Zobrazeno 1 - 10
of 88
pro vyhledávání: '"Antoine Huart"'
Autor:
Yves Renaudineau, Dominique Chauveau, Stanislas Faguer, Antoine Huart, David Ribes, Gregory Pugnet, Laurent Sailler, Thibaut Jamme, Emmanuel Treiner, Françoise Fortenfant, Chloé Bost, Caroline Carlé, Julie Belliere
Publikováno v:
Journal of Translational Autoimmunity, Vol 9, Iss , Pp 100244- (2024)
Lupus nephritis (LN) diagnosis and follow-up requires noninvasive biomarkers. Therefore, the added value of coupling the urinary soluble (s)CD163/creatinuria ratio with serological markers was evaluated in a real-world clinical practice. To this end,
Externí odkaz:
https://doaj.org/article/31c468b83bbc4016992755a3f69cd700
Autor:
Alexis Talbot, Arthur Bobin, Léa Tabone, Jérôme Lambert, Catherine Boccaccio, Cécile Deal, Marie-Odile Petillon, Olivier Allangba, Philippe Agape, Pierre Arnautou, Rakiba Belkhir, Sylvie Cailleres, Driss Chaoui, Marie-Lorraine Chrétien, Olivier Decaux, Samantha Schulmann, Laurent Frenzel, Lauris Gastaud, Antoine Huart, Cyrille Hulin, Lionel Karlin, Kamel Laribi, Ronan Le Calloch, Pascal Lenain, Margaret Macro, Salomon Manier, Lydia Montes, Stéphane Moreau, Philippe Moreau, Véronique Morel, James Norwood, Frédérique Orsini Piocelle, Aurore Perrot, Gian Matteo Pica, Philippe Rey, Anna Schmitt, Anne-Marie Stoppa, Mourad Tiab, Cyrille Touzeau, Valérie Vidal, Marguerite Vignon, Laure Vincent, Zoé Van De Wyngaert, Charles Zarnitsky, Naima Kerbouche, Prani Paka, Xavier Leleu, Bertrand Arnulf, Hervé Avet-Loiseau, IFM: Intergroupe Francophone du Myélome
Publikováno v:
Haematologica, Vol 108, Iss 10 (2023)
Belantamab mafodotin (BM) is an anti-BCMA antibody-drug conjugate (GSK2857916) that represents an alternative option in multiple myeloma. We sought to assess the efficacy and safety of BM in a real-world setting in patients who benefited from an earl
Externí odkaz:
https://doaj.org/article/b1c5d27182c748cbbd625be53da24488
Autor:
Sébastien De Almeida Chaves, Tiphaine Porel, Mickael Mounié, Laurent Alric, Léonardo Astudillo, Antoine Huart, Olivier Lairez, Martin Michaud, Grégoire Prévot, David Ribes, Laurent Sailler, Francis Gaches, Daniel Adoue, Gregory Pugnet
Publikováno v:
Arthritis Research & Therapy, Vol 23, Iss 1, Pp 1-12 (2021)
Highlights • Male sex, cardiac involvement, DLCO 5 mg/l are strong predictors of mortality in systemic sclerosis. • This study shows the survival of subtypes and in particular sine scleroderma. • Sine scleroderma subtype has better survival tha
Externí odkaz:
https://doaj.org/article/ff143c860c8840ddbb4d5983ae8e82dd
Autor:
Magali Colombat, Margot Gaspard, Mylène Camus, Jessica Dalloux-Chioccioli, Audrey Delas, Elsa Poullot, Anissa Moktefi, Arnaud François, Anne Moreau, Jean-Bapiste Gibier, Pierre Raynaud, Antoine Huart, Alexis Piedrafita, Julia Gilhodes, Olivier Lairez, Gilles Grateau, Sophie Georgin-Lavialle, Hervé Maisonneuve, Philippe Moreau, Arnaud Jaccard, Franck Bridoux, Violaine Plante-Bordeneuve, Thibaud Damy, Hervé Mal, Pierre Brousset, Sophie Valleix, Odile Burlet-Schiltz
Publikováno v:
Haematologica, Vol 107, Iss 12 (2022)
Externí odkaz:
https://doaj.org/article/f3b5063bec4b4362842350ea0269c2e9
Autor:
