Zobrazeno 1 - 10
of 104
pro vyhledávání: '"L Fertitta"'
Publikováno v:
Annales de Dermatologie et de Vénéréologie - FMC. 2:610-615
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58ac79a1af4104912bd0fc6eb5ca906e
https://doi.org/10.1016/j.fander.2022.05.005
https://doi.org/10.1016/j.fander.2022.05.005
Publikováno v:
Annales de Dermatologie et de Vénéréologie - FMC. 2:464-468
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5591251f22eb65918f2f73bb1faaaf80
https://doi.org/10.1016/j.fander.2022.02.003
https://doi.org/10.1016/j.fander.2022.02.003
Autor:
L. Fertitta, C. Bergqvist, M.L. Armand, S. Moryousef, S. Ferkal, A. Jannic, P. Ravaud, V.T. Tran, K. Ezzedine, P. Wolkenstein
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 36:1359-1366
Cutaneous neurofibromas (cNF), present in 95% of individuals with neurofibromatosis 1 (NF1), are considered as one of the greatest medical burden because of physical disfigurement. No specific score evaluates their impact on quality of life (QoL).To
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c7ec6a3f2cd745828bd6e2b4a309f9f
https://doi.org/10.1111/jdv.18140
https://doi.org/10.1111/jdv.18140
Publikováno v:
Annales de Dermatologie et de Vénéréologie - FMC. 1:370-381
Resume Les manifestations cliniques des maladies systemiques sont bien connues des dermatologues, qui sont souvent en premiere ligne du diagnostic. Chez l’enfant, ces maladies sont rares, parfois severes, avec souvent un retard au diagnostic. Des s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43c89f4c0e23cad399dc8cff44cd3b84
https://doi.org/10.1016/j.fander.2021.03.014
https://doi.org/10.1016/j.fander.2021.03.014
Akademický článek
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Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
L. Fertitta, C. Bergqvist, S. Moryousef, S. Ferkal, A. Jannic, P. Ravaud, V.T. Tran, K. Ezzedine, P. Wolkenstein
Publikováno v:
Annales de Dermatologie et de Vénéréologie - FMC. 2:A43-A44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0943d611ba4a65cb51ad9f669c44d682
https://doi.org/10.1016/j.fander.2022.09.025
https://doi.org/10.1016/j.fander.2022.09.025
Autor:
C Luca, V Zawar, D van Gysel, M Casals, Angela Hernández-Martín, Annabel Maruani, E Bonifazi, Christine Bodemer, F Mazzotta, T Hubiche, Ramon Grimalt, Isabel Colmenero, A Belloni-Fortina, L Martos-Cabrera, David Andina, I Grozdev, Suzanne G.M.A. Pasmans, A Chiriac, Antonio Torrelo, M P Novoa, M A Morren, M Munisami, Hagen Ott, Carmen Salavastru, Veronica A. Kinsler, A Nanda, M El-Hachem, Andrea Diociaiuti, J Ferrando, L Fertitta, A D Akkaya
Publikováno v:
Clinical and Experimental Dermatology
Clinical and Experimental Dermatology, Wiley, 2021, 46 (3), pp.451-461. ⟨10.1111/ced.14482⟩
Clinical and Experimental Dermatology, Wiley, 2021, 46 (3), pp.451-461. ⟨10.1111/ced.14482⟩
The current COVID-19 pandemic is caused by the SARS-CoV-2 coronavirus. The initial recognized symptoms were respiratory, sometimes culminating in severe respiratory distress requiring ventilation, and causing death in a percentage of those infected.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1abf8753dd9a43ff7c05a8ed5c5dd8b0
https://doi.org/10.1111/ced.14482
https://doi.org/10.1111/ced.14482
Autor:
Claire Hotz, D. Sawan, Pierre Wolkenstein, J.P. Méningaud, B. Hersant, Emilie Sbidian, L. Fertitta
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 34:839-845
BACKGROUND Surgery is a radical treatment for hidradenitis suppurativa (HS) and may be considered as the only one potentially curative. OBJECTIVES To characterize HS recurrence in patients after surgery and assess the risk factors of recurrence. METH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5315e7053f098feeec9118ed8c9fed4
https://doi.org/10.1111/jdv.16135
https://doi.org/10.1111/jdv.16135
Autor:
C, Bergqvist, L, Fertitta, K, Ezzedine, A, Jannic, O, Zehou, S, Ferkal, P, Combemale, S, Barbarot, J, Mazereeuw-Hautier, E, Sbidian, P, Wolkenstein, Jacques, Zeller
Publikováno v:
Journal of the European Academy of Dermatology and Venereology : JEADVReferences. 36(5)
Neurofibromatosis 1 (NF1) is one of the most common inherited disorders characterized by mutations in the tumour suppressor gene NF1. Its clinical manifestations are highly variable and unpredictable. A specific NF1 mutation does not predict the seve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c02d6469bb7ddef096138c2421b0dae6
https://pubmed.ncbi.nlm.nih.gov/35098592
https://pubmed.ncbi.nlm.nih.gov/35098592