Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Thomas Quemeneur"'
Autor:
Romain Dubois, Sébastien Puigrenier, Sabine Tricot, Jean-Baptiste Gibier, Thomas Quemeneur, M. Ulrich, G. Collet, Viviane Gnemmi
Publikováno v:
Néphrologie & Thérapeutique. 16:372-375
Resume Le lymphome intravasculaire est une forme rare de lymphome non hodgkinien a grandes cellules B, de presentation clinique heterogene et de diagnostic histologique difficile. Dans ce contexte, l’interet diagnostique de la tomographie par emiss
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:
Fabien Koskas, Patrice Cacoub, Eric Hachulla, Hélène Maillard, Marc Lambert, Thomas Quemeneur, Alexandre Le Joncour, S. Soudet, Cécile Yelnik, David Saadoun
Publikováno v:
Angiology. 71:621-625
Thromboangiitis obliterans (TAO) is an inflammatory disease that usually affects small and medium-sized arteries in the upper and lower limbs of young smokers. Previous studies showed that the spectrum TAO has changed in the 80s: the male-to-female r
Autor:
Benjamin Terrier, Raphaël Darbon, Cécile-Audrey Durel, Eric Hachulla, Alexandre Karras, Hélène Maillard, Thomas Papo, Xavier Puechal, Grégory Pugnet, Thomas Quemeneur, Maxime Samson, Camille Taille, Loïc Guillevin, Collaborators
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-1 (2021)
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-1 (2021)
An amendment to this paper has been published and can be accessed via the original article.
Autor:
Antoine Lafarge, Mohamed Hamidou, Matthieu Groh, Pacal Cohen, Alexandre Karras, Christian Pagnoux, Camillo Ribi, Xavier Puéchal, Benjamin Terrier, Luc Mouthon, Thomas Quemeneur, Loïc Guillevin, Maxime Samson, Adrien Joseph
Publikováno v:
Annals of the Rheumatic Diseases. 79:431-433
Reduction in cyclophosphamide cumulative dose and introduction of newer immunosuppressive drugs may reduce the malignant burden of systemic necrotising vasculitis (SNV).1 2 This study aimed to describe malignancies recorded in five randomised control
Autor:
Marie-Christine Copin, Thierry Martin, Guillaume Lefèvre, Matthieu Groh, Jean-Baptiste Gibier, Marc Lambert, François Pontana, Pierre-Yves Hatron, Myriam Labalette, Jean-François Viallard, Delphine Staumont-Sallé, F. Dezoteux, Chafika Morati-Hafsaoui, Eric Hachulla, Benjamin Lopez, Pascal DeGroote, Thomas Quemeneur, Jean-Emmanuel Kahn, Mohamed Hamidou, Amélie Leurs, Louis Terriou, Nicolas Etienne, Cécile Chenivesse, David Launay, Nicolas Schleinitz
Publikováno v:
The Journal of Allergy and Clinical Immunology: In Practice
The Journal of Allergy and Clinical Immunology: In Practice, 2020, 8 (4), pp.1329-1340.e3. ⟨10.1016/j.jaip.2019.12.011⟩
The Journal of Allergy and Clinical Immunology: In Practice, 2020, 8 (4), pp.1329-1340.e3. ⟨10.1016/j.jaip.2019.12.011⟩
International audience; Background: The absence of asthma may rule out a diagnosis of eosinophilic granulomatosis with polyangiitis in patients with hypereosinophilic syndrome (HES) and features of vasculitis.Objective: To describe eosinophilic vascu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::717b9236b1de8a8b308a5d9e9df49574
https://hal.science/hal-03869830
https://hal.science/hal-03869830
Autor:
Dimitri Titeca-Beauport, Vincent Audard, Laurent Juillard, Marie-Noëlle Peraldi, Jean-François Subra, Eric Thervet, Jean-Michel Halimi, Thierry Lobbedez, Gabriel Choukroun, Mathilde Tamain, Marc Hazzan, Alexandre Ganea, Maité Daroux, Thomas Quemeneur, Dominique Guerrot, Pauline Caillard, Marie Essig, François Vrtovsnik, Jean-Michel Rebibou, Cécile Vigneau, R. Makdassi, Marion Rabant, Morgane Heitz, Vincent Vuiblet, Alexandre Hertig, Adnane Lamrani
