Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Adrianna Vlachos"'
Autor:
Katie Bergstrom, Yigal Dror, Kathleen Overholt, Melissa J. Rose, Paul Castillo, Beth A Carella, Kristin A. Shimano, Bonnie W Lau, James N. Huang, Larisa Broglie, Evan Shereck, Steven W. Allen, Timothy S. Olson, Jessica Boklan, Anupama Narla, Catherine E. McGuinn, Taizo A. Nakano, Adrianna Vlachos, Marcin W. Wlodarski, Amy E. Geddis, Nicholas J. Gloude, Jill L. O. de Jong, Anjali Sharathkumar, Jennifer A. Rothman, Akiko Shimamura, Alison A. Bertuch
Publikováno v:
American journal of hematologyREFERENCES. 96(11)
The North American Pediatric Aplastic Anemia Consortium (NAPAAC) is a group of pediatric hematologist-oncologists, hematopathologists, and bone marrow transplant physicians from 46 institutions in North America with interest and expertise in aplastic
Autor:
Ravi Sharaf, Blanche P. Alter, Philip S. Rosenberg, Kenan Onel, Adrianna Vlachos, Eva Atsidaftos, Jeffrey M. Lipton, Jessica Kang
Publikováno v:
Blood. 132:2205-2208
TO THE EDITOR: Inherited bone marrow failure syndromes (IBMFSs), characterized by bone marrow failure and developmental anomalies, are among a group of rare cancer predisposition syndromes. As illustrated by Fanconi anemia (FA),[1][1] the unique biol
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:
Maryam Hussain, Maria Florento, Pooja Desai, Jeffrey M. Lipton, Adrianna Vlachos, Christine Louise Sardo Molmenti, Eva Atsidaftos
Publikováno v:
Pediatric bloodcancerREFERENCES. 68(8)
Diamond Blackfan anemia (DBA) is a rare inherited bone marrow failure syndrome characterized by red cell failure, congenital anomalies, poor linear growth, and cancer predisposition. Two previous analyses from the Diamond Blackfan Anemia Registry hav
Autor:
Julien Papoin, Brian M. Dulmovits, Jeffrey M. Lipton, Hongxia Yan, Narla Mohandas, Nan Wang, Christopher D. Hillyer, Steven A. Carr, Lydie Da Costa, Ryan Ashley, Meagan E. Olive, Naomi Taylor, Adrianna Vlachos, Sandrina Kinet, Namrata D. Udeshi, Lionel Blanc, Anupama Narla, John Hale
Publikováno v:
Journal of Clinical Investigation
Journal of Clinical Investigation, American Society for Clinical Investigation, 2020, 130 (4), pp.2097-2110. ⟨10.1172/JCI132284⟩
J Clin Invest
Journal of Clinical Investigation, American Society for Clinical Investigation, 2020, 130 (4), pp.2097-2110. ⟨10.1172/JCI132284⟩
J Clin Invest
Despite the effective clinical use of steroids for the treatment of Diamond Blackfan anemia (DBA), the mechanisms through which glucocorticoids regulate human erythropoiesis remain poorly understood. We report that the sensitivity of erythroid differ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3faf6bf23c286f3a82c2a9745a0a75a
https://hal.archives-ouvertes.fr/hal-03016140
https://hal.archives-ouvertes.fr/hal-03016140
Autor:
Yael T. Harris, Jeffrey M. Lipton, Amit Lahoti, Phyllis W. Speiser, Adrianna Vlachos, Evangelia Atsidaftos
Publikováno v:
Pediatric Blood & Cancer. 63:306-312
Objective Diamond Blackfan anemia (DBA) is a rare inherited bone marrow failure syndrome. The mainstays of treatment involve chronic red cell transfusions, long-term glucocorticoid therapy, and stem cell transplantation. Systematic data concerning en
Autor:
Roderick Skinner, Jean Hugues Dalle, Michael A. Pulsipher, Jeffrey M. Lipton, Carmem Bonfim, Dorine Bresters, Adrianna Vlachos, Jakub Tolar, Parinda A. Mehta, Sharon A. Savage, Andrew C. Dietz, Blanche P. Alter, John E. Wagner, Farid Boulad, Josu de la Fuente, Christine Duncan, K. Scott Baker
Publikováno v:
Biology of Blood and Marrow Transplantation, 23(9), 1422-1428
Patients with inherited bone marrow failure syndromes (IBMFS), such as Fanconi anemia (FA), dyskeratosis congenita (DC), or Diamond Blackfan anemia (DBA), can have hematologic manifestations cured through hematopoietic cell transplantation (HCT). Sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a16133e2c0d5a19fef7ffebb14531d2
https://hdl.handle.net/1887/94638
https://hdl.handle.net/1887/94638
Autor:
Jeffrey M. Lipton, Dorine Bresters, Adrianna Vlachos, Parinda A. Mehta, K. Scott Baker, Andrew C. Dietz, Sharon A. Savage, Blanche P. Alter, Christine Duncan, Michael A. Pulsipher, Carmem Bonfim, Jean Hugues Dalle, Jakub Tolar, Josu de la Fuente, Farid Boulad, John E. Wagner
Publikováno v:
Biology of Blood and Marrow Transplantation, 23(5), 726-735
Fanconi anemia (FA), dyskeratosis congenita (DC), and Diamond Blackfan anemia (DBA) are 3 of the most common inherited bone marrow failure syndromes (IBMFS), in which the hematologic manifestations can be cured with hematopoietic cell transplantation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aec1306bdc68392a10ca2ea96ff46f45
https://hdl.handle.net/1887/94635
https://hdl.handle.net/1887/94635
Autor:
Kelly A. O'Brien, Crystiana A. Tsujiura, David M. Bodine, Adrianna Vlachos, Abdel G. Elkahloun, Xiuli An, Lionel Blanc, Eva Atsidaftos, Steven R. Ellis, Jens Lichtenberg, Jason E. Farrar, Jeffrey M. Lipton, Stacie M. Anderson
Publikováno v:
Blood. 129(23)
Diamond-Blackfan anemia (DBA) is a congenital bone marrow failure syndrome characterized by erythroid hypoplasia, usually without perturbation of other hematopoietic lineages. Approximately 65% of DBA patients with autosomal dominant inheritance have
Publikováno v:
Expert Review of Hematology. 7:359-372
Diamond Blackfan anemia (DBA) is an inherited bone marrow failure syndrome. As with the other rare inherited bone marrow failure syndromes, the study of these disorders provides important insights into basic biology and, in the case of DBA, ribosome