Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Pierre-André Jarrot"'
Autor:
Robin Arcani, Louise Rey, Alice Mazziotto, Daniel Bertin, Gilles Kaplanski, Pierre-André Jarrot, Pierre Lafforgue, Geoffroy Venton, Xavier Heim, Patrick Villani, Jean-Louis Mège, Alexandre Brodovitch, Nathalie Bardin
Publikováno v:
Arthritis Research & Therapy, Vol 25, Iss 1, Pp 1-9 (2023)
Abstract Background Anti-Jo-1 autoantibodies represent essential markers in the diagnosis of antisynthetase syndrome (ASS). In this retrospective study, we aimed to investigate whether their concentrations and fluctuations could both respectively ref
Externí odkaz:
https://doaj.org/article/06fbc7f5842245c2b3f6405f5b864165
Autor:
Pierre-André Jarrot, Adrien Mirouse, Sébastien Ottaviani, Simon Cadiou, Jean-Hugues Salmon, Eric Liozon, Simon Parreau, Martin Michaud, Benjamin Terrier, Pierre-Edouard Gavand, Ludovic Trefond, Virginie Lavoiepierre, Jeremy Keraen, Daniel Rekassa, Bastien Bouldoires, Thierry Weitten, Damien Roche, Antoine Poulet, Caroline Charpin, Vincent Grobost, Marion Hermet, Magali Pallure, Chloe Wackenheim, Ludovic Karkowski, Pierre Grumet, Thomas Rogier, Nabil Belkefi, Vincent Pestre, Emilie Broquet, Amélie Leurs, Sophie Gautier, Valérie Gras, Pierre Gilet, Jan Holubar, Nadia Sivova, Nicolas Schleinitz, Jean-Marc Durand, Brice Castel, Alexandre Petrier, Robin Arcani, Baptiste Gramont, Philippe Guilpain, Hubert Lepidi, Pierre-Jean Weiller, Joelle Micallef, David Saadoun, Gilles Kaplanski
Publikováno v:
Human Vaccines & Immunotherapeutics, Vol 20, Iss 1 (2024)
ABSTRACTWe conducted a national in-depth analysis including pharmacovigilance reports and clinical study to assess the reporting rate (RR) and to determine the clinical profile of polymyalgia rheumatica (PMR) and giant cell arteritis (GCA) in COVID-1
Externí odkaz:
https://doaj.org/article/970ddb7d49c04bd4a900d1b8a0d87da2
Autor:
Alice Corthier, Marie Jachiet, Daniel Bertin, Aude Servais, Christelle Barbet, Adrien Bigot, Marie-Sylvie Doutre, Didier Bessis, Ancuta Bouffandeau, Olivier Moranne, Pierre-André Jarrot, Nathalie Bardin, Benjamin Terrier, Stephane Burtey, Xavier Puéchal, Laurent Daniel, Noémie Jourde-Chiche
Publikováno v:
BMC Nephrology, Vol 23, Iss 1, Pp 1-12 (2022)
Abstract Background Hypocomplementemic urticarial vasculitis (HUV) is a rare systemic vasculitis. We aimed to describe the kidney involvement of HUV in a multicenter national cohort with an extended follow-up. Methods All patients with HUV (internati
Externí odkaz:
https://doaj.org/article/a47ebc38314743829b9a693ba7d5459b
Autor:
Hubert de Boysson, Maelle Le Besnerais, Félix Blaison, Aurélie Daumas, Pierre-André Jarrot, François Perrin, Nathalie Tieulié, Alexandre Maria, Pierre Duffau, Bruno Gombert, Maxime Samson, Olivier Espitia, Marc Lambert, Arsène Mékinian, Achille Aouba, for the French Study Group for Large Vessel Vasculitis (GEFA)
Publikováno v:
Arthritis Research & Therapy, Vol 23, Iss 1, Pp 1-7 (2021)
Abstract Objective To assess the efficacy and tolerance of tocilizumab (TCZ) in giant cell arteritis (GCA) patients over 80. Method GCA patients over 80 years old from the French Study Group for Large Vessel Vasculitis register who received TCZ were
