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Valeria Biggio

Researcher at French Institute of Health and Medical Research

Publications -  10
Citations -  1026

Valeria Biggio is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Leukemia & CEBPA. The author has an hindex of 8, co-authored 10 publications receiving 973 citations. Previous affiliations of Valeria Biggio include university of lille.

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Cooperating gene mutations in acute myeloid leukemia: a review of the literature

TL;DR: This nonexhaustive review aims to show how gene mutations interact with each other, how they contribute to refine prognosis and how they can be useful for risk-adapted therapeutic management of AML patients.
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Prevalence, clinical profile, and prognosis of NPM mutations in AML with normal karyotype.

TL;DR: NPM mutations were detected in 47% of patients and were associated with a high white blood cell count, involvement of the monocytic lineage (M4/M5), and a decreased prevalence of CEBPA mutations.
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CEBPA point mutations in hematological malignancies.

TL;DR: Systematic analysis of CEBPA mutations, in addition to that of alterations in master genes of hematopoiesis, may be useful to assess the prognosis of AML particularly in patients belonging to the ‘intermediate’ prognostic subgroup of MRC classification.
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Indoleamine 2,3-dioxygenase activity of acute myeloid leukemia cells can be measured from patients’ sera by HPLC and is inducible by IFN-γ

TL;DR: In patients with acute myeloid leukemia (AML), the serum kynurenine/tryptophan ratio (Kyn/Trp) was raised, suggesting a higher IDO activity than in healthy people, providing a tool for future clinical testing of IDO-blocking drugs.