Zobrazeno 1 - 10
of 247
pro vyhledávání: '"Catherine Prost"'
Autor:
Loraine Combemale, Gérôme Bohelay, Ishaï-Yaacov Sitbon, Btisseme Ahouach, Marina Alexandre, Antoine Martin, Francis Pascal, Isaac Soued, Serge Doan, Florence Morin, Sabine Grootenboer-Mignot, Frédéric Caux, Catherine Prost-Squarcioni, Christelle Le Roux-Villet
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
BackgroundLichen planus pemphigoides (LPP), an association between lichen planus and bullous pemphigoid lesions, is a rare subepithelial autoimmune bullous disease. Mucous membrane involvement has been reported previously; however, it has never been
Externí odkaz:
https://doaj.org/article/5ff8dbb94b5a47dfb7ab8f37ba8b714c
Autor:
Gérôme Bohelay, Marina Alexandre, Christelle Le Roux-Villet, Ishaï Sitbon, Serge Doan, Isaac Soued, Jason Shourick, Laurie Rousset, Benoît Mellottee, Michel Heller, Nicole Lièvre, Coralie Zumelzu, Florence Morin, Sabine Grootenboer-Mignot, Eric Gabison, Frédéric Caux, Catherine Prost-Squarcioni, Philippe Musette
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Mucous membrane pemphigoid (MMP) is a heterogeneous group of rare, chronic, subepithelial autoimmune blistering diseases (AIBDs) with predominant involvement of mucous membranes that can be sight-threatening and life-threatening. Rituximab (RTX) has
Externí odkaz:
https://doaj.org/article/eb29a7279b8741d29aa27977d1d185fe
Autor:
Marina Alexandre, Gérôme Bohelay, Thomas Gille, Christelle Le Roux-Villet, Isaac Soued, Florence Morin, Frédéric Caux, Sabine Grootenboer-Mignot, Catherine Prost-Squarcioni
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
The role of IgE autoantibodies has been demonstrated in the pathogenesis of bullous pemphigoid for many years. Recently, omalizumab (OMZ), a humanized monoclonal anti-IgE antibody that depletes total serum IgE, has been used off-label in a few case s
Externí odkaz:
https://doaj.org/article/67b9d005cb1547d1a45b8dc2ceb29972
Autor:
Maike M. Holtsche, Nina van Beek, Takashi Hashimoto, Giovanni Di Zenzo, Detlef Zillikens, Catherine Prost-Squarcioni, Matthias Titeux, Alain Hovnanian, Enno Schmidt, Stephanie Goletz
Publikováno v:
Acta Dermato-Venereologica, Vol 101, Iss 3, p adv00420 (2021)
Epidermolysis bullosa acquisita is a pemphigoid disease characterized by autoantibodies against type VII collagen. This study compared the sensitivity and specificity of 6 diagnostic assays: type VII collagen non-collagenous domains enzyme-linked imm
Externí odkaz:
https://doaj.org/article/f3613b11dff74f828a07c99d552d3c78
Autor:
Hiroaki Iwata, Artem Vorobyev, Hiroshi Koga, Andreas Recke, Detlef Zillikens, Catherine Prost-Squarcioni, Norito Ishii, Takashi Hashimoto, Ralf J. Ludwig
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-9 (2018)
Abstract Background Epidermolysis bullosa acquisita (EBA) is an orphan autoimmune disease. Several clinical phenotypes have been described, but subepidermal blistering is characteristic of all variants. Limited data on clinical and immunopathological
Externí odkaz:
https://doaj.org/article/56530cff9fa14306a104297e7f55dbf2
Autor:
Clémence Briand, Greta Gourier, Florence Poizeau, Lamia Jelti, Marie Bachelerie, Gaëlle Quéreux, Géraldine Jeudy, Marie Acquitter, Saskia Ingen-Housz-Oro, Frédéric Caux, Catherine Prost, Anne-Sophie Darrigade, Diane Heron Mermin, Emmanuel Mahé, Catherine Picart Dahan, Marie-Aleth Richard, Caroline Jade Clerc, Camille Salle De Chou, Julie Plée, Claire Abasq-Thomas, Laurent Misery, Emilie Brenaut
Publikováno v:
Acta Dermato-Venereologica, Vol 100, Iss 18, p adv00320 (2020)
Pruritus is a common symptom of bullous pemphigoid (BP), but has been poorly studied. The aim of this study was to analyse the characteristics of pruritus in patients with BP and its impact on their quality of life. A multicentre prospective observat
Externí odkaz:
https://doaj.org/article/a5b49f78807942bfa744c611f998fcbc
Autor:
Ahmad Yatim, Gérôme Bohelay, Sabine Grootenboer-Mignot, Catherine Prost-Squarcioni, Marina Alexandre, Christelle Le Roux-Villet, Antoine Martin, Eve Maubec, Frédéric Caux
Publikováno v:
Frontiers in Medicine, Vol 6 (2019)
A 64-year-old patient developed a widespread autoimmune mucocutaneous blistering disease 3 weeks after the initiation of the anti-programmed death-1 (anti-PD-1) pembrolizumab therapy administered for a locally advanced cutaneous squamous cell carcino
Externí odkaz:
https://doaj.org/article/3a69fdc0aab7424ea5287af4745d05eb
Autor:
Hiroshi Koga, Catherine Prost-Squarcioni, Hiroaki Iwata, Marcel F. Jonkman, Ralf J. Ludwig, Katja Bieber
Publikováno v:
Frontiers in Medicine, Vol 5 (2019)
Epidermolysis bullosa acquisita (EBA) is an orphan autoimmune disease. Patients with EBA suffer from chronic inflammation as well as blistering and scarring of the skin and mucous membranes. Current treatment options rely on non-specific immunosuppre
Externí odkaz:
https://doaj.org/article/2e68df84bb3e4e5aa28b6a9ba37c0513
Autor:
Catherine Prost
Publikováno v:
Desenvolvimento e Meio Ambiente, Vol 48, Iss 0 (2018)
In the 1980s, the rubber tappers' movement in Acre obtained a victory in the search for a new territorial status, concluded in the legal-spatial form of extractive reserves (resex). The social struggle claimed for an agrarian reform different from th
Externí odkaz:
https://doaj.org/article/56230aa1974f488fbd7ca514c68d5b3c
Autor:
Coralie Zumelzu, Marina Alexandre, Christelle Le Roux, Patricia Weber, Alexis Guyot, Annie Levy, Françoise Aucouturier, Sabine Mignot-Grootenboer, Frédéric Caux, Eve Maubec, Catherine Prost-Squarcioni
Publikováno v:
Frontiers in Medicine, Vol 5 (2018)
An 83-year-old patient developed erosions and a blister of the gingival mucous membrane, 6 months after discontinuation of the anti-programmed death-1 (anti PD-1) pembrolizumab therapy administered for 10 months for a metastatic melanoma. A diagnosis
Externí odkaz:
https://doaj.org/article/6af666eae4fd4a6d80703bbf6a75993d