Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Nathalie Quellard"'
Autor:
Samih H. Nasr, Julie A. Vrana, Surendra Dasari, Frank Bridoux, Mary E. Fidler, Sihem Kaaki, Nathalie Quellard, Alexia Rinsant, Jean Michel Goujon, Sanjeev Sethi, Fernando C. Fervenza, Lynn D. Cornell, Samar M. Said, Ellen D. McPhail, Loren P. Herrera Hernandez, Joseph P. Grande, Marie C. Hogan, John C. Lieske, Nelson Leung, Paul J. Kurtin, Mariam P. Alexander
Publikováno v:
Kidney International Reports, Vol 3, Iss 1, Pp 56-64 (2018)
Fibrillary glomerulonephritis (FGN) is a rare disease with unknown pathogenesis and a poor prognosis. Until now, the diagnosis of this disease has required demonstration of glomerular deposition of randomly oriented fibrils by electron microscopy tha
Externí odkaz:
https://doaj.org/article/5a6bfb80b6b44dfca60e41125f0467d5
Autor:
Agnieszka A Pozdzik, Laetitia Giordano, Gang Li, Marie-Hélène Antoine, Nathalie Quellard, Julie Godet, Eric De Prez, Cécile Husson, Anne-Emilie Declèves, Volker M Arlt, Jean-Michel Goujon, Isabelle Brochériou-Spelle, Steven R Ledbetter, Nathalie Caron, Joëlle L Nortier
Publikováno v:
PLoS ONE, Vol 11, Iss 7, p e0157288 (2016)
The platelet-derived growth factor receptor β (PDGFRβ)+ perivascular cell activation becomes increasingly recognized as a main source of scar-associated kidney myofibroblasts and recently emerged as a new cellular therapeutic target.In this regard,
Externí odkaz:
https://doaj.org/article/07b8811d1541456db53d3a10f29a385a
Autor:
Martine Fanton d'Andon, Nathalie Quellard, Béatrice Fernandez, Gwenn Ratet, Sonia Lacroix-Lamandé, Alain Vandewalle, Ivo G Boneca, Jean-Michel Goujon, Catherine Werts
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 8, Iss 1, p e2664 (2014)
BACKGROUND: Leptospira (L.) interrogans are bacteria responsible for a worldwide reemerging zoonosis. Rodents carry L. interrogans asymptomatically in their kidneys and excrete bacteria in the urine, contaminating the environment. Humans get infected
Externí odkaz:
https://doaj.org/article/813a9a58a7be4327af64203597362c63
Autor:
Vanessa, Barbot, Virginie, Migeot, Nathalie, Quellard, Marie-Hélène, Rodier, Christine, Imbert
Publikováno v:
In Water Research 1 November 2012 46(17):5707-5714
Autor:
David Malka, Alexis Mathian, Olivier Lambotte, Hassan Izzedine, Zahir Amoura, Andrea Varga, Sihem Kaaki, Christine Mateus, Alexandra Leary, Jean-Charles Soria, Isabelle Brocheriou, Aurélien Marabelle, Stéphane Champiat, Jean-Michel Goujon, Emilie Routier, Cécile Picard, Nathalie Quellard, Judith Michels, Jean-Marie Michot
Publikováno v:
Clinical Kidney Journal
Clinical Kidney Journal, 2019, 12 (1), pp.81-88. ⟨10.1093/ckj/sfy100⟩
Clinical Kidney Journal, Oxford University Press, 2019, 12 (1), pp.81-88. ⟨10.1093/ckj/sfy100⟩
Clinical Kidney Journal, 2019, 12 (1), pp.81-88. ⟨10.1093/ckj/sfy100⟩
Clinical Kidney Journal, Oxford University Press, 2019, 12 (1), pp.81-88. ⟨10.1093/ckj/sfy100⟩
International audience; Objective : Expanded clinical experience with patients treated by pembrolizumab has accumulated. However, renal toxicities associated with this anti-programmed cell death 1 agent are poorly described because kidney histology i
Autor:
Estelle Desport, Vincent Javaugue, Antoine Durrbach, Didier Samuel, Frank Bridoux, Magali Colombat, Nathalie Quellard, S. Valleix, Thierry Frouget, Jean Philippe Rerolle, Jean-Claude Aldigier, Pierre-Raphaël Rothschild, Caroline Beugnet, Antoine P. Brézin, Nathalie Rioux-Leclercq, Aurélien Tiple, François Paraf, Jean-Michel Goujon
