Zobrazeno 1 - 10
of 13
pro vyhledávání: '"David Philibert"'
Autor:
Nidal El Yamani, Gabrielle Cote, Julie Riopel, Nicolas Marcoux, Fabrice Mac-Way, David Philibert, Mohsen Agharazii
Publikováno v:
Kidney Medicine, Vol 5, Iss 8, Pp 100682- (2023)
Immune checkpoint inhibitors are known to have a wide range of autoimmune toxicities, such as acute interstitial nephritis. Immunotherapy induced glomerulonephritis has been described, but anti-glomerular basement membrane disease (anti-GBM) is rarel
Externí odkaz:
https://doaj.org/article/0467b9763f55404e94c8ae21c2b292a1
Autor:
Anne-Laure Lapeyraque, Martin Bitzan, Imad Al-Dakkak, Mira Francis, Shih-Han S. Huang, Roger Kaprielian, Loree Larratt, Katerina Pavenski, Christine Ribic, Axel Tosikyan, Christoph Licht, David Philibert
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 7 (2020)
Background: Atypical hemolytic uremic syndrome (aHUS) is an extremely rare, heterogeneous disease of uncontrolled activation of the alternative complement pathway that is difficult to diagnose. We have evaluated the Canadian patients enrolled in the
Externí odkaz:
https://doaj.org/article/f5abb0f45f7045dab2ce21463229fe09
Autor:
Ellen T. McCarthy, Brad H. Rovin, Sanjeev Sethi, James F. Simon, Patrick E. Gipson, Sean J. Barbour, Paul Brenchley, Lee A. Hebert, John R. Sedor, Fernando C. Fervenza, Jonathan Ashley Jefferson, Nelson Leung, Tingting Li, Michelle Hladunewich, Daniel C Cattran, Lada Beara-Lasic, Pietro A. Canetta, Heather Beanlands, Carmen Avila-Casado, Amy N. Sussman, Stephen B. Erickson, Bruno R. da Costa, Dana V. Rizk, Jay Radhakrishnan, Heather N. Reich, Richard A. Lafayette, Dolly F. Green, Gerald B. Appel, David Philibert, Luis A. Juncos, Nabeel Aslam, Samir V. Parikh, Dominic K. Lee, Lesley F. Thomas, Samuel S. Blumenthal, Debbie S. Gipson, John C. Lieske, Peter Jüni
Publikováno v:
MENTOR Investigators 2019, ' Rituximab or Cyclosporine in the Treatment of Membranous Nephropathy ', The New England Journal of Medicine, vol. 381, no. 1, pp. 36-46 . https://doi.org/10.1056/NEJMoa1814427
BACKGROUND: B-cell anomalies play a role in the pathogenesis of membranous nephropathy. B-cell depletion with rituximab may therefore be noninferior to treatment with cyclosporine for inducing and maintaining a complete or partial remission of protei
Autor:
Katerina Pavenski, Axel Tosikyan, Shih-Han S. Huang, David Philibert, Martin Bitzan, Loree Larratt, Christine Ribic, Mira Francis, Christoph Licht, Anne-Laure Lapeyraque, Imad Al-Dakkak, Roger Kaprielian
Publikováno v:
Canadian Journal of Kidney Health and Disease
Canadian Journal of Kidney Health and Disease, Vol 7 (2020)
Canadian Journal of Kidney Health and Disease, Vol 7 (2020)
Atypical hemolytic uremic syndrome (aHUS) is an extremely rare, heterogeneous disease of uncontrolled activation of the alternative complement pathway that is difficult to diagnose. We have evaluated the Canadian patients enrolled in the Global aHUS
Publikováno v:
Nephrology Dialysis Transplantation. 23:359-363
Background. Haematopoietic stem cell transplantation (HSCT) has gained worldwide acceptance as a therapeutic option for many haematological and non-haematological conditions. Local experience supports that electrolyte abnormalities are quite common;
Autor:
Daniel C. Cattran, David Philibert
Publikováno v:
Core Concepts in Parenchymal Kidney Disease ISBN: 9781461481652
Glomerular diseases have a wide spectrum of presentation from microscopic hematuria, asymptomatic proteinuria, and nephrotic syndrome to rapidly progressive renal failure. Each of these clinical scenarios warrants a specific diagnostic approach aimed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44fcc4079b6616ca597a83fe5327ea80
https://doi.org/10.1007/978-1-4614-8166-9_1
https://doi.org/10.1007/978-1-4614-8166-9_1
Autor:
Sacha A. De Serres, Eva Latulippe, Isabelle Houde, Mathieu Rousseau-Gagnon, David Philibert, Julie Riopel, Michael McRae
Publikováno v:
Rheumatology. 53:1151-1152
Autor:
Daniel C. Cattran, David Philibert
Publikováno v:
Nature clinical practice. Nephrology. 4(10)
Membranous nephropathy, focal segmental glomerulosclerosis and IgA nephropathy are the most commonly recognized types of primary glomerulonephritis that progress to end-stage renal disease. Persistent proteinuria is a major determinant of such progre
Publikováno v:
Seminars in nephrology. 28(1)
IgA nephropathy is the most common biopsy-proven pattern of glomerulonephritis in the world. Many factors, both clinical and histologic, have been suggested to impact on prognosis. We review the wide variations in how patients with immunoglobulin A n
Publikováno v:
Nephrology Dialysis Transplantation. 21:1134-1135