High Resolution Melt analysis for mutation screening in <it>PKD1 </it>and <it>PKD2 </it>

Por Fontes Michel, Berland Yvon, Bataille Stanislas, Burtey Stéphane
Publicado em 2011-10-01

Ascorbic Acid and Gene Expression: Another Example of Regulation of Gene Expression by Small Molecules?

Por Belin, Sophie, Kaya, Ferdinand, Burtey, Stéphane, Fontes, Michel
Publicado em 2010

High Resolution Melt analysis for mutation screening in PKD1 and PKD2

Por Bataille, Stanislas, Berland, Yvon, Fontes, Michel, Burtey, Stéphane
Publicado em 2011

Alternative Splicing Events Is Not a Key Event for Gene Expression Regulation in Uremia

Por Sallée, Marion, Fontès, Michel, Louis, Laurence, Cérini, Claire, Brunet, Philippe, Burtey, Stéphane
Publicado em 2013

The Aryl Hydrocarbon Receptor-Activating Effect of Uremic Toxins from Tryptophan Metabolism: A New Concept to Understand Cardiovascular Complications of Chronic Kidney Disease

Por Sallée, Marion, Dou, Laetitia, Cerini, Claire, Poitevin, Stéphane, Brunet, Philippe, Burtey, Stéphane
Publicado em 2014

Hypokalaemia and dysmorphia, is there a link?

Por Burtey, Stéphane, Sternberg, Damien, Nguyen, Karine, Philip, Nicole, Berland, Yvon, Dussol, Bertrand
Publicado no NDT Plus (2009)

Hepatitis E Virus of Subtype 3i in Chronically Infected Kidney Transplant Recipients in Southeastern France

Por Moal, Valérie, Gérolami, René, Ferretti, Audrey, Purgus, Raj, Devichi, Patricia, Burtey, Stéphane, Colson, Philippe
Publicado no J Clin Microbiol (2014)

Thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome

Por Sallée, Marion, Ismail, Khalil, Fakhouri, Fadi, Vacher-Coponat, Henri, Moussi-Francés, Julie, Frémaux-Bacchi, Véronique, Burtey, Stéphane
Publicado em 2013

Vancomycin-induced Henoch-Schönlein purpura: a case report

Por Bataille, Stanislas, Daumas, Aurélie, Tasei, Anne-Marie, Jourde-Chiche, Noémie, Dussol, Bertrand, Burtey, Stéphane, Taugourdeau, Solène, Berland, Yvon, Chiche, Laurent
Publicado em 2012

Acute tubulointerstitial nephritis complicating Legionnaires' disease: a case report

Por Daumas Aurélie, El-Mekaoui Fadwa, Bataille Stanislas, Daniel Laurent, Caporossi Jean-Marie, Fournier Pierre-Edouard, Burtey Stéphane, Dussol Bertrand, Berland Yvon, Jourde-Chiche Noémie
Publicado em 2012-04-01

Acute tubulointerstitial nephritis complicating Legionnaires' disease: a case report

Por Daumas, Aurélie, El-Mekaoui, Fadwa, Bataille, Stanislas, Daniel, Laurent, Caporossi, Jean-Marie, Fournier, Pierre-Edouard, Burtey, Stéphane, Dussol, Bertrand, Berland, Yvon, Jourde-Chiche, Noémie
Publicado em 2012

Trends in Survival and Renal Recovery in Patients with Multiple Myeloma or Light-Chain Amyloidosis on Chronic Dialysis

Por Decourt, Alexandre, Gondouin, Bertrand, Delaroziere, Jean Christophe, Brunet, Philippe, Sallée, Marion, Burtey, Stephane, Dussol, Bertrand, Ivanov, Vadim, Costello, Regis, Couchoud, Cecile, Jourde-Chiche, Noemie
Publicado no Clin J Am Soc Nephrol (2016)

The Cardiovascular Effect of the Uremic Solute Indole-3 Acetic Acid

Por Dou, Laetitia, Sallée, Marion, Cerini, Claire, Poitevin, Stéphane, Gondouin, Bertrand, Jourde-Chiche, Noemie, Fallague, Karim, Brunet, Philippe, Calaf, Raymond, Dussol, Bertrand, Mallet, Bernard, Dignat-George, Françoise, Burtey, Stephane
Publicado no J Am Soc Nephrol (2015)

Modular transcriptional repertoire analyses of adults with systemic lupus erythematosus reveal distinct type I and type II interferon signatures

Por Chiche, Laurent, Jourde-Chiche, Noémie, Whalen, Elizabeth, Presnell, Scott, Gersuk, Vivian, Dang, Kristen, Anguiano, Esperanza, Quinn, Charlie, Burtey, Stéphane, Berland, Yvon, Kaplanski, Gilles, Harle, Jean-Robert, Pascual, Virginia, Chaussabel, Damien
Publicado em 2014

