Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Charles Faisant"'
Autor:
Laurence Bouillet, Isabelle Boccon-Gibod, Aurélie Du Thanh, Charles Faisant, Alban Deroux, C. Mansard
Publikováno v:
Journal of Clinical Immunology
Journal of Clinical Immunology, Springer Verlag, 2017, 37 (1), pp.80-84. ⟨10.1007/s10875-016-0345-7⟩
Journal of Clinical Immunology, Springer Verlag, 2017, 37 (1), pp.80-84. ⟨10.1007/s10875-016-0345-7⟩
International audience; Idiopathic non-histaminergic acquired angioedema (InH-AAE) is a rare disease characterized by AE resistant to antihistamines and a chronic course. We report five new cases of InH-AAE (two women and three men) with a rapid and
Autor:
Pauline Pralong, Aurélie Du-Thanh, Anne Gompel, Alban Deroux, Olivier Fain, Laurence Bouillet, Y. Ollivier, Isabelle Boccon-Gibod, Charles Faisant, Anne Pagnier, Kamel Djenouhat, David Launay
Publikováno v:
Clinical and Experimental Immunology
Clinical and Experimental Immunology, Wiley, 2016, 185 (3), pp.332-337. ⟨10.1111/cei.12820⟩
Clinical and Experimental Immunology, 2016, 185 (3), pp.332-337. ⟨10.1111/cei.12820⟩
Clinical and Experimental Immunology, Wiley, 2016, 185 (3), pp.332-337. ⟨10.1111/cei.12820⟩
Clinical and Experimental Immunology, 2016, 185 (3), pp.332-337. ⟨10.1111/cei.12820⟩
Summary Hereditary angioedema (HAE) is a rare disease associated with either a quantitative or qualitative deficiency in C1-inhibitor (C1-INH) or normal C1-INH. HAE with normal C1-INH is associated in 20% of cases with mutations in the gene for facto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::515baa5a6ddc72c7d7ce91a75a5ad6dc
https://hal.archives-ouvertes.fr/hal-01867239
https://hal.archives-ouvertes.fr/hal-01867239
Autor:
Charles Faisant, Alban Deroux, C. Mansard, Isabelle Boccon-Gibod, Pauline Pralong, C Dumestre Perard, C. Chatain, Laurence Bouillet
Publikováno v:
Clinical and Experimental Immunology
Clinical and Experimental Immunology, Wiley, 2016, 185 (1), pp.81-85. ⟨10.1111/cei.12789⟩
Clinical and Experimental Immunology, 2016, 185 (1), pp.81-85. ⟨10.1111/cei.12789⟩
Clinical and Experimental Immunology, Wiley, 2016, 185 (1), pp.81-85. ⟨10.1111/cei.12789⟩
Clinical and Experimental Immunology, 2016, 185 (1), pp.81-85. ⟨10.1111/cei.12789⟩
Summary Idiopathic histaminergic acquired angioedema (IH-AAE) is a common cause of recurrent angioedema without wheals. It is a mast cell-mediated disease thought to belong to the same clinical entity as chronic urticaria (CU). The objective of this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f34ec4f63486be963570b1a5d23660d4
https://hal.archives-ouvertes.fr/hal-02180372
https://hal.archives-ouvertes.fr/hal-02180372
Autor:
Charles Faisant, Céline Villier, Hervé Levesque, G. Armengol, Ygal Benhamou, Isabelle Boccon-Gibod, Laurence Bouillet, Judith Cottin, Nathalie Massy
Publikováno v:
Journal of clinical immunology. 36(1)
Bradykinin-mediated angioedema (AE) is a rare side effect of some medications, including angiotensin converting enzyme inhibitors (ACEi) and angiotensin receptor blockers (ARB). In France, side-effects to treatments are reported to the national pharm
Autor:
Jean-Claude Trinchet, Chantal Simon, Nathalie Barget, Nathalie Charnaux, Angela Sutton, Michel Beaugrand, Pierre Rufat, Pierre Nahon, Charles Faisant, Liliane Gattegno
Publikováno v:
European journal of gastroenterologyhepatology. 19(5)
BACKGROUND: Polymorphisms in genes encoding for the chemokines stromal cell-derived factor-1 (SDF-1)/CXCL12, monocyte chemotactic protein-1 (MCP-1)/CCL2, or for the chemokine receptors, CC chemokine receptor 5 (CCR5) or CC chemokine receptor 2 (CCR2)