Zobrazeno 1 - 10
of 681
pro vyhledávání: '"Pierre, Ronco"'
Autor:
Alexandra Barry, Michelle T. McNulty, Xiaoyuan Jia, Yask Gupta, Hanna Debiec, Yang Luo, China Nagano, Tomoko Horinouchi, Seulgi Jung, Manuela Colucci, Dina F. Ahram, Adele Mitrotti, Aditi Sinha, Nynke Teeninga, Gina Jin, Shirlee Shril, Gianluca Caridi, Monica Bodria, Tze Y. Lim, Rik Westland, Francesca Zanoni, Maddalena Marasa, Daniel Turudic, Mario Giordano, Loreto Gesualdo, Riccardo Magistroni, Isabella Pisani, Enrico Fiaccadori, Jana Reiterova, Silvio Maringhini, William Morello, Giovanni Montini, Patricia L. Weng, Francesco Scolari, Marijan Saraga, Velibor Tasic, Domenica Santoro, Joanna A. E. van Wijk, Danko Milošević, Yosuke Kawai, Krzysztof Kiryluk, Martin R. Pollak, Ali Gharavi, Fangmin Lin, Ana Cristina Simœs e Silva, Ruth J. F. Loos, Eimear E. Kenny, Michiel F. Schreuder, Aleksandra Zurowska, Claire Dossier, Gema Ariceta, Magdalena Drozynska-Duklas, Julien Hogan, Augustina Jankauskiene, Friedhelm Hildebrandt, Larisa Prikhodina, Kyuyoung Song, Arvind Bagga, Hae Cheong, Gian Marco Ghiggeri, Prayong Vachvanichsanong, Kandai Nozu, Dongwon Lee, Marina Vivarelli, Soumya Raychaudhuri, Katsushi Tokunaga, Simone Sanna-Cherchi, Pierre Ronco, Kazumoto Iijima, Matthew G. Sampson
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-13 (2023)
Abstract Pediatric steroid-sensitive nephrotic syndrome (pSSNS) is the most common childhood glomerular disease. Previous genome-wide association studies (GWAS) identified a risk locus in the HLA Class II region and three additional independent risk
Externí odkaz:
https://doaj.org/article/1df6c689ebb545a68dd4d7a57a5fefc6
Autor:
Frank Bienaimé, Mordi Muorah, Marie Metzger, Melanie Broeuilh, Pascal Houiller, Martin Flamant, Jean-Philippe Haymann, Jacky Vonderscher, Jacques Mizrahi, Gérard Friedlander, Bénédicte Stengel, Fabiola Terzi, François Vrtovsnik, Eric Daugas, Emmanuelle Vidal-Petiot, Christian Jacquot, Alexandre Karras, Stéphane Roueff, Eric Thervet, Pascal Houillier, Marie Courbebaisse, Dominique Eladari et Gérard Maruani, Pablo Urena-Torres, Jean-Jacques Boffa, Pierre Ronco, H. Fessi, Eric Rondeau, Emmanuel Letavernier, Nahid Tabibzadeh
Publikováno v:
EBioMedicine, Vol 93, Iss , Pp 104635- (2023)
Summary: Background: Urinary biomarkers may improve the prediction of chronic kidney disease (CKD) progression. Yet, data reporting the applicability of most commercial biomarker assays to the detection of their target analyte in urine together with
Externí odkaz:
https://doaj.org/article/7817ac03d9a2498697a600d278abdb45
Autor:
Emmanuel Estève, David Buob, Frédéric Jamme, Chantal Jouanneau, Slavka Kascakova, Jean-Philippe Haymann, Emmanuel Letavernier, Louise Galmiche, Pierre Ronco, Michel Daudon, Dominique Bazin, Matthieu Réfrégiers
Publikováno v:
Journal of Synchrotron Radiation, Vol 29, Iss 1, Pp 214-223 (2022)
Renal oxalosis is a rare cause of renal failure whose diagnosis can be challenging. Synchrotron deep ultraviolet (UV) fluorescence was assayed to improve oxalosis detection on kidney biopsies spatial resolution and sensitivity compared with the Fouri