Publikováno v:
Kidney International
Kidney International, 2020, 98 (1), pp.195-208. ⟨10.1016/j.kint.2020.03.033⟩
Kidney International, Nature Publishing Group, 2020, 98 (1), pp.195-208. ⟨10.1016/j.kint.2020.03.033⟩
Kidney International, 2020, 98 (1), pp.195-208. ⟨10.1016/j.kint.2020.03.033⟩
Kidney International, Nature Publishing Group, 2020, 98 (1), pp.195-208. ⟨10.1016/j.kint.2020.03.033⟩
International audience; Apolipoprotein A1 amyloidosis (ApoAI) results from specific mutations in the APOA1 gene causing abnormal accumulation of amyloid fibrils in diverse tissues. The kidney is a prominent target tissue in ApoAI amyloidosis with a r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dcd8d55f01a3b13d0f19dff34b13181
https://hal.science/hal-03228634/file/S0085253820304178.pdf
https://hal.science/hal-03228634/file/S0085253820304178.pdf
Autor:
I. Bouteau, Jean-Paul Fermand, J. Diolez, Nathalie Quellard, A. Colombo, Arnaud Jaccard, Jean-Michel Goujon, L. Ecotière, Frank Bridoux, Christophe Sirac, Vincent Javaugue, Estelle Desport, Guy Touchard
Publikováno v:
La Revue De Médecine Interne
La Revue De Médecine Interne, Elsevier, 2018, 39 (3), pp.161-170. ⟨10.1016/j.revmed.2017.03.012⟩
La Revue De Médecine Interne, Elsevier, 2018, 39 (3), pp.161-170. ⟨10.1016/j.revmed.2017.03.012⟩
Two categories of renal disorders associated with monoclonal gammopathies are to be distinguished, according to the characteristics of the underlying B-cell clone. The first group of renal diseases always occurs in the setting of high tumor mass with
Autor:
Loren P. Herrera Hernandez, Ellen D. McPhail, Julie A. Vrana, Alexia Rinsant, Frank Bridoux, Samih H. Nasr, Nelson Leung, Surendra Dasari, Joseph P. Grande, Fernando C. Fervenza, Mariam P. Alexander, Paul J. Kurtin, Jean Michel Goujon, Sanjeev Sethi, Lynn D. Cornell, Samar M. Said, Marie C. Hogan, Mary E. Fidler, Sihem Kaaki, John C. Lieske, Nathalie Quellard
Publikováno v:
Kidney International Reports, Vol 3, Iss 1, Pp 56-64 (2018)
Kidney International Reports
Kidney International Reports
Introduction Fibrillary glomerulonephritis (FGN) is a rare disease with unknown pathogenesis and a poor prognosis. Until now, the diagnosis of this disease has required demonstration of glomerular deposition of randomly oriented fibrils by electron m
Publikováno v:
Microbes and Infection
Microbes and Infection, Elsevier, 2017, 19 (4-5), pp.259-266. ⟨10.1016/j.micinf.2016.12.005⟩
Microbes and Infection, Elsevier, 2017, 19 (4-5), pp.259-266. ⟨10.1016/j.micinf.2016.12.005⟩
International audience; Klebsiella pneumoniae is a bacterium that can be in relation with free living amoebae like Acanthamoeba castellanii in natural environments such as soil and water. This pathogen, which is responsible for community-acquired pne
Autor:
Alexia Rinsant, Christelle Oblet, Agnès Paquet, Sihem Kaaki, Michel Cogné, Nathalie Quellard, Arnaud Jaccard, François Boyer, Amélie Bonaud, Christophe Sirac, Bastien Hervé, Guy Touchard, Mohamad Omar Ashi, Vincent Javaugue, Claire Carrion, Nicolas Pons, Maria Victoria Ayala, Sébastien Bender, Frank Bridoux, Laurent Delpy, Zeliha Oruc
Light chain deposition disease (LCDD) is a rare disorder characterized by glomerular and peritubular amorphous deposits of a monoclonal immunoglobulin (Ig) light chain (LC), leading to nodular glomerulosclerosis and nephrotic syndrome. We developed a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40ad088a254525c5f71e4e14896f6d55