Zobrazeno 1 - 10
of 324
pro vyhledávání: '"Noémie Jourde Chiche"'
Autor:
Karine Baumstarck, Noémie Jourde-Chiche, Eric Daugas, Marie Himbert, Léa Chapart, Nicolas Charles
Publikováno v:
RMD Open, Vol 10, Iss 2 (2024)
Objectives Discontinuation or continuation of maintenance immunosuppressive therapy (MIST) after a severe lupus nephritis (LN) requires measuring the risk of relapse but reliable clinical and biological markers are lacking. The WIN-IgE study assesses
Externí odkaz:
https://doaj.org/article/598e7182dc5241c8adcccaba4546241a
Autor:
Nathalie Costedoat-Chalumeau, Alexandre Karras, Aurelie Hummel, Veronique Le Guern, Carole Burger, Nicolas Benichou, Céline Narjoz, Noémie Jourde Chiche, Julie Chezel, Éric Thervet, Nicolas Pallet
Publikováno v:
Lupus Science and Medicine, Vol 11, Iss Suppl 1 (2024)
Externí odkaz:
https://doaj.org/article/d7053c2d9e394d4aa7b562fbdcde01e7
Autor:
Thomas Robert, Guillaume Lano, Noémie Resseguier, Mickaël Bobot, Dammar Bouchouareb, Stéphane Burtey, Xavier de Lamballerie, Jean Dhorne, Bertrand Dussol, Ariane Duval, Julien Faraut, Toscane Fourié, Philippe Giaime, Mourad Hallah, Dominique Jaubert, Océane Jéhel, Tristan Legris, Stéphane Liotatis, Valérie Moal, Laetitia Ninove, Nathalie Pedinielli, Marion Pelletier, Manon Romeu-Giannoli, Mariela Saba, Marion Sallée, Laurent Samson, Adriana Saveanu, Violaine Scarfoglière, Pascale Sebahoun, Romain Vial, Clarissa Von Kotze, Philippe Brunet, Gaëtan Lebrun, Stanislas Bataille, Noémie Jourde-Chiche
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-8 (2022)
Abstract Hemodialysis (HD) patients are at risk for severe COVID-19 and cannot comply with social distancing. SARS-COV2 seroprevalence in French patients and caregivers after the first wave of COVID-19 is unknown. SeroCOVIDial is a prospective study
Externí odkaz:
https://doaj.org/article/4a764384b0e14580a19e91dd27912565
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:
Mathilde Fedi, Mickaël Bobot, Julia Torrents, Pierre Gobert, Éric Magnant, Yannick Knefati, David Verhelst, Gaëtan Lebrun, Valérie Masson, Philippe Giaime, Julien Santini, Stanislas Bataille, Philippe Brunet, Bertrand Dussol, Stéphane Burtey, Julien Mancini, Laurent Daniel, Noémie Jourde-Chiche
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-9 (2021)
Abstract Background Few data is available on the risk/benefit balance of native kidney biopsy (KB) in very elderly patients. Methods Multicenter retrospective cohort study in the Aix-Marseille area: the results of KB and medical charts of all patient
Externí odkaz:
https://doaj.org/article/7defd54093a145f3a9c5a3be4a1445c6
Autor:
Maximilien Grall, Florence Daviet, Noémie Jourde Chiche, François Provot, Claire Presne, Jean-Philippe Coindre, Claire Pouteil-Noble, Alexandre Karras, Dominique Guerrot, Arnaud François, Ygal Benhamou, Agnès Veyradier, Véronique Frémeaux-Bacchi, Paul Coppo, Steven Grangé
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-8 (2021)
Abstract Background Gemcitabine is a broadly prescribed chemotherapy, the use of which can be limited by renal adverse events, including thrombotic microangiopathy (TMA). Methods This study evaluated the efficacy of eculizumab, a monoclonal antibody
Externí odkaz:
https://doaj.org/article/67e7866a6eef451f8b16ddf8f9df68a6
Autor:
Benoit Blanchet, Moez Jallouli, Marie Allard, Pascale Ghillani-Dalbin, Lionel Galicier, Olivier Aumaître, François Chasset, Véronique Le Guern, Frédéric Lioté, Amar Smail, Nicolas Limal, Laurent Perard, Hélène Desmurs-Clavel, Du Le Thi Huong, Bouchra Asli, Jean-Emmanuel Kahn, Laurent Sailler, Félix Ackermann, Thomas Papo, Karim Sacré, Olivier Fain, Jérôme Stirnemann, Patrice Cacoub, Gaelle Leroux, Judith Cohen-Bittan, Jérémie Sellam, Xavier Mariette, Claire Goulvestre, Jean Sébastien Hulot, Zahir Amoura, Michel Vidal, Jean-Charles Piette, on behalf of the PLUS Group, Noémie Jourde-Chiche, Nathalie Costedoat-Chalumeau
Publikováno v:
Arthritis Research & Therapy, Vol 22, Iss 1, Pp 1-10 (2020)
Abstract Background Hydroxychloroquine (HCQ) levels can be measured in both serum and whole blood. No cut-off point for non-adherence has been established in serum nor have these methods ever been compared. The aims of this study were to compare thes
Externí odkaz:
https://doaj.org/article/97a679396d2b4973bdad9b082ffe9e45
Autor:
Maëlis Kauffmann, Mickaël Bobot, Laurent Daniel, Julia Torrents, Yannick Knefati, Olivier Moranne, Stéphane Burtey, Christine Zandotti, Noémie Jourde-Chiche
Publikováno v:
BMC Nephrology, Vol 21, Iss 1, Pp 1-8 (2020)
Abstract Background The seroprevalence of human Parvovirus B19 (PVB19) is 70–85% in adults worldwide. PVB19 is the etiologic agent of the fifth disease, is a cause of aplastic anemia, and can be associated with kidney injury. We aimed to describe t
Externí odkaz:
https://doaj.org/article/655f6b6917ad4c7989d89b80a9fc5f4d
Autor:
Florence Daviet, Muriel G. Blin, Karim Fallague, Richard Bachelier, Manon Laforêt, Manon Carré, Stéphane Poitevin, Françoise Dignat-George, Marcel Blot-Chabaud, Nathalie Bardin, Stéphane Burtey, Noémie Jourde-Chiche, Aurélie S. Leroyer
Publikováno v:
Kidney International Reports, Vol 5, Iss 7, Pp 1071-1075 (2020)
Externí odkaz:
https://doaj.org/article/51059cceb933477eb1d1eef5d67c5fef
Autor:
Sophie Greillier, Laurent Daniel, Catherine Caillaud, Bertrand Dussol, Guy Touchard, Jean-Michel Goujon, Noémie Jourde-Chiche, Mickaël Bobot
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-5 (2020)
Abstract Background Fabry disease (FD) is an X-linked lysosomal storage disorder due to deficient alpha-galactosidase activity leading to intracellular glycosphingolipid accumulation. Multiple variants have been reported in the GLA gene coding for al
Externí odkaz:
https://doaj.org/article/32902ced1c8e4bb1bbc4d3d837bed829