Zobrazeno 11 - 14
of 14
pro vyhledávání: '"Sunil Babu"'
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:
James Essell, Roger M. Lyons, Elias J. Jabbour, Ralph V. Boccia, Guillermo Garcia-Manero, Mikkael A. Sekeres, Rami S. Komrokji, Yasmin Abaza, Richard G. Ghalie, Brian Heller, Gail J. Roboz, Philip Kuriakose, Farhad Ravandi, Hagop M. Kantarjian, David Wright, Bertrand Anz, Sunil Babu, Guillermo Montalban-Bravo, Jesus G. Berdeja, Michael B. Maris, James A. Reeves, Amy E. DeZern
BACKGROUND The prognosis of patients with higher risk myelodysplastic syndromes (MDS) remains poor despite available therapies. Histone deacetylase inhibitors have demonstrated activity in patients with MDS and in vitro synergy with azacitidine. METH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e6356e38d0b01f064458ed887e76fd3
https://europepmc.org/articles/PMC5432122/
https://europepmc.org/articles/PMC5432122/
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
Autor:
Kiran Yalamanchili, Rishi Sukhija, William H. Frishman, Wilbert S. Aronow, Sunil Babu, Ravi Kilaru, Stephen J. Peterson
Publikováno v:
Cardiology in review. 14(2)
We investigated the severity of coronary artery disease (CAD) diagnosed by coronary angiography performed because of suspected CAD in 102 persons, mean age 68 years, with rheumatoid arthritis (RA) and in 102 age-matched and sex-matched persons. CAD w
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