journal of Dermatology, Wiley, 2019, 180 (3), pp.484-495. ⟨10.1111/bjd.16882⟩
Mazereeuw-Hautier, J, Hernandez-Martin, A, O'Toole, E A, Bygum, A, Amaro, C, Aldwin, M, Audouze, A, Bodemer, C, Bourrat, E, Diociaiuti, A, Dolenc-Voljc, M, Dreyfus, I, El Hachem, M, Fischer, J, Ganemo, A, Gouveia, C, Gruber, R, Hadj-Rabia, S, Hohl, D, Jonca, N, Ezzedine, K, Maier, D, Malhotra, R, Rodriguez, M, Ott, H, Paige, D G, Pietrzak, A, Poot, F, Schmuth, M, Sitek, J C, Steijlen, P, Wehr, G, Moreen, M, Vahlquist, A, Traupe, H & Oji, V 2019, ' Management of congenital ichthyoses : European guidelines of care: Part Two ', British Journal of Dermatology, vol. 180, no. 3, pp. 484-495 . https://doi.org/10.1111/bjd.16882
British Journal of Dermatology
British Journal of Dermatology, Wiley, 2019, 180 (3), pp.484-495. ⟨10.1111/bjd.16882⟩
Mazereeuw-Hautier, J, Hernandez-Martin, A, O'Toole, E A, Bygum, A, Amaro, C, Aldwin, M, Audouze, A, Bodemer, C, Bourrat, E, Diociaiuti, A, Dolenc-Voljc, M, Dreyfus, I, El Hachem, M, Fischer, J, Ganemo, A, Gouveia, C, Gruber, R, Hadj-Rabia, S, Hohl, D, Jonca, N, Ezzedine, K, Maier, D, Malhotra, R, Rodriguez, M, Ott, H, Paige, D G, Pietrzak, A, Poot, F, Schmuth, M, Sitek, J C, Steijlen, P, Wehr, G, Moreen, M, Vahlquist, A, Traupe, H & Oji, V 2019, ' Management of congenital ichthyoses : European guidelines of care: Part Two ', British Journal of Dermatology, vol. 180, no. 3, pp. 484-495 . https://doi.org/10.1111/bjd.16882
These guidelines for the management of congenital ichthyoses have been developed by a multidisciplinary group of European experts following a systematic review of the current literature, an expert conference held in Toulouse in 2016, and a consensus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d90b030e94f155c32b0dd13839b8759d
https://doi.org/10.1111/bjd.16882
https://doi.org/10.1111/bjd.16882
Autor:
Sylvie Cauet, Halima Yahia Cherif, M. Severino-Freire, Cristina Bulai Livideanu, Anne-Marie Tranier, Charlène Abeilhe, Isabelle Dreyfus, Fatma Jendoubi, Mathilde Negretto
Publikováno v:
Annales de Dermatologie et de Vénéréologie - FMC. 1:A286-A287
Introduction Les pathologies mastocytaires sont des maladies rares et chroniques, dont les multiples symptomes entrainent une alteration importante de la qualite de vie. PAPAM (Programme d’Accompagnement pour la Pathologie Mastocytaire) est le 1er
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc773c7aaf31e1a259f4551a90a035ba
https://doi.org/10.1016/j.fander.2021.09.302
https://doi.org/10.1016/j.fander.2021.09.302
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 145:741-748
Resume But Decrire dans une large cohorte pediatrique les caracteristiques des macules hypopigmentees ou completement depigmentees (hypo- ou achromiques) qui n’ont pas de diagnostic evident, mais pourraient faire suspecter une sclerose tubereuse de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b26d84360a74063975b9114bc600f65
https://doi.org/10.1016/j.annder.2018.07.005
https://doi.org/10.1016/j.annder.2018.07.005