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Book Chapter: Prognostic Models for Primary and Secondary Myelofibrosis
Title | Prognostic Models for Primary and Secondary Myelofibrosis |
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Authors | |
Issue Date | 28-Sep-2023 |
Publisher | Springer Nature Singapore |
Abstract | Although patients with primary and secondary myelofibrosis are at risk of disease progression into acute myeloid leukemia, they are heterogenous at presentation and have a highly variable survival. In the last decade, with the rapid expansion of our knowledge in the impact of cytogenetics and molecular makers, these have been, in addition to the traditional clinical parameters, incorporated into different prognostic models. These models not only help in disease prognostication, but they also play an important role in treatment decision making. |
Persistent Identifier | http://hdl.handle.net/10722/341854 |
ISBN |
DC Field | Value | Language |
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dc.contributor.author | Gill, Harinder | - |
dc.contributor.author | Leung, Garret | - |
dc.date.accessioned | 2024-03-26T05:37:42Z | - |
dc.date.available | 2024-03-26T05:37:42Z | - |
dc.date.issued | 2023-09-28 | - |
dc.identifier.isbn | 9789819938094 | - |
dc.identifier.uri | http://hdl.handle.net/10722/341854 | - |
dc.description.abstract | <p>Although patients with primary and secondary myelofibrosis are at risk of disease progression into acute myeloid leukemia, they are heterogenous at presentation and have a highly variable survival. In the last decade, with the rapid expansion of our knowledge in the impact of cytogenetics and molecular makers, these have been, in addition to the traditional clinical parameters, incorporated into different prognostic models. These models not only help in disease prognostication, but they also play an important role in treatment decision making.<br></p> | - |
dc.language | eng | - |
dc.publisher | Springer Nature Singapore | - |
dc.relation.ispartof | Pathogenesis and Treatment of Leukemia | - |
dc.title | Prognostic Models for Primary and Secondary Myelofibrosis | - |
dc.type | Book_Chapter | - |
dc.identifier.doi | 10.1007/978-981-99-3810-0_39 | - |
dc.identifier.eisbn | 9789819938100 | - |