Zobrazeno 1 - 10
of 99
pro vyhledávání: '"Julie Graveleau"'
Autor:
Hubert de Boysson, Marie Cuchet, Charles Cassius, Pierre Cuchet, Christian Agard, Alexandra Audemard-Verger, Sylvain Marchand-Adam, Raphaëlla Cohen-Sors, Laure Gallay, Julie Graveleau, Cécile Lesort, Kim Ly, Alain Meyer, Grégoire Monseau, Antoine Néel, Bernard Bonnotte, Laurent Pérard, Nicolas Schleinitz, Delphine Mariotte, Brigitte Le Mauff, Gwladys Bourdenet, Wafa Masmoudi, Samuel Deshayes, Anaël Dumont, Anne Dompmartin, Diane Kottler, Achille Aouba
Publikováno v:
Frontiers in Immunology, Vol 14 (2024)
IntroductionThis study aimed to provide an updated analysis of the different prognostic trajectories of patients with anti-melanoma differentiation-associated gene 5 (MDA5) antibodies.MethodsAmong a cohort of 70 patients, baseline characteristics and
Externí odkaz:
https://doaj.org/article/e6e426ae52284ffda7e09c0923a85de4
Autor:
Romain Muller, Paul Habert, Mikael Ebbo, Julie Graveleau, Mathieu Groh, David Launay, Sylvain Audia, Gregory Pugnet, Fleur Cohen, Antoinette Perlat, Audrey Benyamine, Boris Bienvenu, Lea Gaigne, Pascal Chanez, Jean Yves Gaubert, Nicolas Schleinitz
Publikováno v:
European Respiratory Review, Vol 30, Iss 162 (2021)
Objective Immunoglobulin G4-related disease (IgG4-RD) is a rare orphan disease. Lung, pleura, pericardium, mediastinum, aorta and lymph node involvement has been reported with variable frequency and mostly in Asian studies. The objective of this stud
Externí odkaz:
https://doaj.org/article/90c9ecc529364b0691a12a0db0bbaee5
Autor:
Donatienne de Mornac, Christian Agard, Jean-Benoit Hardouin, Mohamed Hamidou, Jérôme Connault, Agathe Masseau, Alexandra Espitia-Thibault, Mathieu Artifoni, Chan Ngohou, François Perrin, Julie Graveleau, Cécile Durant, Pierre Pottier, Antoine Néel, Olivier Espitia
Publikováno v:
Therapeutic Advances in Musculoskeletal Disease, Vol 13 (2021)
Aims: To identify factors associated with vascular events in patients with giant cell arteritis (GCA). Methods: We performed a retrospective study of GCA patients diagnosed over a 20-year-period, who all underwent vascular imaging evaluation at diagn
Externí odkaz:
https://doaj.org/article/c03160e106c247a4816f0aeaca533692
Autor:
Donatienne de Mornac, Olivier Espitia, Antoine Néel, Jérôme Connault, Agathe Masseau, Alexandra Espitia-Thibault, Mathieu Artifoni, Aurélie Achille, Anaïs Wahbi, Mathieu Lacou, Cécile Durant, Pierre Pottier, François Perrin, Julie Graveleau, Mohamed Hamidou, Jean-Benoit Hardouin, Christian Agard
Publikováno v:
Therapeutic Advances in Musculoskeletal Disease, Vol 13 (2021)
Background: Giant cell arteritis (GCA) is the most common systemic vasculitis. Relapses are frequent. The aim of this study was to identify relapse risk factors in patients with GCA with complete large-vessel imaging at diagnosis. Methods: Patients w
Externí odkaz:
https://doaj.org/article/2511d7a149e9492aa2caed9f607904d9
Autor:
Arthur Renaud, Aurélie Caristan, Amélie Seguin, Christian Agard, Gauthier Blonz, Emmanuel Canet, Marion Eveillard, Pascal Godmer, Julie Graveleau, Marie Lecouffe-Desprets, Hervé Maisonneuve, François Perrin, Mohamed Hamidou, Antoine Néel
Publikováno v:
PLoS ONE, Vol 16, Iss 11 (2021)
Background Immune-mediated thrombotic thrombocytopenic purpura (iTTP) is a rare life-threatening thrombotic microangiopathy requiring urgent therapeutic plasma exchange (TPE). However, the exact impact of a slight delay in TPE initiation on the subse
Externí odkaz:
https://doaj.org/article/93ec5618b3fd4c6182ed87fcfa769cac
Autor:
Marion Delplanque, Achille Aouba, Pierre Hirsch, Pierre Fenaux, Julie Graveleau, Florent Malard, Damien Roos-Weil, Nabil Belfeki, Louis Drevon, Artem Oganesyan, Matthieu Groh, Matthieu Mahévas, Jerome Razanamahery, Gwenola Maigne, Matthieu Décamp, Sébastien Miranda, Thomas Quemeneur, Julien Rossignol, Laurent Sailler, Marie Sébert, Louis Terriou, Anna Sevoyan, Yervand Hakobyan, Sophie Georgin-Lavialle, Arsène Mekinian
