Lista de obras - Alice Marceau-Renaut - Dominio Público Uruguay

Classification of CEBPA mutated acute myeloid leukemia by GATA2 mutations.

artículo científico publicado en 2015

Clinical relevance of IDH1/2 mutant allele burden during follow-up in acute myeloid leukemia. A study by the French ALFA group.

artículo científico publicado en 2018

Clinico-Biological Features and Clonal Hematopoiesis in Patients with Severe COVID-19

scientific article published on 21 July 2020

Clofarabine Improves Relapse-Free Survival of Acute Myeloid Leukemia in Younger Adults with Micro-Complex Karyotype

scientific article published on 30 December 2019

Clonal interference of signaling mutations holds prognostic relevance in core binding factor acute myeloid leukemia.

artículo científico publicado en 2018

Comprehensive molecular landscape in patients older than 80 years old diagnosed with acute myeloid leukemia: a study of the French Hauts-de-France AML observatory

article

Comprehensive mutational profiling of core binding factor acute myeloid leukemia

artículo científico publicado en 2016

Detection of a new heterozygous germline ETV6 mutation in a case with hyperdiploid acute lymphoblastic leukemia

artículo científico publicado en 2017

Down-syndrome-like acute megakaryoblastic leukemia in a patient with Cornelia de Lange syndrome

artículo científico publicado en 2017

Familial myeloid malignancies with germline TET2 mutation

scientific article published on 11 December 2019

Genetic analysis of therapy-related myeloid neoplasms occurring after intensive treatment for acute promyelocytic leukemia

artículo científico publicado en 2018

IDH1/2 but not DNMT3A mutations are suitable targets for minimal residual disease monitoring in acute myeloid leukemia patients: a study by the Acute Leukemia French Association

artículo científico publicado en 2015

Impact of Wilms' tumor 1 expression on outcome of patients undergoing allogeneic stem cell transplantation for AML

artículo científico publicado en 2017

Inherited transmission of the CSF3R T618I mutational hotspot in familial chronic neutrophilic leukemia

scientific article published on 01 December 2019

Minimal residual disease monitoring in t(8;21) acute myeloid leukemia based on RUNX1-RUNX1T1 fusion quantification on genomic DNA

artículo científico publicado en 2014

Molecular prognostic factors in acute myeloid leukemia receiving first-line therapy with azacitidine

artículo científico publicado en 2015

Mutation analysis of TET2, IDH1, IDH2 and ASXL1 in chronic myeloid leukemia

artículo científico publicado en 2011

Myelodysplastic syndrome (MDS) with isolated trisomy 8: a type of MDS frequently associated with myeloproliferative features? A report by the Groupe Francophone des Myélodysplasies

scientific article published on 13 July 2018

Outcomes and mutational analysis of patients with lower-risk non-del5q myelodysplastic syndrome treated with antithymocyte globulin with or without ciclosporine A

scientific article published on 29 May 2018

Polycomb repressive complex 2 haploinsufficiency identifies a high-risk subgroup of pediatric acute myeloid leukemia

artículo científico publicado en 2018

Postinduction Minimal Residual Disease Predicts Outcome and Benefit From Allogeneic Stem Cell Transplantation in Acute Myeloid Leukemia With NPM1 Mutation: A Study by the Acute Leukemia French Association Group.

artículo científico publicado en 2016

Posttransplantation relapse of pediatric chronic myelomonocytic leukemia cured using donor lymphocyte infusion.

artículo científico publicado en 2017

Prognosis and monitoring of core-binding factor acute myeloid leukemia: current and emerging factors

artículo científico publicado en 2014

Quantification of EVI1 transcript levels in acute myeloid leukemia by RT-qPCR analysis: A study by the ALFA Group.

artículo científico publicado en 2015

Restoration of hematopoiesis in a case of myelodysplastic syndrome associated with systemic lupus erythematosus treated with rituximab

artículo científico publicado en 2015

The stem cell-associated gene expression signature allows risk stratification in pediatric acute myeloid leukemia

scientific article published on 08 August 2018

Lista de obras de Alice Marceau-Renaut

Classification of CEBPA mutated acute myeloid leukemia by GATA2 mutations.

Clinical relevance of IDH1/2 mutant allele burden during follow-up in acute myeloid leukemia. A study by the French ALFA group.

Clinico-Biological Features and Clonal Hematopoiesis in Patients with Severe COVID-19

Clofarabine Improves Relapse-Free Survival of Acute Myeloid Leukemia in Younger Adults with Micro-Complex Karyotype

Clonal interference of signaling mutations holds prognostic relevance in core binding factor acute myeloid leukemia.

Comprehensive molecular landscape in patients older than 80 years old diagnosed with acute myeloid leukemia: a study of the French Hauts-de-France AML observatory

Comprehensive mutational profiling of core binding factor acute myeloid leukemia

Detection of a new heterozygous germline ETV6 mutation in a case with hyperdiploid acute lymphoblastic leukemia

Down-syndrome-like acute megakaryoblastic leukemia in a patient with Cornelia de Lange syndrome

Familial myeloid malignancies with germline TET2 mutation

Genetic analysis of therapy-related myeloid neoplasms occurring after intensive treatment for acute promyelocytic leukemia

IDH1/2 but not DNMT3A mutations are suitable targets for minimal residual disease monitoring in acute myeloid leukemia patients: a study by the Acute Leukemia French Association

Impact of Wilms' tumor 1 expression on outcome of patients undergoing allogeneic stem cell transplantation for AML

Inherited transmission of the CSF3R T618I mutational hotspot in familial chronic neutrophilic leukemia

Minimal residual disease monitoring in t(8;21) acute myeloid leukemia based on RUNX1-RUNX1T1 fusion quantification on genomic DNA

Molecular prognostic factors in acute myeloid leukemia receiving first-line therapy with azacitidine

Mutation analysis of TET2, IDH1, IDH2 and ASXL1 in chronic myeloid leukemia

Myelodysplastic syndrome (MDS) with isolated trisomy 8: a type of MDS frequently associated with myeloproliferative features? A report by the Groupe Francophone des Myélodysplasies

Outcomes and mutational analysis of patients with lower-risk non-del5q myelodysplastic syndrome treated with antithymocyte globulin with or without ciclosporine A

Polycomb repressive complex 2 haploinsufficiency identifies a high-risk subgroup of pediatric acute myeloid leukemia

Postinduction Minimal Residual Disease Predicts Outcome and Benefit From Allogeneic Stem Cell Transplantation in Acute Myeloid Leukemia With NPM1 Mutation: A Study by the Acute Leukemia French Association Group.

Posttransplantation relapse of pediatric chronic myelomonocytic leukemia cured using donor lymphocyte infusion.

Prognosis and monitoring of core-binding factor acute myeloid leukemia: current and emerging factors

Quantification of EVI1 transcript levels in acute myeloid leukemia by RT-qPCR analysis: A study by the ALFA Group.

Restoration of hematopoiesis in a case of myelodysplastic syndrome associated with systemic lupus erythematosus treated with rituximab

The stem cell-associated gene expression signature allows risk stratification in pediatric acute myeloid leukemia