Zobrazeno 1 - 10
of 400
pro vyhledávání: '"K. Reichard"'
Autor:
Ayalew Tefferi, Animesh Pardanani, Kebede H. Begna, Aref Al-Kali, William J. Hogan, Mark R. Litzow, Rhett P. Ketterling, Kaaren K. Reichard, Naseema Gangat
Publikováno v:
Blood Cancer Journal, Vol 14, Iss 1, Pp 1-4 (2024)
Externí odkaz:
https://doaj.org/article/f92ca6110c604f30a18b2d513517e4cc
Autor:
Maymona G. Abdelmagid, Aref Al-Kali, Mark R. Litzow, Kebede H. Begna, William J. Hogan, Mirinal S. Patnaik, Shahrukh K. Hashmi, Michelle A. Elliott, Hassan Alkhateeb, Omer S. Karrar, Farah Fleti, Mohammed H. Elnayir, Candido E. Rivera, Hemant S. Murthy, James M. Foran, Mohamed A. Kharfan-Dabaja, Talha Badar, David S. Viswanatha, Kaaren K. Reichard, Naseema Gangat, Ayalew Tefferi
Publikováno v:
Blood Cancer Journal, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract We surveyed the performance of ponatinib, as salvage therapy, in a real-world setting of chronic phase chronic myeloid leukemia (CML-CP). Among 55 consecutive patients (median age 49 years) with relapsed/refractory CML-CP, 35 (64%) had faile
Externí odkaz:
https://doaj.org/article/5713a85908654b83ae61bd72a1efa7e7
Autor:
Maymona G. Abdelmagid, Aref Al-Kali, Kebede H. Begna, William J. Hogan, Mark R. Litzow, Farah Fleti, Abhishek A. Mangaonkar, Mrinal S. Patnaik, Michelle A. Elliott, Hassan Alkhateeb, Min Shi, Matthew T. Howard, Kaaren K. Reichard, Rhett P. Ketterling, Mithun Shah, Animesh Pardanani, Naseema Gangat, Ayalew Tefferi
Publikováno v:
Haematologica, Vol 108, Iss 9 (2023)
Externí odkaz:
https://doaj.org/article/b5f63e2f18184484ac81b5b1f81858e1
Autor:
Abhishek A. Mangaonkar, Terra L. Lasho, Christy Finke, Rhett P. Ketterling, Kaaren K. Reichard, Kristen McCullough, Naseema Gangat, Aref Al-Kali, Kebede H. Begna, William H. Hogan, Mark R. Litzow, Hassan Alkhateeb, Mithun Shah, Animesh Pardanani, Ayalew Tefferi, Najla H. Al Ali, Chetasi Talati, David Sallman, Eric Padron, Rami Komrokji, Mrinal M. Patnaik
Publikováno v:
Haematologica, Vol 107, Iss 5 (2022)
Externí odkaz:
https://doaj.org/article/058bd801e0344842925958441b67cbc2
Autor:
Alexander S Hines, Matthew J Koster, Allison R Bock, Ronald S Go, Kenneth J Warrington, Horatiu Olteanu, Terra L Lasho, Mrinal M Patnaik, Kaaren K Reichard
Publikováno v:
Rheumatology.
Objective To retrospectively identify patients with VEXAS syndrome (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome) among male patients with bone marrow vacuolization using a clinically applicable, targeted-screening approach. Meth
Autor:
Matthew J. Koster, Umar Ghaffar, Tanaz A. Kermani, Mrinal M. Patnaik, Ronald S. Go, Abhishek A. Mangaonkar, Kaaren K. Reichard, Horatiu Olteanu, Kenneth J. Warrington
Publikováno v:
Arthritis & Rheumatology.
Autor:
Fernanda Gutierrez-Rodrigues, Yael Kusne, Jenna Fernandez, Terra L Lasho, Ruba N Shalhoub, Xiaoyang Ma, Hugh Alessi, Christy M. Finke, Matthew J. Koster, Abhishek A. Mangaonkar, Kenneth J Warrington, Kebede Begna, Zhuoer Xie, Amanda K Ombrello, David S Viswanatha, Marcela A. Ferrada, Lorena Wilson, Ronald S. Go, Taxiarchis V. Kourelis, Kaaren K Reichard, Horatiu Olteanu, Ivana Darden, Dalton Hironaka, Lemlem Alemu, Sachiko Kajigaya, Rodrigo T. Calado, Emma M. Groarke, Sofia Rosenzweig, Daniel L Kastner, Katherine R Calvo, Colin O. Wu, Peter C. Grayson, Neal S Young, David B. Beck, Bhavisha A. Patel, Mrinal M. Patnaik
Publikováno v:
Blood Journal.
VEXAS is caused by somatic mutations in UBA1 (UBA1mut) and characterized by heterogenous systemic auto-inflammation and progressive hematologic manifestations, meeting criteria for myelodysplastic syndrome (MDS) and plasma cell dyscrasias. The landsc
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Autor:
Marie‐France Gagnon, Holly E. Berg, Reid G. Meyer, William R. Sukov, Daniel L. Van Dyke, Robert B. Jenkins, Patricia T. Greipp, Erik C. Thorland, Nicole L. Hoppman, Xinjie Xu, Linda B. Baughn, Kaaren K. Reichard, Rhett P. Ketterling, Jess F. Peterson
Publikováno v:
Genes, Chromosomes and Cancer. 61:629-634
Autor:
Mark J. Routbort, Guillermo Garcia-Manero, Kyle Devins, Paola Dal Cin, Kim Anh Do, Rashmi Kanagal-Shamanna, Olga Pozdnyakova, Sa A. Wang, Patricia T. Greipp, Robert P. Hasserjian, Tracy I. George, Kaaren K. Reichard, Keyur P. Patel, Eric D. Hsi, Adam Bagg, Attilio Orazi, L. Jeffrey Medeiros, Srdan Verstovsek, Heesun J. Rogers, Daniel A. Arber, Carlos E. Bueso-Ramos, Faezeh Darbaniyan, Julia T. Geyer
Publikováno v:
Modern Pathology. 35:470-479
Classification of myeloid neoplasms with isolated isochromosome i(17q) [17p deletion with inherent monoallelic TP53 loss plus 17q duplication] is controversial. Most cases fall within the WHO unclassifiable myelodysplastic/myeloproliferative neoplasm