Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Gwenola Maigne"'
Autor:
Guillaume Manson, Alexandre Thibault Jacques Maria, Florence Poizeau, François-Xavier Danlos, Marie Kostine, Solenn Brosseau, Sandrine Aspeslagh, Pauline Du Rusquec, Maxime Roger, Maud Pallix-Guyot, Marc Ruivard, Léa Dousset, Laurianne Grignou, Dimitri Psimaras, Johan Pluvy, Gilles Quéré, Franck Grados, Fanny Duval, Frederic Bourdain, Gwenola Maigne, Julie Perrin, Benoit Godbert, Beatris Irina Taifas, Alexandra Forestier, Anne-Laure Voisin, Patricia Martin-Romano, Capucine Baldini, Aurélien Marabelle, Christophe Massard, Jérôme Honnorat, Olivier Lambotte, Jean-Marie Michot
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 7, Iss 1, Pp 1-12 (2019)
Abstract Background Paraneoplastic syndromes (PNS) are autoimmune disorders specifically associated with cancer. There are few data on anti-PD-1 or anti-PD-L1 immunotherapy in patients with a PNS. Our objective was to describe the outcome for patient
Externí odkaz:
https://doaj.org/article/ca72d3ba97984c078f0aec5f8467a55e
Autor:
Benjamin Savoye, Gwenola Maigne, Evangeline Pillebout, Gaetane Planchard, Maxime Faisant, Achille Aouba, Alexandra Audemard
Publikováno v:
European Journal of Case Reports in Internal Medicine (2019)
Introduction: Immunoglobulin A vasculitis (IgAV) is a small-vessel vasculitis with IgA-dominant immune deposits. IgAV frequently involves the skin, gastrointestinal tract, joints and kidneys. In contrast to other types of small-vessel vasculitis, IgA
Externí odkaz:
https://doaj.org/article/d1c81d02c0c3452085a8f190b694e7b4
Autor:
Hubert de Boysson, Gwenola Maigne, Virginie Rieu, Alain Manrique, Samuel Deshayes, Achille Aouba, Nicolas Martin Silva, Jacques Monteil, K.H. Ly
Publikováno v:
Rheumatology. 61:400-406
Objectives The treatment of GCA relies on corticosteroids but is burdened by a high rate of relapses and adverse effects. Anti-IL-6 treatments show a clear benefit with a significant steroid-sparing effect, but late relapses occur after treatment dis
Autor:
Achille Aouba, Julien Rossignol, Matthieu Mahévas, Damien Roos-Weil, Pierre Hirsch, Anna Sevoyan, Yervand Hakobyan, Sébastien Miranda, Louis Terriou, Julie Graveleau, Gwenola Maigne, Matthieu Groh, Thomas Quemeneur, Florent Malard, Marie Sebert, Sophie Georgin-Lavialle, Artem Oganesyan, Arsène Mekinian, Nabil Belfeki, Pierre Fenaux, Matthieu Decamp, Laurent Sailler, Louis Drevon, M. Delplanque, Jerome Razanamahery
Publikováno v:
Journal of Clinical Medicine
Journal of Clinical Medicine, 2021, 10 (23), pp.5586. ⟨10.3390/jcm10235586⟩
Journal of Clinical Medicine, MDPI, 2021, 10 (23), pp.5586. ⟨10.3390/jcm10235586⟩
Journal of Clinical Medicine; Volume 10; Issue 23; Pages: 5586
Journal of Clinical Medicine, Vol 10, Iss 5586, p 5586 (2021)
Journal of Clinical Medicine, 2021, 10 (23), pp.5586. ⟨10.3390/jcm10235586⟩
Journal of Clinical Medicine, MDPI, 2021, 10 (23), pp.5586. ⟨10.3390/jcm10235586⟩
Journal of Clinical Medicine; Volume 10; Issue 23; Pages: 5586
Journal of Clinical Medicine, Vol 10, Iss 5586, p 5586 (2021)
International audience; Background: Patients with solid cancers and hematopoietic malignancy can experience systemic symptoms compatible with adult-onset Still’s disease (AOSD). The newly described VEXAS, associated with somatic UBA1 mutations, exh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00e2e510246a9ef755fc33b3b1a67b40
https://hal.sorbonne-universite.fr/hal-03511806/document
https://hal.sorbonne-universite.fr/hal-03511806/document
Autor:
