Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mathilde Bonnet des Claustres"'
Autor:
Michel De La Brassinne, Alain Hovnanian, Guy Bricteux, C. Barbieux, Mathilde Bonnet des Claustres, Martine Bagot, Emmanuelle Bourrat
Publikováno v:
Journal of the American Academy of Dermatology. 84:1476-1480
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba8d8af0d948df2fe83ee8409a345162
https://doi.org/10.1016/j.jaad.2020.07.054
https://doi.org/10.1016/j.jaad.2020.07.054
Autor:
Claire, Barbieux, Mathilde, Bonnet des Claustres, Matthias, Fahrner, Evgeniya, Petrova, Lam C, Tsoi, Olivier, Gouin, Florent, Leturcq, Pascale, Nicaise-Roland, Christine, Bole, Vivien, Béziat, Emmanuelle, Bourrat, Oliver, Schilling, Johann E, Gudjonsson, Alain, Hovnanian
Publikováno v:
The Journal of allergy and clinical immunology. 149(4)
Netherton syndrome (NS) is a rare recessive skin disorder caused by loss-of-function mutations in SPINK5 encoding the protease inhibitor LEKTI (lymphoepithelial Kazal-type-related inhibitor). NS patients experience severe skin barrier defects, displa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c6aabf5442347f0f44167283c2f1f650
https://pubmed.ncbi.nlm.nih.gov/35218769
https://pubmed.ncbi.nlm.nih.gov/35218769
Autor:
Araksya Izmiryan, Alain Hovnanian, Matthias Titeux, Mathilde Bonnet des Claustres, Hélène Ragot
Publikováno v:
Expert opinion on emerging drugs. 25(4)
Epidermolysis Bullosa (EB) form a heterogeneous group of rare, sometimes life-threatening inherited skin diseases characterized by skin and mucosal blistering after mild trauma from birth. They display a wide range of disease severity, with multiple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1320b87886e2b8021e5e7e7aab66091f
https://pubmed.ncbi.nlm.nih.gov/33094671
https://pubmed.ncbi.nlm.nih.gov/33094671
Autor:
Corinne Brunner, Barbara Meier-Schiesser, Nicole Knöpfel, Claire Barbieux, Mathilde Bonnet des Claustres, Alain Hovnanian, Davide Donghi, Agnes Schwieger-Briel, Lisa Weibel, Isabelle Luchsinger, Martin Theiler, Michael Buettcher
Publikováno v:
JAMA Dermatology
JAMA Dermatology, American Medical Association, 2020, 156 (8), pp.907-911. ⟨10.1001/jamadermatol.2020.1019⟩
JAMA Dermatology, American Medical Association, 2020, 156 (8), pp.907-911. ⟨10.1001/jamadermatol.2020.1019⟩
International audience; ImportanceNetherton syndrome (NS) is a rare, severe genetic disorder of cornification with high morbidity. Treatment for NS has been notoriously difficult. Recent studies showed an upregulated helper T cell (TH) 17/interleukin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21e29f3e79cda5984c5a1feb6ef77af5
https://www.zora.uzh.ch/id/eprint/199692/
https://www.zora.uzh.ch/id/eprint/199692/
Autor:
Mathilde Bonnet des Claustres, Alain Hovnanian, Florent Leturcq, Claire Barbieux, Olivier Gouin, Evgeniya Petrova
Publikováno v:
Journal of Investigative Dermatology
Journal of Investigative Dermatology, Nature Publishing Group, 2020, 140, pp.1184-1194. ⟨10.1016/j.jid.2019.10.026⟩
Journal of Investigative Dermatology, Nature Publishing Group, 2020, 140, pp.1184-1194. ⟨10.1016/j.jid.2019.10.026⟩
Netherton syndrome is a rare autosomal recessive skin disease caused by loss-of-function mutations in SPINK5 encoding LEKTI protein that results in unopposed activity of epidermal kallikrein-related peptidases (KLKs), mainly KLK5, KLK7, and KLK14. Al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da63b0550cd3895bde529ac36dbaf93c
https://hal.archives-ouvertes.fr/hal-03490223/document
https://hal.archives-ouvertes.fr/hal-03490223/document
Autor:
Hovnanian Alain, Evgeniya Petrova, Mathilde Bonnet des Claustres, Florent Leturcq, Claire Barbieux, Olivier Gouin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cf673f2a15ac380a8283a55d88fd3e9
https://doi.org/10.26226/morressier.5d4980cc8fb7e44098e72d3f
https://doi.org/10.26226/morressier.5d4980cc8fb7e44098e72d3f