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 23, p 5586 (2021)
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, exhibits an overlap of clin
Externí odkaz:
https://doaj.org/article/526d406d0fcd4171afde0b4770baee51
Autor:
Raphael Borie, Marie Pierre Debray, Alexis F. Guedon, Arsene Mekinian, Louis Terriou, Valentin Lacombe, Estibaliz Lazaro, Aurore Meyer, Alexis Mathian, Samuel Ardois, Guillaume Vial, Thomas Moulinet, Benjamin Terrier, Yvan Jamilloux, Mael Heiblig, Jean-David Bouaziz, Eve Zakine, Roderau Outh, Sylvie Groslerons, Adrien Bigot, Edouard Flamarion, Marie Kostine, Pierrick Henneton, Sebastien Humbert, Arnaud Constantin, Maxime Samson, Nadine Magy Bertrand, Pascal Biscay, Celine Dieval, Herve Lobbes, Juliette Jeannel, Amelie Servettaz, Leo Adelaide, Julie Graveleau, Benjamin de Sainte-Marie, Joris Galland, Vivien Guillotin, Eugénie Duroyon, Marie Templé, Rim Bourguiba, Sophie Georgin Lavialle, Olivier Kosmider, Alexandra Audemard-Verger, Julien Haroche, Zahir Amoura, Micheline Pha, Miguel Hie, Kilifa Meghit, Murielle Rondeau-Lutz, Jean-Christophe Weber
Publikováno v:
Chest. 163:575-585
The vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome is a newly identified autoinflammatory disorder related to somatic UBA1 mutations. Up to 72% of patients may show lung involvement.What are the pleuropulmonary manifestatio
Autor:
Laura Perray, Yann Nguyen, Gaëlle Clavel Refregiers, Thibaud Chazal, Emmanuel Héron, Clara Pouchelon, Bertrand Dunogué, Nathalie Costedoat-Chalumeau, Anne Murarasu, Alexis Régent, Xavier Puéchal, Benjamin Thoreau, François Lifermann, Julie Graveleau, Miguel Hié, Antoine Froissart, Antoine Baudet, Alban Deroux, Christian Lavigne, Sébastien Puigrenier, Rafik Mesbah, Thomas Moulinet, Claire Vasco, Sabine Revuz, Grégory Pugnet, Virginie Rieu, Anaïs Combes, Antoine Brézin, Benjamin Terrier
Publikováno v:
Rheumatology.
Objectives To describe characteristics, treatment, and outcome of isolated antineutrophil cytoplasm antibody (ANCA)-associated scleritis at diagnosis, in comparison with idiopathic scleritis with negative ANCA tests. Methods This retrospective case c
Autor:
Juliette Demortier, Mathieu Vautier, Olivier Chosidow, Laure Gallay, Didier Bessis, Alice Berezne, Nadège Cordel, Jean Schmidt, Amar Smail, Pierre Duffau, Marie Jachiet, Edouard Begon, Jeremy Gottlieb, François Chasset, Julie Graveleau, Myriam Marque, Elise Cesbron, Amandine Forestier, Séverine Josse, Nicolas Kluger, Caroline Beauchêne, Yannick Le Corre, Valentine Pagis, Aude Rigolet, Perrine Guillaume-Jugnot, François-Jérôme Authier, Nelly Guilain, Nathalie Streichenberger, Sarah Leonard-Louis, Samia Boussouar, Océane Landon-Cardinal, Olivier Benveniste, Yves Allenbach
Publikováno v:
Rheumatology.
Objective Among specific autoantibodies in DM, the anti–small ubiquitin-like modifier activating enzyme (SAE) antibody is rare. We aim to describe the clinical characteristics, cancer prevalence, and muscle pathology of anti-SAE–positive DM. Meth
Autor:
Thibault Comont, Amandine Dernoncourt, Antoinette Perlat, Stéphane Cheze, Bernard Bonnotte, O. Souchaud-Debouverie, Pierre-Yves Jeandel, Bertrand Godeau, Jean-François Viallard, Jean-Christophe Lega, Delphine Gobert, Marc Michel, Mikael Ebbo, Corentin Orvain, Julie Graveleau, Antoine Dossier, Nathalie Costedoat-Chalumeau, Marc Ruivard, Louis Terriou, Arthur Mageau
Publikováno v:
American Journal of Hematology
American Journal of Hematology, 2022, 97 (1), pp.10-17. ⟨10.1002/ajh.26378⟩
American Journal of Hematology, 2022, 97 (1), pp.10-17. ⟨10.1002/ajh.26378⟩
Although splenectomy is still considered the most effective curative treatment for immune thrombocytopenia (ITP), its use has significantly declined in the last decade, especially since the approval of thrombopoietin receptor agonists (TPO-RAs). The