Julia Moeglin, Morgane Mourguet, Laurent Alric, Laure Swiader, Suzanne Tavitian, Jean-Marc Durand, Sylvie Ollier, Aline Moignet‐Autrel, Karen Delavigne, Miguel Carreiro, Pierre Cougoul, Jean Estelle, Sylvain Audia, Benjamin De Sainte Marie, Veronique Remy, Xavier Delbrel, Samuel Deshayes, Francis Gaches, Helene Hennique, Lorraine Leplay, Gaetan Sauvetre, Antoine Briantais, Cécile Borel, Kamel Laribi, Martin Michaud, Stéphane Cheze, Sondess Hadj‐Khelifa, Guillaume Martin‐Blondel, Geoffrey Urbanski, Brice Castel, Guillaume Moulis, Fanny Nuccio, Soraya Leclerc-Teffahi, Odile Beyne‐Rauzy, Benjamin Hebraud, Aurelie Godel‐Labouret, Pierre Duffau, Sarah Khatibi, Baptiste Andre, Gregory Pugnet, Daniel Adoue, Julie Seguier, Clement Gaudin, Marc Michel, Myriam Aroichane, Laurent Prudhomme, Margaux Lafaurie, Manuela Rueter, Philippe Montane De La Roque, Natacha Brun, Aurelie Saunier, Julie Graveleau, Johanne Germain, Willy Vaillant, Agnès Sommet, Maryse Lapeyre-Mestre, Delphine Bonnet, Stephane Sire, Yann Leveneur, Caroline Soubrier, Alina Danu, Veronique Veit, Patrick Giraud, François Lifermann, Gwenola Maigne, Jean-François Viallard, Clothilde Martel, Nicolas Limal, Delphine Brechemier, Frederique Roy‐Peaud, Serge Madaule, Laurent Sailler, Thibault Comont, Benoit Faucher, Laurent Balardy, Carine Courtault, Claire Dingremont, Jean-Robert Harlé, Sophie Arista, Mikael Ebbo, Bertrand Godeau, Jeremie Dion, Bernard Bonnotte, Irène Machelart, Matthieu Mahévas, Nicolas Schleinitz, Arnaud Saint‐Lezer, Corentin Orvain, Christian Recher, Patrick Rispal, Bertrand Lioger
Publikováno v:
American journal of hematology. 97(2)
Autor:
Antoine Hankard, François Maillot, Gwenola Maigne, Alexandra Audemard-Verger, Achille Aouba, Thierry Lobbedez, Eve Calvar
Publikováno v:
La Revue de Médecine Interne. 41:567-568
Autor:
Gaétane Planchard, Alexandra Audemard-Verger, Achille Aouba, Benjamin Savoye, Maxime Faisant, Evangeline Pillebout, Gwenola Maigne
Publikováno v:
European Journal of Case Reports in Internal Medicine
European Journal of Case Reports in Internal Medicine (2019)
European Journal of Case Reports in Internal Medicine (2019)
Introduction Immunoglobulin A vasculitis (IgAV) is a small-vessel vasculitis with IgA-dominant immune deposits. IgAV frequently involves the skin, gastrointestinal tract, joints and kidneys. In contrast to other types of small-vessel vasculitis, IgAV
Autor:
Samuel Deshayes, Gwenola Maigne, Hubert de Boysson, Thierry Lobbedez, Frédérique Grandhomme, Nicolas Martin Silva, Delphine Mariotte, Kathy Khoy, Achille Aouba, Jonathan Boutemy, Claire Brière-Bellier, Claire Delmas, Boris Bienvenu
Publikováno v:
The Journal of rheumatology. 46(11)
Objective.Deficiency in alpha-1 antitrypsin (AAT) is a possible pathogenic cofactor in antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). However, the clinical effect of AAT deficiency remains poorly established in this setting.
Autor:
Samuel Deshayes, Amélie Seguin, Gwenola Maigne, A. Baldolli, Aurélie Joret, Damien du Cheyron, Audrey Sultan, Nizar Mahlaoui, Boris Bienvenu, Nicolas Martin Silva
Publikováno v:
Infection. 47(1)
Primary immunodeficiency (PID) in adults is rare and mostly revealed by infections. Adults without predisposing factors who were admitted to an intensive care unit (ICU) for infection were screened for PID. Six PID cases were diagnosed, mostly reveal
Autor:
Hubert de Boysson, Jean-Jacques Parienti, Gwenola Maigne, Eric Liozon, Emmanuel Touzé, Nicolas Martin Silva, Maxime Samson, Jonathan Boutemy, Karim Sacre, Kim Heang Ly, Bernard Bonnotte, Achille Aouba, Boris Bienvenu, Delphine Larivière
Publikováno v:
The Journal of rheumatology. 44(3)
Objective.Our aim was to describe patients with giant cell arteritis (GCA)–related stroke and to compare them with a control group of GCA patients without stroke.Methods.We created a retrospective multicenter cohort of patients with (1) GCA diagnos