Lista de obras - Arnaud Petit - Dominio Público Uruguay

ARID5B, IKZF1 and non-genetic factors in the etiology of childhood acute lymphoblastic leukemia: the ESCALE study.

artículo científico publicado en 2015

Acute Myeloid Leukemia With Central Nervous System Involvement in Children: Experience From the French Protocol Analysis ELAM02.

artículo científico publicado en 2017

Acute megakaryoblastic leukemia (excluding Down syndrome) remains an acute myeloid subgroup with inferior outcome in the French ELAM02 trial

artículo científico publicado en 2018

Age-related clinical and biological features of PTEN abnormalities in T-cell acute lymphoblastic leukaemia.

artículo científico publicado en 2017

An innovative pedagogic course combining video and simulation to teach medical students about pediatric cardiopulmonary arrest: a prospective controlled study.

artículo científico publicado en 2016

Appendicitis in a Neutropenic Patient: A Multicentric Retrospective Study.

artículo científico publicado en 2017

Characterization of novel genomic alterations and therapeutic approaches using acute megakaryoblastic leukemia xenograft models

artículo científico publicado en 2012

Childhood acute leukemia, early common infections, and allergy: The ESCALE Study

artículo científico publicado en 2010

Childhood acute lymphoblastic leukaemia and indicators of early immune stimulation: the Estelle study (SFCE)

artículo científico publicado en 2015

Childhood diagnosis of genetic thrombocytopenia with mutation in the ankyrine repeat domain 26 gene

artículo científico publicado en 2015

Clinical and biological features of PTPN2-deleted adult and pediatric T-cell acute lymphoblastic leukemia

scientific article published on 01 July 2019

Clinical impact of NOTCH1 and/or FBXW7 mutations, FLASH deletion, and TCR status in pediatric T-cell lymphoblastic lymphoma

artículo científico publicado en 2012

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

artículo científico publicado en 2018

Comprehensive mutational profiling of core binding factor acute myeloid leukemia

artículo científico publicado en 2016

Congenital Disseminated Extrarenal Malignant Rhabdoid Tumor

artículo científico publicado en 2015

Contribution of HLA-A/B/C/DRB1/DQB1 common haplotypes to donor search outcome in unrelated hematopoietic stem cell transplantation

scientific article published on 12 April 2011

Disseminated fusarium infection in two neutropenic children

artículo científico publicado en 2005

ETO2-GLIS2 Hijacks Transcriptional Complexes to Drive Cellular Identity and Self-Renewal in Pediatric Acute Megakaryoblastic Leukemia.

artículo científico publicado en 2017

Evidence-based ideas for pediatric residents' training

artículo científico publicado en 2017

Excellent prognosis of late relapses of ETV6/RUNX1-positive childhood acute lymphoblastic leukemia: lessons from the FRALLE 93 protocol

artículo científico publicado en 2012

Extensive molecular mapping of TCRα/δ- and TCRβ-involved chromosomal translocations reveals distinct mechanisms of oncogene activation in T-ALL.

artículo científico publicado en 2012

French "real life" experience of clofarabine in children with refractory or relapsed acute lymphoblastic leukaemia

artículo científico publicado en 2012

Frequent ASXL2 mutations in acute myeloid leukemia patients with t(8;21)/RUNX1-RUNX1T1 chromosomal translocations.

artículo científico publicado en 2014

Functional analysis of the NUP98-CCDC28A fusion protein

artículo científico publicado en 2011

Genetic polymorphisms and childhood acute lymphoblastic leukemia: GWAS of the ESCALE study (SFCE)

article

Google Glass for Residents Dealing With Pediatric Cardiopulmonary Arrest: A Randomized, Controlled, Simulation-Based Study

artículo científico publicado en 2017

Growth deceleration in children treated with imatinib for chronic myeloid leukaemia

artículo científico publicado en 2014

High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia.

scientific article published on 06 December 2012

Imatinib is effective in children with previously untreated chronic myelogenous leukemia in early chronic phase: results of the French national phase IV trial

artículo científico

Impact of early molecular response in children with chronic myeloid leukemia treated in the French Glivec phase 4 study.

artículo científico publicado en 2014

Impact of therapy in a cohort of unselected children with Down Syndrome-associated Acute Lymphoblastic Leukaemia

article published in 2015

Impact on long-term OS of conditioning regimen in allogeneic BMT for children with AML in first CR: TBI+CY versus BU+CY: a report from the Société Française de Greffe de Moelle et de Thérapie Cellulaire.

artículo científico publicado en 2013

In hematopoietic cells with a germline mutation of CBL, loss of heterozygosity is not a signature of juvenile myelo-monocytic leukemia.

artículo científico publicado en 2013

International retrospective analysis of 73 cases of invasive fusariosis treated with voriconazole.

artículo científico publicado en 2010

Is there a risk of steroid-induced adrenal deficit after induction treatment of acute lymphoblastic leukemia?

