Lista de obras -

Asparagine levels in the cerebrospinal fluid of children with acute lymphoblastic leukemia treated with pegylated-asparaginase in the induction phase of the AIEOP-BFM ALL 2009 study

artículo científico publicado en 2019

Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene.

artículo científico publicado en 2018

Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genes ⬇️

artículo científico publicado el 1 de octubre de 2012

Clinical impact of miR-223 expression in pediatric T-Cell lymphoblastic lymphoma.

artículo científico publicado en 2017

Co-infusion of ex vivo-expanded, parental MSCs prevents life-threatening acute GVHD, but does not reduce the risk of graft failure in pediatric patients undergoing allogeneic umbilical cord blood transplantation

artículo científico publicado en 2010

Comprehensive characterization of mesenchymal stromal cells from patients with Fanconi anaemia

artículo científico publicado en 2015

Cord blood transplantation in children with haematological malignancies ⬇️

artículo científico publicado el 1 de junio de 2010

Detection of prognostic factors in children and adolescents with Burkitt and Diffuse Large B-Cell Lymphoma treated with the AIEOP LNH-97 protocol

artículo científico publicado en 2016

Diamond-Blackfan anemia: genotype-phenotype correlations in Italian patients with RPL5 and RPL11 mutations

artículo científico publicado en 2009

Durable remissions in TCF3-HLF positive acute lymphoblastic leukemia with blinatumomab and stem cell transplantation

artículo científico publicado en 2019

Efficacy of third-party chimeric antigen receptor modified peripheral blood natural killer cells for adoptive cell therapy of B-cell precursor acute lymphoblastic leukemia

artículo científico publicado en 2019

Ex vivo expansion of mesenchymal stromal cells ⬇️

artículo científico publicado el 23 de febrero de 2011

HLA-G+3027 polymorphism is associated with tumor relapse in pediatric Hodgkin's lymphoma.

artículo científico publicado en 2017

High frequency of ribosomal protein gene deletions in Italian Diamond-Blackfan anemia patients detected by multiplex ligation-dependent probe amplification assay.

artículo científico publicado en 2012

Imatinib and Nilotinib Off-Target Effects on Human NK Cells, Monocytes, and M2 Macrophages.

artículo científico publicado en 2017

Kinetics of Circulating Plasma Cell-Free DNA in Paediatric Classical Hodgkin Lymphoma

artículo científico publicado en 2016

PACSIN2 rs2413739 influence on thiopurine pharmacokinetics: validation studies in pediatric patients

scientific article published on 03 December 2019

Primary mediastinal large B-cell lymphoma: Outcome of a series of pediatric patients treated with high-dose methotrexate and cytarabine plus anti-CD20.

artículo científico publicado en 2017

TIM-3/Gal-9 interaction induces IFNγ-dependent IDO1 expression in acute myeloid leukemia blast cells

artículo científico publicado en 2015

The combination of bortezomib with chemotherapy to treat relapsed/refractory acute lymphoblastic leukaemia of childhood.

artículo científico publicado en 2017

Treosulfan-based conditioning regimen for allogeneic haematopoietic stem cell transplantation in children with sickle cell disease

artículo científico publicado en 2015

Lista de obras de

Asparagine levels in the cerebrospinal fluid of children with acute lymphoblastic leukemia treated with pegylated-asparaginase in the induction phase of the AIEOP-BFM ALL 2009 study

Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene.

Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genes ⬇️

Clinical impact of miR-223 expression in pediatric T-Cell lymphoblastic lymphoma.

Co-infusion of ex vivo-expanded, parental MSCs prevents life-threatening acute GVHD, but does not reduce the risk of graft failure in pediatric patients undergoing allogeneic umbilical cord blood transplantation

Comprehensive characterization of mesenchymal stromal cells from patients with Fanconi anaemia

Cord blood transplantation in children with haematological malignancies ⬇️

Detection of prognostic factors in children and adolescents with Burkitt and Diffuse Large B-Cell Lymphoma treated with the AIEOP LNH-97 protocol

Diamond-Blackfan anemia: genotype-phenotype correlations in Italian patients with RPL5 and RPL11 mutations

Durable remissions in TCF3-HLF positive acute lymphoblastic leukemia with blinatumomab and stem cell transplantation

Efficacy of third-party chimeric antigen receptor modified peripheral blood natural killer cells for adoptive cell therapy of B-cell precursor acute lymphoblastic leukemia

Ex vivo expansion of mesenchymal stromal cells ⬇️

HLA-G+3027 polymorphism is associated with tumor relapse in pediatric Hodgkin's lymphoma.

High frequency of ribosomal protein gene deletions in Italian Diamond-Blackfan anemia patients detected by multiplex ligation-dependent probe amplification assay.

Imatinib and Nilotinib Off-Target Effects on Human NK Cells, Monocytes, and M2 Macrophages.

Kinetics of Circulating Plasma Cell-Free DNA in Paediatric Classical Hodgkin Lymphoma

PACSIN2 rs2413739 influence on thiopurine pharmacokinetics: validation studies in pediatric patients

Primary mediastinal large B-cell lymphoma: Outcome of a series of pediatric patients treated with high-dose methotrexate and cytarabine plus anti-CD20.

TIM-3/Gal-9 interaction induces IFNγ-dependent IDO1 expression in acute myeloid leukemia blast cells

The combination of bortezomib with chemotherapy to treat relapsed/refractory acute lymphoblastic leukaemia of childhood.

Treosulfan-based conditioning regimen for allogeneic haematopoietic stem cell transplantation in children with sickle cell disease