Anna Gouin, David Ribes, Magali Colombat, Dominique Chauveau, Gregoire Prevot, Olivier Lairez, Gregory Pugnet, Veronique Fremeaux-Bacchi, Antoine Huart, Julie Belliere, Stanislas Faguer
Publikováno v:
Kidney International Reports, Vol 6, Iss 4, Pp 1015-1021 (2021)
Introduction: Connective tissue diseases, including systemic sclerosis and idiopathic inflammatory myopathies (IIMs), are a very rare cause of thrombotic microangiopathies (TMAs). Whether dysregulation of the complement pathways underlies these secon
Externí odkaz:
https://doaj.org/article/d59fc071c2964faea9af9a48d73439d8
Autor:
Daniel Dang, Pauline Fournier, Eve Cariou, Antoine Huart, David Ribes, Pascal Cintas, Murielle Roussel, Magali Colombat, Yoan Lavie‐Badie, Didier Carrié, Michel Galinier, Olivier Lairez
Publikováno v:
ESC Heart Failure, Vol 7, Iss 5, Pp 2418-2430 (2020)
Abstract Aims Advances have been made over the last decade in the management of cardiac amyloidosis (CA), but a delayed diagnosis is still common. The aim of this study was to describe the journey to CA diagnosis from initial clinical and to analyse
Externí odkaz:
https://doaj.org/article/0c0dc722f6cb45069a50ef29d886029a
Autor:
Eve Cariou, Kevin Sanchis, Khailène Rguez, Virginie Blanchard, Stephanie Cazalbou, Pauline Fournier, Antoine Huart, Murielle Roussel, Pascal Cintas, Michel Galinier, Didier Carrié, Philippe Maury, Yoan Lavie-Badie, Olivier Lairez
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Background: Atrial arrhythmia (AA) is common among patients with cardiac amyloidosis (CA), who have an increased risk of intracardiac thrombus. The aim of this study was to explore the prognostic impact of vitamin K-antagonists (VKA) and direct oral
Externí odkaz:
https://doaj.org/article/435fa4c4080545f590084dc89085847d
Autor:
Alexis Piedrafita, François Vergez, Julie Belliere, Nais Prades, Magali Colombat, Antoine Huart, Jean-Baptiste Rieu, Stéphanie Lagarde, Arnaud Del Bello, Nassim Kamar, Dominique Chauveau, Camille Laurent, Lucie Oberic, Loïc Ysebaert, David Ribes, Stanislas Faguer
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 3, p 604 (2022)
Large granular T-cell leukemia is a clonal hematological condition often associated with autoimmune disorders. Whether small-sized T-cell clones that are otherwise asymptomatic can promote immune kidney disorders remains elusive. In this monocentric
Externí odkaz:
https://doaj.org/article/8818cbf78f84423587d37ac3457ed78f
Autor:
Eloïse Colliou, Alexandre Karras, Jean-Jacques Boffa, David Ribes, Cyril Garrouste, Moglie Le Quintrec, Eric Daugas, Antoine Huart, Didier Ducloux, Aurélie Hummel, Inès Ferrandiz, Nathalie Demoulin, Noémie Jourde-Chiche, Dominique Chauveau, Vincent Audard, Stanislas Faguer
Publikováno v:
Journal of Clinical Medicine, Vol 8, Iss 3, p 298 (2019)
Because of its rarity, renal presentation and outcomes of idiopathic nephrotic syndrome (INS; minimal changes disease or focal and segmental glomerulosclerosis) has poorly been described in elderly patients, precluding an individualized therapy proce
Externí odkaz:
https://doaj.org/article/d9c9bfbb2df34c5bb58e8a7ebb7ac48d
Autor:
Ouadii, Abakarim, Pauline, Condom, Sophie, Voisin, Antoine, Huart, Aurore, Perrot, Teresa, Botin
Publikováno v:
Plasmatology; 1/3/2024, Vol. 18, p1-4, 4p