Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ashley Galvin"'
Autor:
Grzegorz Nalepa, Etan Orgel, Richard H. Ho, Matthew J. Oberley, Mark D. Fleming, Yves D. Pastore, Courtney D. DiNardo, Joseph Rosenthal, M. Tarek Elghetany, Akiko Shimamura, Maggie Malsch, Bradford Siegele, Ashley Galvin, Michelle Manalang, Elissa Furutani, Iftikhar Hanif, James A. Connelly, Jordan Henry Larson, Nicole Karras, Lauri Burroughs, Edie Weller, Farid Boulad, Kasiani C. Myers, Blanche P. Alter, Carlos E. Bueso-Ramos, Maxim Norkin, Valérie Arsenault, Taizo A. Nakano, Kelly Walkovich, Lisa J. McReynolds, Stella M. Davies, Paul Castillo
Publikováno v:
Lancet Haematol
Summary Background Data to inform surveillance and treatment for leukaemia predisposition syndromes are scarce and recommendations are largely based on expert opinion. This study aimed to investigate the clinical features and outcomes of patients wit
Autor:
John M. Gansner, James Bowman, Jane E. Churpek, Gwen M. Muscato, Richard H. Ho, Adam J. Lamble, Mark D. Fleming, Robert H. Klein, Alison A. Bertuch, Shanshan Liu, Wendy Stock, Jeffrey M. Lipton, Christian Brendel, Ashley Galvin, James A. Connelly, Nicholas D. Camarda, Christopher J. Gibson, Christopher D. Bahl, Chad E. Harris, Kasiani C. Myers, Sioban Keel, R. Coleman Lindsley, Kelly Walkovich, Maggie Malsch, Bonnie W Lau, Alyssa L. Kennedy, Kaitlyn Ballotti, John R. Edwards, David C. Dale, Akiko Shimamura, Stella M. Davies, Elliot Stieglitz, Scott L. Carter, Paul Castillo, Steffen Boettcher, Taizo A. Nakano, Adrianna Vlachos, Maxim Norkin, Elissa Furutani, Edie Weller, Nobuko Hijiya, Inga Hofmann, James N. Huang
Publikováno v:
Nature communications, vol 12, iss 1
Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
Nature Communications
To understand the mechanisms that mediate germline genetic leukemia predisposition, we studied the inherited ribosomopathy Shwachman-Diamond syndrome (SDS), a bone marrow failure disorder with high risk of myeloid malignancies at an early age. To def
Autor:
Joan Moore, Stella M. Davies, Ellie Fratt, Leann Mount, Kelly McIntosh, Jacob Cotton, Alison A. Bertuch, Elissa Furutani, Winfred C. Wang, Jordan Larson, Akiko Shimamura, Rabi Hanna, Leah Cheng, Sara Loveless, Ashley Galvin, Maggie Malsch, Kasiani C. Myers
Publikováno v:
Blood. 132:3871-3871
The Shwachman-Diamond Syndrome Registry (SDSR) was established in December 2008 with the goal of understanding the natural history and biology of SDS to improve the lives of people with SDS. The SDSR has enrolled 220 patients with biallelic SBDS muta