Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sunil Babu"'
Autor:
Ang Li, Jason C. Chandler, Davey B. Daniel, Félix Couture, Sunil Babu, Vijay Gunuganti, Maen A. Hussein, Robert M. Jotte, Samer Kasbari, Michael McCleod, Edward B. Garon, Justin N. Baker, Nivedita Aanur, Lawrence H. Einhorn, Leora Horn, Ben C. Creelan, Petros Nikolinakos, George P. Keogh, David R. Spigel, Craig Reynolds, Natasha B. Leighl, David M. Waterhouse, George R. Blumenschein
Publikováno v:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 38(33)
PURPOSE Limited data exist on the optimal duration of immunotherapy, including for non–small-cell lung cancer (NSCLC). We present an exploratory analysis of CheckMate 153, a largely community-based phase IIIb/IV study, to evaluate the impact of 1-y
Autor:
Petra Muus, David J. Cohen, Antonella Trivelli, Osama Gaber, Christoph Licht, Giuseppe Remuzzi, Sunil Babu, Camille L. Bedrosian, Maria Herthelius, Kenneth W. Douglas, Yahsou Delmas, Neil S. Sheerin, Chantal Loirat, Maryvonne Hourmant, Larry A. Greenbaum, Christophe Legendre, Timothy H.J. Goodship, Richard R. Furman
Publikováno v:
Kidney International. Supplement, 87, 5, pp. 1061-73
Kidney International. Supplement, 87, 1061-73
Kidney International. Supplement, 87, 1061-73
Contains fulltext : 155154.pdf (Publisher’s version ) (Open Access) Atypical hemolytic uremic syndrome (aHUS) is a rare, possibly life-threatening disease characterized by platelet activation, hemolysis and thrombotic microangiopathy (TMA) leading
Autor:
Richard R. Furman, Bruno Moulin, Timothy H.J. Goodship, Sunil Babu, Maria Herthelius, Jens Nürnberger, Neil S. Sheerin, Petra Muus, C. Bedrosian, Rebecca Sberro-Soussan, C. Bingham, Christoph Licht, Yvon Lebranchu, Jan Menne, Christophe Mariat, B. Severino, Frank Eitner, Y. Delmas, Osama Gaber, T. Richard, David J. Cohen, Thorsten Feldkamp, Denis Fouque, Kenneth W. Douglas, Diana Karpman, Chantal Loirat, Maryvonne Hourmant, Masayo Ogawa, Antonella Trivelli, Giuseppe Remuzzi, Ch. Legendre, L.B. Zimmerhackl, Laurence Greenbaum
Publikováno v:
The New England Journal of Medicine, 368, 23, pp. 2169-81
New England Journal of Medicine; 368(23), pp 2169-2181 (2013)
The New England Journal of Medicine, 368, 2169-81
New England Journal of Medicine; 368(23), pp 2169-2181 (2013)
The New England Journal of Medicine, 368, 2169-81
Item does not contain fulltext BACKGROUND: Atypical hemolytic-uremic syndrome is a genetic, life-threatening, chronic disease of complement-mediated thrombotic microangiopathy. Plasma exchange or infusion may transiently maintain normal levels of hem