Lista de obras - André Baruchel - Dominio Público Uruguay

A landscape of germline mutations in a cohort of inherited bone marrow failure patients

artículo científico publicado en 2017

Activating mutations in human acute megakaryoblastic leukemia.

artículo científico publicado en 2008

Acute lymphoblastic leukemia in adolescent and young adults: treat as adults or as children?

artículo científico publicado en 2018

An effective modestly intensive re-induction regimen with bortezomib in relapsed or refractory paediatric acute lymphoblastic leukaemia.

artículo científico publicado en 2018

Biallelic inactivation of REV7 is associated with Fanconi anemia

artículo científico publicado en 2016

Biallelic inactivation of REV7 is associated with Fanconi anemia

artículo científico publicado en 2017

Clinical outcome of children with newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia treated between 1995 and 2005.

artículo científico publicado en 2010

Cranial polyneuropathy as the first manifestation of a severe COVID-19 in a child

scientific article published on 24 September 2020

Criteria for evaluating response and outcome in clinical trials for children with juvenile myelomonocytic leukemia

artículo científico publicado en 2015

Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemia

artículo científico publicado en 2010

High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder.

artículo científico publicado en 2009

Identification of distinct molecular phenotypes in acute megakaryoblastic leukemia by gene expression profiling.

artículo científico publicado en 2006

Juvenile myelomonocytic leukaemia and Noonan syndrome.

artículo científico publicado en 2014

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

artículo científico publicado en 2015

MicroRNA-106b~25 cluster is upregulated in relapsed MLL-rearranged pediatric acute myeloid leukemia

artículo científico publicado en 2016

Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions

artículo científico publicado en 2011

Nelarabine for T cell acute lymphoblastic leukemia relapsing after allogeneic hematopoietic stem cell transplantation: an opportunity to improve survival

artículo científico publicado en 2013

Outcome of acute promyelocytic leukemia (APL) in children and adolescents: an analysis in two consecutive trials of the European APL Group.

artículo científico publicado en 2012

Outcomes after induction failure in childhood acute lymphoblastic leukemia

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

When can real-time quantitative RT-PCR effectively define molecular relapse in acute promyelocytic leukemia patients? (Results of the French Belgian Swiss APL Group).

artículo científico publicado en 2009

Lista de obras de André Baruchel

A landscape of germline mutations in a cohort of inherited bone marrow failure patients

Activating mutations in human acute megakaryoblastic leukemia.

Acute lymphoblastic leukemia in adolescent and young adults: treat as adults or as children?

An effective modestly intensive re-induction regimen with bortezomib in relapsed or refractory paediatric acute lymphoblastic leukaemia.

Biallelic inactivation of REV7 is associated with Fanconi anemia

Biallelic inactivation of REV7 is associated with Fanconi anemia

Clinical outcome of children with newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia treated between 1995 and 2005.

Cranial polyneuropathy as the first manifestation of a severe COVID-19 in a child

Criteria for evaluating response and outcome in clinical trials for children with juvenile myelomonocytic leukemia

Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemia

High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder.

Identification of distinct molecular phenotypes in acute megakaryoblastic leukemia by gene expression profiling.

Juvenile myelomonocytic leukaemia and Noonan syndrome.

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

MicroRNA-106b~25 cluster is upregulated in relapsed MLL-rearranged pediatric acute myeloid leukemia

Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions

Nelarabine for T cell acute lymphoblastic leukemia relapsing after allogeneic hematopoietic stem cell transplantation: an opportunity to improve survival

Outcome of acute promyelocytic leukemia (APL) in children and adolescents: an analysis in two consecutive trials of the European APL Group.

Outcomes after induction failure in childhood acute lymphoblastic leukemia

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

When can real-time quantitative RT-PCR effectively define molecular relapse in acute promyelocytic leukemia patients? (Results of the French Belgian Swiss APL Group).