Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kurt R Bessonen"'
Autor:
Rong He, Jonathan Chiou, Allison Chiou, Dong Chen, Constance P. Chen, Caroline Spethman, Kurt R. Bessonen, Jennifer L. Oliveira, Phuong L. Nguyen, Kaaren K. Reichard, James D. Hoyer, Simon D. Althoff, Dana J. Roh, Mechelle A. Miller, Ji Yuan, Horatiu Olteanu, Kebede Begna, Ayalew Tefferi, Hassan Alkhateeb, Mrinal M. Patnaik, Mark R. Litzow, Aref Al-Kali, David S. Viswanatha
Publikováno v:
Blood Cancer Journal, Vol 12, Iss 1, Pp 1-4 (2022)
Externí odkaz:
https://doaj.org/article/21ee0747a87649e5881a86cfab97180e
Autor:
Mrinal M. Patnaik, Rong He, David S. Viswanatha, Dragan Jevremovic, William J. Hogan, Zhuoer Xie, Hassan B. Alkhateeb, Aref Al-Kali, Naseema Gangat, Mohamad E. Salama, Ayalew Tefferi, Kurt R Bessonen, Mark R. Litzow, Mithun Vinod Shah, Ahmad Nanaa, Phuong L. Nguyen, Patricia T. Greipp, Animesh Pardanani
Publikováno v:
Blood Cancer Journal, Vol 11, Iss 6, Pp 1-4 (2021)
Blood Cancer Journal
Blood Cancer Journal
Autor:
Mechelle A Miller, Kaaren K. Reichard, Mark R. Litzow, Phuong L. Nguyen, James D. Hoyer, Elise R. Venable, Kurt R Bessonen, Constance P Chen, Aref Al-Kali, David S. Viswanatha, Dong Chen, Simon D Althoff, Jennifer L. Oliveira, Kebede H. Begna, Mrinal M. Patnaik, Rong He, Dana J Roh
Publikováno v:
American Journal of Clinical Pathology
Objectives SF3B1 mutations are the most common mutations in myelodysplastic syndromes (MDS). The International Working Group for the Prognosis of MDS (IWG-PM) recently proposed SF3B1-mutant MDS (SF3B1-mut-MDS) as a distinct disease subtype. We evalua