Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Siobán B, Keel"'
Publikováno v:
Blood Advances, Vol 3, Iss 16, Pp 2470-2473 (2019)
Externí odkaz:
https://doaj.org/article/e3508e80d37f47a691c5b2728fb76de2
Autor:
Anna B. Halpern, Megan Othus, Genevieve Alcorn, Zahra Ali, Kelsey-Leigh A. Garcia, Mary-Elizabeth M. Percival, Siobán B. Keel, Ryan D. Cassaday, Pamela S. Becker, Elihu H. Estey, Roland B. Walter
Publikováno v:
Leukemia. 36:1386-1389
Autor:
Kelsey‐Leigh A. Garcia, Sindhu Cherian, Philip A. Stevenson, Christen H. Martino, Andrei R. Shustov, Pamela S. Becker, Mary‐Elizabeth M. Percival, Vivian G. Oehler, Anna B. Halpern, Roland B. Walter, Johnnie J. Orozco, Siobán B. Keel, Elihu H. Estey, Ryan D. Cassaday
Publikováno v:
Cancer. 128:1411-1417
Potential involvement of the central nervous system (CNS) by acute lymphoblastic leukemia is typically evaluated by a conventional cytospin (CC) of cerebrospinal fluid (CSF). Multiparameter flow cytometry (MFC) is generally more sensitive and specifi
Autor:
Amy K. Dickey, Hetanshi Naik, Siobán B. Keel, Cynthia Levy, Simon W. Beaven, Sarina B. Elmariah, Angelika L. Erwin, Robert J. Goddu, Karli Hedstrom, Rebecca K. Leaf, Mohamed Kazamel, Marshall Mazepa, Lisa Liang Philpotts, John Quigley, Haya Raef, Sean R. Rudnick, Behnam Saberi, Manish Thapar, Jonathan Ungar, Bruce Wang, Manisha Balwani
Publikováno v:
Journal of the American Academy of Dermatology.
Erythropoietic protoporphyria and X-linked protoporphyria are rare genetic photodermatoses. Limited expertise with these disorders among physicians leads to diagnostic delays. Here, we present evidence-based consensus guidelines for the diagnosis, mo
Autor:
Siobán B. Keel, Angela Scott, Marilyn Sanchez-Bonilla, Phoenix A. Ho, Suleyman Gulsuner, Colin C. Pritchard, Janis L. Abkowitz, Mary-Claire King, Tom Walsh, Akiko Shimamura
Publikováno v:
Haematologica, Vol 101, Iss 11 (2016)
The clinical and histopathological distinctions between inherited versus acquired bone marrow failure and myelodysplastic syndromes are challenging. The identification of inherited bone marrow failure/myelodysplastic syndromes is critical to inform a
Externí odkaz:
https://doaj.org/article/ea5a2319576b4257aa6cc5cd2f67a45b
Autor:
Anna B, Halpern, Megan, Othus, Genevieve, Alcorn, Zahra, Ali, Kelsey-Leigh A, Garcia, Mary-Elizabeth M, Percival, Siobán B, Keel, Ryan D, Cassaday, Pamela S, Becker, Elihu H, Estey, Roland B, Walter
Publikováno v:
Leukemia. 36(5)
Autor:
Michael Y. Zhang, Siobán B. Keel, Tom Walsh, Ming K. Lee, Suleyman Gulsuner, Amanda C. Watts, Colin C. Pritchard, Stephen J. Salipante, Michael R. Jeng, Inga Hofmann, David A. Williams, Mark D. Fleming, Janis L. Abkowitz, Mary-Claire King, Akiko Shimamura
Publikováno v:
Haematologica, Vol 100, Iss 1 (2015)
Accurate and timely diagnosis of inherited bone marrow failure and inherited myelodysplastic syndromes is essential to guide clinical management. Distinguishing inherited from acquired bone marrow failure/myelodysplastic syndrome poses a significant
Externí odkaz:
https://doaj.org/article/99cc2267d23347f9a4d88322df9476dd
Autor:
Andreea Reilly, J. Philip Creamer, Sintra Stewart, Massiel C. Stolla, Yuchuan Wang, Jing Du, Rachel Wellington, Stephanie Busch, Elihu H. Estey, Pamela S. Becker, Min Fang, Siobán B. Keel, Janis L. Abkowitz, Lorinda A. Soma, Jian Ma, Zhijun Duan, Sergei Doulatov
Publikováno v:
Cell Stem Cell
Abnormal nuclear morphology is a hallmark of malignant cells widely used in cancer diagnosis. Pelger-Huët anomaly (PHA) is a common abnormality of neutrophil nuclear morphology of unknown molecular etiology in myeloid neoplasms (MNs). We show that l
Autor:
Anna B, Halpern, Nicholas P, Howard, Megan, Othus, Paul C, Hendrie, Nikita V, Baclig, Sarah A, Buckley, Mary-Elizabeth M, Percival, Pamela S, Becker, Bart L, Scott, Vivian G, Oehler, Terry B, Gernsheimer, Siobán B, Keel, Johnnie J, Orozco, Ryan D, Cassaday, Andrei R, Shustov, Garrett A, Hartley, Verna L, Welch, Elihu H, Estey, Roland B, Walter
Publikováno v:
Leukemia. 34(2)
Autor:
Ashutosh, Lal, Trisha E, Wong, Jennifer, Andrews, Vinod V, Balasa, Jong H, Chung, Craig M, Forester, Alan K, Ikeda, Siobán B, Keel, Monica B, Pagano, Geetha, Puthenveetil, Sanjay J, Shah, Jennifer C, Yu, Elliott P, Vichinsky
Publikováno v:
Transfusion. 58(12)
The severe forms of thalassemia are the most common inherited anemias managed with regular blood transfusion therapy. Transfusion policies and complications are critical to quality of life and survival, but there is a lack of standardized care.A surv