Publikováno v:
Journal of Clinical Medicine
Journal of Clinical Medicine, 2020, 9 (3), pp.698. ⟨10.3390/jcm9030698⟩
Journal of Clinical Medicine, MDPI, 2020, 9 (3), pp.698. ⟨10.3390/jcm9030698⟩
Journal of Clinical Medicine, Vol 9, Iss 3, p 698 (2020)
Volume 9
Issue 3
Journal of Clinical Medicine, 2020, 9 (3), pp.698. ⟨10.3390/jcm9030698⟩
Journal of Clinical Medicine, MDPI, 2020, 9 (3), pp.698. ⟨10.3390/jcm9030698⟩
Journal of Clinical Medicine, Vol 9, Iss 3, p 698 (2020)
Volume 9
Issue 3
In patients presenting with anti-glomerular basement membrane (GBM) disease with advanced isolated kidney involvement, the benefit of intensive therapy remains controversial due to adverse events, particularly infection. We aim to describe the burden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be29c3daa88cebea92dd6012c54246f7
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02796989/document
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02796989/document
Autor:
Nicolas Wayolle, Marie Frimat, Claude-Alain Maurage, François Glowacki, Philippe Vanhille, Jean-Baptiste Gibier, Jérôme Verine, Cyrille Vandenbussche, Sarah Humez, Nassima Ramdane, Carole Cordonnier, Thomas Quemeneur, Pierre-Yves Hatron, Laura Bitton, Evelyne Mac Namara, Pierre Bataille, David Buob, Raymond Azar, Marie-Christine Copin, Viviane Gnemmi, Rémi Lenain, Michael Perrais
Publikováno v:
Journal of nephrology. 33(4)
The aims of this study were to determine whether tubulointerstitial damage in the form of interstitial fibrosis/tubular atrophy and total interstitial inflammation predicted progression to end stage renal disease (ESRD) and/or renal relapse (RR) in p
Autor:
Camille Francès, Christophe Deligny, Bernard Imbert, Emmanuel Chatelus, L. Boukari, Noémie Le Gouellec, Claire Cazalets, Patricia Senet, Arsène Mekinian, Thierry Martin, Patrick Jego, Christian Agard, Thomas Quemeneur, David Launay, Pierre-Yves Hatron, Alexis Mathian, Sébastien Rivière, Alain Le Quellec, Alban Deroux, Grégory Pugnet, Alain Lescoat, Thomas Sené, Silvia Speca, Olivier Fain, Sébastien Sanges, Eric Hachulla, Sylvain Dubucquoi
Publikováno v:
Autoimmunity Reviews
Autoimmunity Reviews, 2017, 16 (4), pp.377-384. ⟨10.1016/j.autrev.2017.02.008⟩
Autoimmunity Reviews, Elsevier, 2017, 16 (4), pp.377-384. ⟨10.1016/j.autrev.2017.02.008⟩
Autoimmunity Reviews, 2017, 16 (4), pp.377-384. ⟨10.1016/j.autrev.2017.02.008⟩
Autoimmunity Reviews, Elsevier, 2017, 16 (4), pp.377-384. ⟨10.1016/j.autrev.2017.02.008⟩
International audience; BACKGROUND:As intravenous immunoglobulins (IVIG) exhibit immunomodulatory and antifibrotic properties, they may be a relevant treatment for systemic sclerosis (SSc). The objectives of this work were thus to report on the effic
Autor:
Gerard Cardon, Jean-Dominique Gheerbrant, Laura Bitton, Pierre-Yves Hatron, François Glowacki, Eric Auxenfants, Maxime Hoffmann, Thomas Quemeneur, Pierre Bataille, Raymond Azar, Cyrille Vandenbussche, Evelyne Macnamara, Viviane Gnemmi
Publikováno v:
American journal of nephrology. 49(6)
Background: Pauci-immune glomerulonephritis (PIGN) is a major prognostic factor in antineutrophil cytoplasmic antibodies-associated vasculitis (AAV). Renal remission is usually defined as improvement or stabilization of serum creatinine and proteinur