artículo científico publicado en 2010

Juvenile myelomonocytic leukemia displays mutations in components of the RAS pathway and the PRC2 network.

artículo científico publicado en 2015

Loss of RASGRP1 in humans impairs T-cell expansion leading to Epstein-Barr virus susceptibility.

artículo científico publicado en 2017

Malignant Ectomesenchymoma: A Potential Pitfall of Diagnosis in the Spectrum of Pediatric Small Blue Round Cell Tumors

artículo científico publicado en 2017

Maternal reproductive history, fertility treatments and folic acid supplementation in the risk of childhood acute leukemia: the ESTELLE study

artículo científico publicado en 2014

NUP98 is rearranged in 3.8% of pediatric AML forming a clinical and molecular homogenous group with a poor prognosis

artículo científico publicado en 2016

NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique.

artículo científico publicado en 2006

NUP98–HMGB3: a novel oncogenic fusion

artículo científico publicado en 2009

NUP98–NSD1 fusion by insertion in acute myeloblastic leukemia

article published in 2008

Oncogenetic mutations combined with MRD improve outcome prediction in pediatric T-cell acute lymphoblastic leukemia.

artículo científico publicado en 2017

Ontogenic Changes in Hematopoietic Hierarchy Determine Pediatric Specificity and Disease Phenotype in Fusion Oncogene-Driven Myeloid Leukemia

scientific article published on 29 October 2019

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

artículo científico publicado en 2018

RET fusion genes are associated with chronic myelomonocytic leukemia and enhance monocytic differentiation.

artículo científico publicado en 2012

Rapid childhood T-ALL growth in xenograft models correlates with mature phenotype and NF-κB pathway activation but not with poor prognosis

artículo científico publicado en 2014

Receptor kinase profiles identify a rationale for multitarget kinase inhibition in immature T-ALL.

artículo científico publicado en 2012

SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemia

artículo científico publicado en 2014

Scopulariopsis brevicaulis abscess in a child treated for myeloblastic leukaemia

artículo científico publicado en 2011

Screening of ETO2-GLIS2-induced Super Enhancers identifies targetable cooperative dependencies in acute megakaryoblastic leukemia

artículo científico publicado en 2022

Splenic infarction in a child revealing chronic myeloid leukemia

scientific article published on 27 January 2012

TCRα rearrangements identify a subgroup of NKL-deregulated adult T-ALLs associated with favorable outcome.

artículo científico publicado en 2017

TLX homeodomain oncogenes mediate T cell maturation arrest in T-ALL via interaction with ETS1 and suppression of TCRα gene expression

artículo científico publicado en 2012

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

scientific article published on 08 August 2018

Tolerance to arsenic trioxide combined with all-trans-retinoic acid in children with acute promyelocytic leukaemia in France

scientific article published on 06 December 2019

Unlike ASXL1 and ASXL2 mutations, ASXL3 mutations are rare events in acute myeloid leukemia with t(8;21)

artículo científico publicado en 2015

Usefulness of ß-D-glucan for diagnosis and follow-up of invasive candidiasis in onco-haematological patients

artículo científico publicado en 2018

Vinblastine in the treatment of children and adolescents with refractory immune thrombocytopenia

artículo científico publicado en 2011

[Inherited thrombocytopenias].

artículo científico publicado en 2010

[Intracardial migration of a bullet: diagnosis and management]

artículo científico publicado en 2002

[Newly formed French residents in pediatrics are not well prepared for conducting pediatric resuscitation after medical school]

artículo científico publicado en 2016

Lista de obras de Arnaud Petit

ARID5B, IKZF1 and non-genetic factors in the etiology of childhood acute lymphoblastic leukemia: the ESCALE study.

Acute Myeloid Leukemia With Central Nervous System Involvement in Children: Experience From the French Protocol Analysis ELAM02.

Acute megakaryoblastic leukemia (excluding Down syndrome) remains an acute myeloid subgroup with inferior outcome in the French ELAM02 trial

Age-related clinical and biological features of PTEN abnormalities in T-cell acute lymphoblastic leukaemia.

An innovative pedagogic course combining video and simulation to teach medical students about pediatric cardiopulmonary arrest: a prospective controlled study.

Appendicitis in a Neutropenic Patient: A Multicentric Retrospective Study.

Characterization of novel genomic alterations and therapeutic approaches using acute megakaryoblastic leukemia xenograft models

Childhood acute leukemia, early common infections, and allergy: The ESCALE Study

Childhood acute lymphoblastic leukaemia and indicators of early immune stimulation: the Estelle study (SFCE)

Childhood diagnosis of genetic thrombocytopenia with mutation in the ankyrine repeat domain 26 gene

Clinical and biological features of PTPN2-deleted adult and pediatric T-cell acute lymphoblastic leukemia

Clinical impact of NOTCH1 and/or FBXW7 mutations, FLASH deletion, and TCR status in pediatric T-cell lymphoblastic lymphoma

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

Comprehensive mutational profiling of core binding factor acute myeloid leukemia

Congenital Disseminated Extrarenal Malignant Rhabdoid Tumor

Contribution of HLA-A/B/C/DRB1/DQB1 common haplotypes to donor search outcome in unrelated hematopoietic stem cell transplantation

Disseminated fusarium infection in two neutropenic children

ETO2-GLIS2 Hijacks Transcriptional Complexes to Drive Cellular Identity and Self-Renewal in Pediatric Acute Megakaryoblastic Leukemia.

