Lista de obras -

Association of 17q24.2-q24.3 deletions with recognizable phenotype and short telomeres.

artículo científico publicado en 2018

Comparison of minimal residual disease levels in bone marrow and peripheral blood in adult acute lymphoblastic leukemia

artículo científico publicado en 2019

Distinct bilineal leukemia immunophenotypes are not genetically determined

artículo científico publicado en 2016

ETV6/RUNX1-like acute lymphoblastic leukemia: A novel B-cell precursor leukemia subtype associated with the CD27/CD44 immunophenotype.

artículo científico publicado en 2017

Is Next-Generation Sequencing the way to go for Residual Disease Monitoring in Acute Lymphoblastic Leukemia?

artículo científico publicado en 2017

Minimal residual disease in adult ALL: technical aspects and implications for correct clinical interpretation

artículo científico publicado en 2017

Minimal residual disease in adult ALL: technical aspects and implications for correct clinical interpretation.

artículo científico publicado en 2017

Next-Generation Sequencing Technology to Identify Minimal Residual Disease in Lymphoid Malignancies

artículo científico publicado en 2021

Next-generation amplicon TRB locus sequencing can overcome limitations of flow-cytometric Vβ expression analysis and confirms clonality in all T-cell prolymphocytic leukemia cases

artículo científico publicado en 2018

Next-generation sequencing indicates false-positive MRD results and better predicts prognosis after SCT in patients with childhood ALL.

artículo científico publicado en 2017

Next-generation sequencing of immunoglobulin gene rearrangements for clonality assessment: a technical feasibility study by EuroClonality-NGS

scientific article published on 13 June 2019

Polyclonal, newly derived T cells with low expression of inhibitory molecule PD-1 in tonsils define the phenotype of lymphocytes in children with Periodic Fever, Aphtous Stomatitis, Pharyngitis and Adenitis (PFAPA) syndrome.

artículo científico publicado en 2015

Quality control and quantification in IG/TR next-generation sequencing marker identification: protocols and bioinformatic functionalities by EuroClonality-NGS

scientific article published on 21 June 2019

Standardized flow cytometry for highly sensitive MRD measurements in B-cell acute lymphoblastic leukemia

artículo científico publicado en 2016

Standardized next-generation sequencing of immunoglobulin and T-cell receptor gene recombinations for MRD marker identification in acute lymphoblastic leukaemia; a EuroClonality-NGS validation study

scientific article published on 26 June 2019

The TREC/KREC assay for the diagnosis and monitoring of patients with DiGeorge syndrome.

artículo científico publicado en 2014

The predictive strength of next-generation sequencing MRD detection for relapse compared with current methods in childhood ALL.

artículo científico publicado en 2015

Wilms tumor gene 1 (WT1), TP53, RAS/BRAF and KIT aberrations in testicular germ cell tumors.

artículo científico publicado en 2016

Lista de obras de

Association of 17q24.2-q24.3 deletions with recognizable phenotype and short telomeres.

Comparison of minimal residual disease levels in bone marrow and peripheral blood in adult acute lymphoblastic leukemia

Distinct bilineal leukemia immunophenotypes are not genetically determined

ETV6/RUNX1-like acute lymphoblastic leukemia: A novel B-cell precursor leukemia subtype associated with the CD27/CD44 immunophenotype.

Is Next-Generation Sequencing the way to go for Residual Disease Monitoring in Acute Lymphoblastic Leukemia?

Minimal residual disease in adult ALL: technical aspects and implications for correct clinical interpretation

Minimal residual disease in adult ALL: technical aspects and implications for correct clinical interpretation.

Next-Generation Sequencing Technology to Identify Minimal Residual Disease in Lymphoid Malignancies

Next-generation amplicon TRB locus sequencing can overcome limitations of flow-cytometric Vβ expression analysis and confirms clonality in all T-cell prolymphocytic leukemia cases

Next-generation sequencing indicates false-positive MRD results and better predicts prognosis after SCT in patients with childhood ALL.

Next-generation sequencing of immunoglobulin gene rearrangements for clonality assessment: a technical feasibility study by EuroClonality-NGS

Polyclonal, newly derived T cells with low expression of inhibitory molecule PD-1 in tonsils define the phenotype of lymphocytes in children with Periodic Fever, Aphtous Stomatitis, Pharyngitis and Adenitis (PFAPA) syndrome.

Quality control and quantification in IG/TR next-generation sequencing marker identification: protocols and bioinformatic functionalities by EuroClonality-NGS

Standardized flow cytometry for highly sensitive MRD measurements in B-cell acute lymphoblastic leukemia

Standardized next-generation sequencing of immunoglobulin and T-cell receptor gene recombinations for MRD marker identification in acute lymphoblastic leukaemia; a EuroClonality-NGS validation study

The TREC/KREC assay for the diagnosis and monitoring of patients with DiGeorge syndrome.

The predictive strength of next-generation sequencing MRD detection for relapse compared with current methods in childhood ALL.

Wilms tumor gene 1 (WT1), TP53, RAS/BRAF and KIT aberrations in testicular germ cell tumors.