Fractalkine Expression Induces Endothelial Progenitor Cell Lysis by Natural Killer Cells

Por Todorova, Dilyana, Sabatier, Florence, Doria, Evelyne, Lyonnet, Luc, Vacher Coponat, Henri, Robert, Stéphane, Despoix, Nicolas, Legris, Tristan, Moal, Valérie, Loundou, Anderson, Morange, Sophie, Berland, Yvon, George, Francoise Dignat, Burtey, Stéphane, Paul, Pascale
Publicado em 2011

Genetics and Outcome of Atypical Hemolytic Uremic Syndrome: A Nationwide French Series Comparing Children and Adults

Por Fremeaux-Bacchi, Véronique, Fakhouri, Fadi, Garnier, Arnaud, Bienaimé, Frank, Dragon-Durey, Marie-Agnès, Ngo, Stéphanie, Moulin, Bruno, Servais, Aude, Provot, François, Rostaing, Lionel, Burtey, Stéphane, Niaudet, Patrick, Deschênes, Georges, Lebranchu, Yvon, Zuber, Julien, Loirat, Chantal
Publicado em 2013

Epitope Spreading of Autoantibody Response to PLA2R Associates with Poor Prognosis in Membranous Nephropathy

Por Seitz-Polski, Barbara, Dolla, Guillaume, Payré, Christine, Girard, Christophe A., Polidori, Joel, Zorzi, Kevin, Birgy-Barelli, Eléonore, Jullien, Perrine, Courivaud, Cécile, Krummel, Thierry, Benzaken, Sylvia, Bernard, Ghislaine, Burtey, Stéphane, Mariat, Christophe, Esnault, Vincent L.M., Lambeau, Gérard
Publicado no J Am Soc Nephrol (2016)

Antibody-Dependent NK Cell Activation Is Associated with Late Kidney Allograft Dysfunction and the Complement-Independent Alloreactive Potential of Donor-Specific Antibodies

Por Legris, Tristan, Picard, Christophe, Todorova, Dilyana, Lyonnet, Luc, Laporte, Cathy, Dumoulin, Chloé, Nicolino-Brunet, Corinne, Daniel, Laurent, Loundou, Anderson, Morange, Sophie, Bataille, Stanislas, Vacher-Coponat, Henri, Moal, Valérie, Berland, Yvon, Dignat-George, Francoise, Burtey, Stéphane, Paul, Pascale
Publicado no Front Immunol (2016)

Membranous Nephropathy Associated With Immunological Disorder-Related Liver Disease: A Retrospective Study of 10 Cases

Por Dauvergne, Maxime, Moktefi, Anissa, Rabant, Marion, Vigneau, Cécile, Kofman, Tomek, Burtey, Stephane, Corpechot, Christophe, Stehlé, Thomas, Desvaux, Dominique, Rioux-Leclercq, Nathalie, Rouvier, Philippe, Knebelmann, Bertrand, Boffa, Jean-Jacques, Frouget, Thierry, Daugas, Eric, Jablonski, Mathieu, Dahan, Karine, Brocheriou, Isabelle, Remy, Philippe, Grimbert, Philippe, Lang, Philippe, Chazouilleres, Oliver, Sahali, Dil, Audard, Vincent
Publicado no Medicine (Baltimore) (2015)

Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans

Por Halbritter, Jan, Bizet, Albane A., Schmidts, Miriam, Porath, Jonathan D., Braun, Daniela A., Gee, Heon Yung, McInerney-Leo, Aideen M., Krug, Pauline, Filhol, Emilie, Davis, Erica E., Airik, Rannar, Czarnecki, Peter G., Lehman, Anna M., Trnka, Peter, Nitschké, Patrick, Bole-Feysot, Christine, Schueler, Markus, Knebelmann, Bertrand, Burtey, Stéphane, Szabó, Attila J., Tory, Kálmán, Leo, Paul J., Gardiner, Brooke, McKenzie, Fiona A., Zankl, Andreas, Brown, Matthew A., Hartley, Jane L., Maher, Eamonn R., Li, Chunmei, Leroux, Michel R., Scambler, Peter J., Zhan, Shing H., Jones, Steven J., Kayserili, Hülya, Tuysuz, Beyhan, Moorani, Khemchand N., Constantinescu, Alexandru, Krantz, Ian D., Kaplan, Bernard S., Shah, Jagesh V., Hurd, Toby W., Doherty, Dan, Katsanis, Nicholas, Duncan, Emma L., Otto, Edgar A., Beales, Philip L., Mitchison, Hannah M., Saunier, Sophie, Hildebrandt, Friedhelm
Publicado em 2013