Irene Luna

Valencia, VC 46026, Spain

Last Updated: 09/26/2026

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Found 24 publications

Detection of clinically relevant variants in the TP53 gene below 10% allelic frequency: A multicenter study by ERIC, the European Research Initiative on CLL.

Detection of clinically relevant variants in the TP53 gene below 10% allelic frequency: A multicenter study by ERIC, the European Research Initiative on CLL.

Journal: HemaSphere

Published: July 11, 2024

WHO/ICC Classification for Myelodysplastic Neoplasms/Syndromes Performs Better for Subtype Cytomorphological Diagnosis?

WHO/ICC Classification for Myelodysplastic Neoplasms/Syndromes Performs Better for Subtype Cytomorphological Diagnosis?

Journal: Diagnostics (Basel, Switzerland)

Published: June 24, 2024

Cytogenetic Assessment and Risk Stratification in Myelofibrosis with Optical Genome Mapping.

Cytogenetic Assessment and Risk Stratification in Myelofibrosis with Optical Genome Mapping.

Journal: Cancers

Published: April 15, 2023

Panel Sequencing for Clinically Oriented Variant Screening and Copy Number Detection in Chronic Lymphocytic Leukemia Patients.

Panel Sequencing for Clinically Oriented Variant Screening and Copy Number Detection in Chronic Lymphocytic Leukemia Patients.

Journal: Diagnostics (Basel, Switzerland)

Published: March 21, 2022

Adoptive transfer of ex vivo expanded SARS-CoV-2-specific cytotoxic lymphocytes: A viable strategy for COVID-19 immunosuppressed patients?

Adoptive transfer of ex vivo expanded SARS-CoV-2-specific cytotoxic lymphocytes: A viable strategy for COVID-19 immunosuppressed patients?

Journal: Transplant infectious disease : an official journal of the Transplantation Society

Published: February 12, 2021

Proposed global prognostic score for systemic mastocytosis: a retrospective prognostic modelling study.

Proposed global prognostic score for systemic mastocytosis: a retrospective prognostic modelling study.

Journal: The Lancet. Haematology

Published: August 08, 2020

Lineage switch from B lymphoblastic leukemia with KMT2A-rearranged to mixed-phenotype acute leukemia under daratumumab.

Lineage switch from B lymphoblastic leukemia with KMT2A-rearranged to mixed-phenotype acute leukemia under daratumumab.

Journal: Blood research

Published: March 29, 2020

Partial T Cell-Depleted Peripheral Blood Stem Cell Transplantation from HLA-Identical Sibling Donors for Patients with Severe Aplastic Anemia.

Partial T Cell-Depleted Peripheral Blood Stem Cell Transplantation from HLA-Identical Sibling Donors for Patients with Severe Aplastic Anemia.

Journal: Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation

Published: June 07, 2019

RNA Sequencing Analysis for the Identification of a PCM1/PDGFRB Fusion Gene Responsive to Imatinib.

RNA Sequencing Analysis for the Identification of a PCM1/PDGFRB Fusion Gene Responsive to Imatinib.

Journal: Acta haematologica

Published: December 05, 2018

Negative impact on clinical outcome of the mutational co-occurrence of SF3B1 and DNMT3A in refractory anemia with ring sideroblasts (RARS).

Negative impact on clinical outcome of the mutational co-occurrence of SF3B1 and DNMT3A in refractory anemia with ring sideroblasts (RARS).

Journal: Leukemia & lymphoma

Published: October 25, 2016

Validation of R-MIPI and prognostic value of immunoglobulin light chain restriction in mantle cell lymphoma.

Validation of R-MIPI and prognostic value of immunoglobulin light chain restriction in mantle cell lymphoma.

Journal: British journal of haematology

Published: April 30, 2016

Impact of azacitidine on red blood cell alloimmunisation in myelodysplastic syndrome.

Impact of azacitidine on red blood cell alloimmunisation in myelodysplastic syndrome.

Journal: Blood transfusion = Trasfusione del sangue

Published: January 18, 2016

Showing 1-12 of 24

Last Updated: 09/26/2026