AML

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Related to Acute myeloid leukaemia: Chronic myeloid leukaemia, Acute lymphoblastic leukaemia

AML

McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.

AML

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References in periodicals archive ?
Genetic testing incorporating both cytogenetic karyotyping and molecular analysis has an important role in defining and classifying AML patients.10 Specific cytogenetic and molecular features defining specific disease entities permit classification of AML patients.11 These genetic molecular markers help predict the likelihood of attaining a complete remission and subsequent disease-free survival in patients of acute myeloid leukaemia.4 Information regarding the genetic landscape of AML and its impact on prognosis is important in guiding treatment decisions.1
The most common subtype was acute myeloid leukaemia with maturation 183(33.6%).
Pelliniemi, "Spontaneous remission in acute myeloid leukaemia," British Journal of Haematology, vol.
Grimwade, "The clinical significance of cytogenetic abnormalities in acute myeloid leukaemia," Best Practice & Research Clinical Haematology, vol.
Material and Methods: Retrospective review of documents of patient diagnosed to have acute myeloid leukaemia on bone marrow aspiration was done.
Acute myeloid leukaemia in children: experience at a tertiary care facility of Pakistan.
"Our results also identify drug-resistant mutations in FLT3 that represent high-value targets for future drug development, and will hopefully rekindle interest in developing potent FLT3 inhibitors for the treatment of acute myeloid leukaemia," he stated.
The centre has a particular focus on acute myeloid leukaemia (AML) and conducts pre-clinical testing of novel agents that could lead to new treatments for the disease.
Toma Fund founder Andrea, who lost her son Jordan after a 19-month battle with acute myeloid leukaemia, thought Nina was just calling about a regular fundraiser.
The clinical spectrum of adult acute myeloid leukaemia associated with core binding factor translocations.
The draft guidance affects patients who are not suitable for stem cell transplation, who have intermediate-2 and high risk MDS, chronic myelomonocytic leukaemia and acute myeloid leukaemia.

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