Zobrazeno 1 - 10
of 150
pro vyhledávání: '"Phuong L. Nguyen"'
Publikováno v:
Blood Cancer Journal, Vol 12, Iss 1, Pp 1-5 (2022)
Externí odkaz:
https://doaj.org/article/a6babd2d2ab94bbeac0893e2812cdd2b
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:
Mazen Osman, Zeynettin Akkus, Dragan Jevremovic, Phuong L. Nguyen, Dana Roh, Aref Al-Kali, Mrinal M. Patnaik, Ahmad Nanaa, Samia Rizk, Mohamed E. Salama
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 11, p 2264 (2021)
The accurate diagnosis of chronic myelomonocytic leukemia (CMML) and acute myeloid leukemia (AML) subtypes with monocytic differentiation relies on the proper identification and quantitation of blast cells and blast-equivalent cells, including promon
Externí odkaz:
https://doaj.org/article/cd8e3b783392404f96c82fc9658892cf
Publikováno v:
Emerging Infectious Diseases, Vol 9, Iss 1, Pp 135-137 (2003)
Externí odkaz:
https://doaj.org/article/f78e36b282fc4ef2866bf540d5465aa1
Autor:
Jennifer L Oliveira, Christineil H Thompson, Siva Arumugam Saravanaperumal, Tejaswi Koganti, Garrett Jenkinson, Molly S Hein, Mira A Kohorst, Linda Hasadsri, Phuong L Nguyen, Dietrich Matern, Benjamin R Kipp, Eric W Klee, Eric D Wieben, James D Hoyer, Aruna Rangan
Publikováno v:
Clinical Chemistry.
Background Large β-globin gene cluster deletions (hereditary persistence of fetal hemoglobin [Hb] or β-, δβ-, γδβ-, and ϵγδβ-thalassemia), are associated with widely disparate phenotypes, including variable degrees of microcytic anemia and
Autor:
Ahmad Nanaa, Ayalew Tefferi, Dragan Jevremovic, Aref Al-Kali, Abhishek A. Mangaonkar, Naseema Gangat, Mark R. Litzow, Mrinal M. Patnaik, Hassan B. Alkhateeb, Patricia T. Greipp, Lisa Sproat, Mohamad E. Salama, Mithun Vinod Shah, Rong He, Talha Badar, David S. Viswanatha, Phuong L. Nguyen, James M. Foran
Publikováno v:
Blood Advances
Key Points Isolated and comutated DDX41 myeloid neoplasms have different characteristics.DDX41-mutated AML has a relatively favorable outcome comparable to core binding factor AML.
Visual Abstract
DDX41 mutations (germline and somatic) are
Visual Abstract
DDX41 mutations (germline and somatic) are
Autor:
Mina Samir Erian Hanna, Aminah Jatoi, Nichole A. Martin, Samantha Mannion, Yahya Almodallal, Phuong L. Nguyen, Kathryn D. Cook
Publikováno v:
Journal of Geriatric Oncology. 12:1220-1224
Background Metastatic cancer in nonagenarians and those older is rare and understudied. Here we explored whether these patients appear to benefit from antineoplastic therapy and whether outcomes differ based on whether or not untreated patients had a
Autor:
Scott M. Stanley, Aleja Parsons, Howard J. Markman, Phuong L. Nguyen, Kayla Knopp, Shelby B. Scott
Publikováno v:
Family Process. 60:1249-1263
A large body of existing research on African American relationships perpetuates a deficit model that assumes Eurocentric norms and emphasizes between-group differences (e.g., cross-racial comparisons with the majority group-European Americans). The c
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