Externí odkaz:
https://doaj.org/article/42f1063076c240e6adcacd8abf147a0e
Autor:
Raphael Cauchois, Lea Pietri, Jean-Baptiste Dalmas, Marie Koubi, Thibaut Capron, Nadim Cassir, Nicola Potere, Ildo Polidoro, Rodolphe Jean, Pierre-André Jarrot, Baptiste Andre, Veronique Veit, Julien Carvelli, Vanessa Pauly, Pascal Chanez, Laurent Papazian, Gilles Kaplanski
Publikováno v:
Microorganisms, Vol 10, Iss 12, p 2423 (2022)
During SARS-CoV-2 infection, eosinopenia may reflect a hyperactive immune response. In this study of hospitalized COVID-19 patients, we aimed to better understand the prognostic value of severe eosinopenia (absolute eosinophil count = 0 G/L) and deci
Externí odkaz:
https://doaj.org/article/ab3dfe0a2b6748a29cdd63416d094d0a
Autor:
Romain Vial, Marion Gully, Mickael Bobot, Violaine Scarfoglière, Philippe Brunet, Dammar Bouchouareb, Ariane Duval, He-oh Zino, Julien Faraut, Océane Jehel, Yaël Berdad-Haddad, Stéphane Burtey, Pierre-André Jarrot, Guillaume Lano, Thomas Robert
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 1, p 4 (2020)
Background: Daily management to shield chronic dialysis patients from SARS-CoV-2 contamination makes patient care cumbersome. There are no screening methods to date and a molecular biology platform is essential to perform RT-PCR for SARS-CoV-2; howev
Externí odkaz:
https://doaj.org/article/bd0269df2c74461a972291ba34067989
Autor:
Pierre-André Jarrot, Gilles Kaplanski
Publikováno v:
Mediators of Inflammation, Vol 2014 (2014)
TNF-α is a pleiotropic cytokine, which plays a major role in the pathogenesis of numerous autoimmune and/or inflammatory systemic diseases. Systemic vasculitis constitutes a group of rare diseases, characterized by inflammation of the arterial or ve
Externí odkaz:
https://doaj.org/article/0c7444e1c99f49568999572a01bd7903
Autor:
Quentin Gomes de Pinho, Aurélie Daumas, Audrey Benyamine, Julien Bertolino, Mikaël Ebbo, Nicolas Schleinitz, Jean-Robert Harlé, Pierre André Jarrot, Gilles Kaplanski, Julie Berbis, Mohamed Boucekine, Pascal Rossi, Brigitte Granel
Publikováno v:
JCR: Journal of Clinical Rheumatology. 29:e25-e31
Autor:
Quentin Gomes de Pinho, Aurélie Daumas, Audrey Benyamine, Julien Bertolino, Pascal Rossi, Nicolas Schleinitz, Jean-Robert Harlé, Pierre André Jarrot, Gilles Kaplanski, Julie Berbis, Brigitte Granel
Publikováno v:
Rheumatology International. 42:2013-2018
Giant cell arteritis (GCA) is the most frequent vasculitis affecting adults aged 50 years. Cardiac involvement in GCA is considered rare, and only a few cases of pericarditis have been reported. The aim of this study was to determine the characterist
Autor:
Thomas Escoda, Julia George, Pierre-André Jarrot, Rodolphe Jean, Karin Mazodier, Frederick Sanderson, Pascale Poullin, Ludivine Saby, Noémie Jourde-Chiche, Gilles Kaplanski, Laurent Chiche
Publikováno v:
Lupus. 31:744-753
Aortitis is a classic manifestation of large vessel vasculitis. Antiphospholipid syndrome (APS), sometimes known as Hughes syndrome, is an acquired autoimmune disorder that manifests clinically as recurrent venous or arterial thrombosis. Patients wit