Externí odkaz:
https://doaj.org/article/dce272ea25564f1cbb15fe3d3da852f1
Autor:
Edmund Y. M. Chung, MD, Katrina Blazek, BMedSci, Armando Teixeira-Pinto, PhD, Ankit Sharma, PhD, Siah Kim, PhD, Yingxin Lin, PhD, Karen Keung, PhD, Bhadran Bose, MBBS, Lukas Kairaitis, PhD, Hugh McCarthy, PhD, Pierre Ronco, PhD, Stephen I. Alexander, MD, Germaine Wong, PhD
Publikováno v:
Transplantation Direct, Vol 8, Iss 9, p e1357 (2022)
Background. Recurrent membranous nephropathy (MN) posttransplantation affects 35% to 50% of kidney transplant recipients (KTRs) and accounts for 50% allograft loss 5 y after diagnosis. Predictive factors for recurrent MN may include HLA-D risk allele
Externí odkaz:
https://doaj.org/article/be8d4697ae2c4af78ad7b0e22122bbcc
Autor:
Pierre-Emmanuel Cailleaux, Agnes Ostertag, Marie Metzger, Bénédicte Stengel, Julie Boucquemont, Pascal Houillier, Martin Flamant, Pablo Ureña-Torres, Martine Cohen-Solal, Emmanuel Letavernier, Pierre Ronco, Hafedh Fessi, Eric Daugas, Caroline du Halgouet, Renaud de La Faille, Christian d’Auzac, Gerard Maruani, Marion Vallet, Cédric Gauci, Jean Philippe Haymann, Eric Thervet, Jean-Jacques Boffa, François Vrtovsnik, Marc Froissart, Laurence Nicolet-Barousse, Mélanie Roland, Christian Jacquot
Publikováno v:
Kidney International Reports, Vol 6, Iss 6, Pp 1525-1536 (2021)
Introduction: Chronic kidney disease (CKD) exposes to an increased incidence of fragility fractures. International guidelines recommend performing bone mineral density (BMD) if the results will impact treatment decisions. It remains unknown where bon
Externí odkaz:
https://doaj.org/article/6a3665bae07e47ecbe65cd0403608b8b
Autor:
Bingileki F Lwezaula, Oluwatoyin I Ameh, Udeme E Ekrikpo, Francois CJ Botha, Ugochi S Okpechi-Samuel, Nicola Wearne, Pierre Ronco, Aminu K Bello, Ikechi G. Okpechi
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-8 (2021)
Abstract Background: Serum and tissue-based tests using phospholipase A2 receptor 1 (PLA2R) and thrombospondin type-1 domain containing 7A (THSD7A) are established immune biomarkers for the diagnosis of primary membranous nephropathy (PMN). This stud
Externí odkaz:
https://doaj.org/article/41a87cfa91a64dc4b964a250e88d6db6
Autor:
Aishwarya Ravindran, Benjamin Madden, M. Cristine Charlesworth, Rishi Sharma, Amit Sethi, Hanna Debiec, Daniel Cattran, Fernando C. Fervenza, Richard J. Smith, Pierre Ronco, Sanjeev Sethi
Publikováno v:
Kidney International Reports, Vol 5, Iss 5, Pp 618-626 (2020)
Introduction: Membranous nephropathy (MN) is the most common cause of nephrotic syndrome in Caucasian adults. Phospholipase A2 receptor (PLA2R)– and exostosin 1 (EXT1)/exostosin 2 (EXT2)–associated MN represent the most common primary and seconda
Externí odkaz:
https://doaj.org/article/c2556a86e4e04b438df4b3d80f2b158f
Autor:
Jingyuan Xie, Lili Liu, Nikol Mladkova, Yifu Li, Hong Ren, Weiming Wang, Zhao Cui, Li Lin, Xiaofan Hu, Xialian Yu, Jing Xu, Gang Liu, Yasar Caliskan, Carlo Sidore, Olivia Balderes, Raphael J. Rosen, Monica Bodria, Francesca Zanoni, Jun Y. Zhang, Priya Krithivasan, Karla Mehl, Maddalena Marasa, Atlas Khan, Fatih Ozay, Pietro A. Canetta, Andrew S. Bomback, Gerald B. Appel, Simone Sanna-Cherchi, Matthew G. Sampson, Laura H. Mariani, Agnieszka Perkowska-Ptasinska, Magdalena Durlik, Krzysztof Mucha, Barbara Moszczuk, Bartosz Foroncewicz, Leszek Pączek, Ireneusz Habura, Elisabet Ars, Jose Ballarin, Laila-Yasmin Mani, Bruno Vogt, Savas Ozturk, Abdülmecit Yildiz, Nurhan Seyahi, Hakki Arikan, Mehmet Koc, Taner Basturk, Gonca Karahan, Sebahat Usta Akgul, Mehmet Sukru Sever, Dan Zhang, Domenico Santoro, Mario Bonomini, Francesco Londrino, Loreto Gesualdo, Jana Reiterova, Vladimir Tesar, Claudia Izzi, Silvana Savoldi, Donatella Spotti, Carmelita Marcantoni, Piergiorgio Messa, Marco Galliani, Dario Roccatello, Simona Granata, Gianluigi Zaza, Francesca Lugani, GianMarco Ghiggeri, Isabella Pisani, Landino Allegri, Ben Sprangers, Jin-Ho Park, BeLong Cho, Yon Su Kim, Dong Ki Kim, Hitoshi Suzuki, Antonio Amoroso, Daniel C. Cattran, Fernando C. Fervenza, Antonello Pani, Patrick Hamilton, Shelly Harris, Sanjana Gupta, Chris Cheshire, Stephanie Dufek, Naomi Issler, Ruth J. Pepper, John Connolly, Stephen Powis, Detlef Bockenhauer, Horia C. Stanescu, Neil Ashman, Ruth J. F. Loos, Eimear E. Kenny, Matthias Wuttke, Kai-Uwe Eckardt, Anna Köttgen, Julia M. Hofstra, Marieke J. H. Coenen, Lambertus A. Kiemeney, Shreeram Akilesh, Matthias Kretzler, Lawrence H. Beck, Benedicte Stengel, Hanna Debiec, Pierre Ronco, Jack F. M. Wetzels, Magdalena Zoledziewska, Francesco Cucca, Iuliana Ionita-Laza, Hajeong Lee, Elion Hoxha, Rolf A. K. Stahl, Paul Brenchley, Francesco Scolari, Ming-hui Zhao, Ali G. Gharavi, Robert Kleta, Nan Chen, Krzysztof Kiryluk
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-18 (2020)
Membranous nephropathy (MN) is a rare autoimmune disease of podocyte-directed antibodies, such as anti-phospholipase A2 receptor. Here, the authors report a genome-wide association study for MN and identify two previously unreported loci encompassing
Externí odkaz:
https://doaj.org/article/673c37d7cf9b414b91486e389bd81da8
Autor:
Nicolas Hanset, Emmanuel Esteve, Emmanuelle Plaisier, Catherine Johanet, Pierre-Antoine Michel, Jean-Jacques Boffa, Patrick Fievet, Laurent Mesnard, Johann Morelle, Pierre Ronco, Karine Dahan
Publikováno v:
Kidney International Reports, Vol 5, Iss 3, Pp 331-338 (2020)
Introduction: Patients with phospholipase A2 receptor (PLA2R)–associated membranous nephropathy and stage 4 or 5 chronic kidney disease are at high risk of end-stage kidney disease. In recent years, rituximab (RTX) emerged as a safe and efficient t
Externí odkaz:
https://doaj.org/article/1048bd80817a420b88f96ae03a3447fa
Autor:
Cornelia Dähnrich, Sandra Saschenbrecker, Iva Gunnarsson, Wolfgang Schlumberger, Pierre Ronco, Hanna Debiec
Publikováno v:
Kidney International Reports, Vol 5, Iss 2, Pp 182-188 (2020)
Introduction: Autoantibodies against the M-type phospholipase A2 receptor (PLA2R) are important markers in the diagnosis and monitoring of primary membranous nephropathy (pMN). For the detection of anti-PLA2R autoantibodies, a standardized recombinan
Externí odkaz:
https://doaj.org/article/2129c9949720448ab8dadca5e6056f55