Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Dawn, Maze"'
Autor:
Maria Agustina Perusini, Claire Andrews, Eshetu G. Atenafu, Vikas Gupta, Dawn Maze, Andre C. Schuh, Karen WL. Yee, Aniket Bankar, Marta B. Davidson, Guillaume Richard-Carpentier, Steven M. Chan, Jad Sibai, Aaron D. Schimmer, Mark D. Minden, Hassan Sibai
Publikováno v:
Hematology, Vol 29, Iss 1 (2024)
ABSTRACTThis retrospective report presents the outcomes and adverse events (AEs) observed in 73 patients aged 60 years or older diagnosed with Philadelphia Chromosome-negative Acute Lymphoblastic Leukemia (Ph-negative ALL) treated with a pediatric-in
Externí odkaz:
https://doaj.org/article/860fe86b5d6c425b93b7c8cf45f165fa
Publikováno v:
eJHaem, Vol 4, Iss 1, Pp 241-245 (2023)
Abstract The impact of driver and other somatic mutations on pregnancy outcomes is unknown. The purpose of this study was to report the management and outcome of pregnancies in a cohort of myeloproliferative neoplasms (MPN) patients, particularly to
Externí odkaz:
https://doaj.org/article/b0a54877323749d4ab002a5cd48ded44
Autor:
Ibrahim Al Nabhani, Claire Andrews, Jad Sibai, Eshetu Atenafu, Taylor Young, Steven M. Chan, Vikas Gupta, Dawn Maze, Aaron D. Schimmer, Andre C. Schuh, Karen Yee, Hassan Sibai
Publikováno v:
eJHaem, Vol 4, Iss 1, Pp 232-235 (2023)
Abstract PEG‐asparaginase is used as a treatment for Philadelphia‐negative acute lymphoblastic leukemia. In pediatric studies, triglycerides (TGs) were affected more by PEG‐asparaginase than by native L‐asparaginase (10.0% vs. 5.5%). We condu
Externí odkaz:
https://doaj.org/article/e50e7e9e08b74513abd28ce4a7d9068c
Autor:
Maria Agustina Perusini, Vikas Gupta, Aniket Bankar, Jad Sibai, Mark Minden, Dawn Maze, Marta Davidson, Guillaume Richard-Carpentier, Steven M Chan, Andre Schuh, Karen Yee, Eshetu Atenafu, Hassan Sibai
Publikováno v:
HemaSphere, Vol 7, p e071333e (2023)
Externí odkaz:
https://doaj.org/article/03c405618e5249a5942832d5e65c32bd
Autor:
Aniket Bankar, Gopila Gupta, Verna Cheung, Jaime O. Claudio, Andrea Arruda, Hubert Tsui, Jose-Mario Capo-Chichi, Hassan Sibai, Marta Davidson, Dawn Maze, Vikas Gupta
Publikováno v:
HemaSphere, Vol 7, p e91985c2 (2023)
Externí odkaz:
https://doaj.org/article/64f74d5831c44f5c96bc5033fbbee5f1
Autor:
Tracy Murphy, Jinfeng Zou, Andrea Arruda, Ting Ting Wang, Zhen Zhao, Yangqiao Zheng, Vikas Gupta, Dawn Maze, Caroline McNamara, Mark D. Minden, Aaron Schimmer, Hassan Sibai, Karen Yee, Jose-Mario Capo-Chichi, Tracy Stockley, Andre Schuh, Scott V. Bratman, Steven M. Chan
Publikováno v:
Haematologica, Vol 109, Iss 2 (2023)
Externí odkaz:
https://doaj.org/article/163cd9b71d294983ad8ccc01a42dae00
Autor:
Anne Tierens, Elizabeth Kagotho, Satoru Shinriki, Andrew Seto, Adam C. Smith, Melanie Care, Dawn Maze, Hassan Sibai, Karen W. Yee, Andre C. Schuh, Dennis Dong Hwan Kim, Vikas Gupta, Mark D. Minden, Hirotaka Matsui, José-Mario Capo-Chichi
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
IntroductionInherited DDX41 mutations cause familial predisposition to hematologic malignancies including acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS), with the majority of DDX41 mutated MDS/AMLs described to date harboring germli
Externí odkaz:
https://doaj.org/article/ed7c8962d5984554ac1f4f6ebf6e56b8
Publikováno v:
eJHaem, Vol 3, Iss 2, Pp 526-532 (2022)
Externí odkaz:
https://doaj.org/article/da84a88bd6624e209ab072f5534688e3
Autor:
Ruiqi Chen, Xing Liu, Arjun D. Law, Solaf Kanfar, Dawn Maze, Steven M. Chan, Vikas Gupta, Karen W. Yee, Mark D. Minden, Aaron D. Schimmer, Andre C. Schuh, Caroline J. McNamara, Tracy Murphy, Anna Xu, Umberto Falcone, Jack Seki, Hassan Sibai
Publikováno v:
Current Oncology, Vol 28, Iss 1, Pp 128-137 (2020)
Background: venous thromboembolism (VTE) is a well-known complication in adults with acute lymphoblastic leukemia (ALL), especially in patients treated with asparaginase (ASNase)-including regiments. However, VTE risk in adult Philadelphia-positive A
Externí odkaz:
https://doaj.org/article/52f8617b934048549a4137619b3d7db4
Autor:
Dina Khalaf, Heather Bell, David Dale, Vikas Gupta, Hanna Faghfoury, Chantal F. Morel, Anne Tierens, David A. Weinstein, Jiong Yan, Santhosh Thyagu, Dawn Maze
Publikováno v:
JIMD Reports, Vol 49, Iss 1, Pp 37-42 (2019)
Abstract Congenital neutropenias due to mutations in ELANE, SBDS or HAX1 or in the setting of glycogen storage disease (GSD) which is caused by SLC37A4 mutation, often require prolonged granulocyte colony stimulating factor (G‐CSF) therapy to preve
Externí odkaz:
https://doaj.org/article/4c4cf88ce5244b0090ec15b121211297