Evidence-based ideas for pediatric residents' training

Excellent prognosis of late relapses of ETV6/RUNX1-positive childhood acute lymphoblastic leukemia: lessons from the FRALLE 93 protocol

Extensive molecular mapping of TCRα/δ- and TCRβ-involved chromosomal translocations reveals distinct mechanisms of oncogene activation in T-ALL.

French "real life" experience of clofarabine in children with refractory or relapsed acute lymphoblastic leukaemia

Frequent ASXL2 mutations in acute myeloid leukemia patients with t(8;21)/RUNX1-RUNX1T1 chromosomal translocations.

Functional analysis of the NUP98-CCDC28A fusion protein

Genetic polymorphisms and childhood acute lymphoblastic leukemia: GWAS of the ESCALE study (SFCE)

Google Glass for Residents Dealing With Pediatric Cardiopulmonary Arrest: A Randomized, Controlled, Simulation-Based Study

Growth deceleration in children treated with imatinib for chronic myeloid leukaemia

High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia.

Imatinib is effective in children with previously untreated chronic myelogenous leukemia in early chronic phase: results of the French national phase IV trial

Impact of early molecular response in children with chronic myeloid leukemia treated in the French Glivec phase 4 study.

Impact of therapy in a cohort of unselected children with Down Syndrome-associated Acute Lymphoblastic Leukaemia

Impact on long-term OS of conditioning regimen in allogeneic BMT for children with AML in first CR: TBI+CY versus BU+CY: a report from the Société Française de Greffe de Moelle et de Thérapie Cellulaire.

In hematopoietic cells with a germline mutation of CBL, loss of heterozygosity is not a signature of juvenile myelo-monocytic leukemia.

International retrospective analysis of 73 cases of invasive fusariosis treated with voriconazole.

Is there a risk of steroid-induced adrenal deficit after induction treatment of acute lymphoblastic leukemia?

Juvenile myelomonocytic leukemia displays mutations in components of the RAS pathway and the PRC2 network.

Loss of RASGRP1 in humans impairs T-cell expansion leading to Epstein-Barr virus susceptibility.

Malignant Ectomesenchymoma: A Potential Pitfall of Diagnosis in the Spectrum of Pediatric Small Blue Round Cell Tumors

Maternal reproductive history, fertility treatments and folic acid supplementation in the risk of childhood acute leukemia: the ESTELLE study

NUP98 is rearranged in 3.8% of pediatric AML forming a clinical and molecular homogenous group with a poor prognosis

NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique.

NUP98–HMGB3: a novel oncogenic fusion

NUP98–NSD1 fusion by insertion in acute myeloblastic leukemia

Oncogenetic mutations combined with MRD improve outcome prediction in pediatric T-cell acute lymphoblastic leukemia.

Ontogenic Changes in Hematopoietic Hierarchy Determine Pediatric Specificity and Disease Phenotype in Fusion Oncogene-Driven Myeloid Leukemia

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

RET fusion genes are associated with chronic myelomonocytic leukemia and enhance monocytic differentiation.

Rapid childhood T-ALL growth in xenograft models correlates with mature phenotype and NF-κB pathway activation but not with poor prognosis

Receptor kinase profiles identify a rationale for multitarget kinase inhibition in immature T-ALL.

SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemia

Scopulariopsis brevicaulis abscess in a child treated for myeloblastic leukaemia

Screening of ETO2-GLIS2-induced Super Enhancers identifies targetable cooperative dependencies in acute megakaryoblastic leukemia

Splenic infarction in a child revealing chronic myeloid leukemia

TCRα rearrangements identify a subgroup of NKL-deregulated adult T-ALLs associated with favorable outcome.

TLX homeodomain oncogenes mediate T cell maturation arrest in T-ALL via interaction with ETS1 and suppression of TCRα gene expression

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

Tolerance to arsenic trioxide combined with all-trans-retinoic acid in children with acute promyelocytic leukaemia in France

Unlike ASXL1 and ASXL2 mutations, ASXL3 mutations are rare events in acute myeloid leukemia with t(8;21)

Usefulness of ß-D-glucan for diagnosis and follow-up of invasive candidiasis in onco-haematological patients

Vinblastine in the treatment of children and adolescents with refractory immune thrombocytopenia

[Inherited thrombocytopenias].

[Intracardial migration of a bullet: diagnosis and management]

[Newly formed French residents in pediatrics are not well prepared for conducting pediatric resuscitation after medical school]