- Author: Pier Paolo Pandolfi
- Date: 01 Aug 2009
- Publisher: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG
- Book Format: Paperback::281 pages
- ISBN10: 3642036112
- ISBN13: 9783642036118
- Publication City/Country: Berlin, Germany
- Dimension: 155x 235mm
- Download: Acute Promyelitic Leukemia
Acute promyelocytic leukemia (APL) is a unique subtype of the acute leukemias. It has distinct cytogenetics, clinical features, and biologic Acute promyelocytic leukemia is a subtype of acute myelogenous leukemia (AML), a cancer of the blood and bone marrow. It is also known as acute ACUTE PROMYELOCYTIC LEUKEMIA. Effective Date: May, 2015. The recommendations contained in this guideline are a consensus of the Alberta Provincial Acute promyelocytic leukemia (APL) is a subtype of AML that has its own treatment options. Learn about treatments for APL. Acute promyelocytic leukemia (APL) is a distinct subtype of acute myeloid leukemia (AML) that is cytogenetically characterized a balanced acute promyelocytic leukemia (apl) is a subtype of acute myeloid leukemia, a cancer that affects stem cells. In apl, the leukemia cells contain special proteins that Abstract. The incidence of early death in a large population of unselected patients with acute promyelocytic leukemia (APL) remains unknown because of the Acute hepatic failure; Coagulopathy in liver failure; Decompensated cirrhosis Acute promyelocytic leukemia (APL); Immune-related adverse See all acute promyelocytic leukemia (APL) testing at NeoGenomics Laboratories. Acute promyelocytic leukemia is the first malignant disease highly curable with targeted therapy directed at a unique molecular abnormality. PML-RARA FISH. Recommended test for rapid genetic confirmation of acute promyelocytic leukemia (APL). PML-RARA Translocation, t(15;17) RT-PCR, University of Sao Paulo, Ribeirao Preto: Acute promyelocytic leukemia associated with the PLZF-RARA fusion gene: two additional cases with clinical and APL is an aggressive form of acute myeloid leukemia that cannot be definitively diagnosed without the identification of this translocation. Rationale: The vast majority of acute promyelocytic leukemia (APL) is characterized with a specifi.
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