Aggeliki Daraki
Athens, ESYE31, Greece
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 14 publications
Erdheim-Chester Disease and Acute Myeloid Leukemia with Mutated NPM1 in a Patient with Clonal Hematopoiesis: A Case Report.
Journal: OncoTargets and therapy
Published: August 14, 2020
ASXL1 mutations in AML are associated with specific clinical and cytogenetic characteristics.
Journal: Leukemia & lymphoma
Published: February 08, 2018
Cohesin RAD21 Gene Promoter Methylation in Patients with Chronic Lymphocytic Leukemia.
Journal: Cytogenetic and genome research
Published: January 24, 2018
GSTP1 and CYP2B6 Genetic Polymorphisms and the Risk of Bronchopulmonary Dysplasia in Preterm Neonates.
Journal: American journal of perinatology
Published: January 13, 2017
Polymorphisms and haplotypes of the CYP2B6 detoxification gene in the predisposition of Acute Myeloid Leukemia (AML) and induction of its cytogenetic abnormalities.
Journal: Cancer genetics
Published: June 28, 2016
Association of C609T-Inborn Polymorphism of NAD(P)H: Quinone Oxidoreductase 1 with the Risk of Bronchopulmonary Dysplasia in Preterm Neonates.
Journal: American journal of perinatology
Published: December 20, 2015
Glutathione S-transferase P1 promoter hypermethylation in acute myeloid leukemia: association with A³¹³G germline polymorphism and chromosomal abnormalities.
Journal: Leukemia & lymphoma
Published: February 20, 2014
The G⁵¹⁶T CYP2B6 germline polymorphism affects the risk of acute myeloid leukemia and is associated with specific chromosomal abnormalities.
Journal: PloS one
Published: September 04, 2013
Association of A(313)G glutathione S-transferase P1 germline polymorphism with susceptibility to de novo myelodysplastic syndrome.
Journal: Leukemia & lymphoma
Published: January 03, 2013
Translocation t(5;18)(q35;q21) as a rare nonrandom abnormality in acute myeloid leukemia.
Journal: Cytogenetic and genome research
Published: November 12, 2012
Last Updated: 09/26/2026