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Haematopoietic stem cell transplantation for refractory Langerhans cell histiocytosis: outcome by intensity of conditioning

British journal of haematology, 2015-06, Vol.169 (5), p.711-718

2015

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Long-term results of the Italian Association of Pediatric Hematology and Oncology (AIEOP) Studies 82, 87, 88, 91 and 95 for childhood acute lymphoblastic leukemia

Leukemia, 2010-02, Vol.24 (2), p.255-264

2010

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Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21

Blood, 2003-08, Vol.102 (3), p.981-986

2003

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Prenatal origin of acute lymphoblastic leukaemia in children

The Lancet (British edition), 1999-10, Vol.354 (9189), p.1499-1503

1999

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Outcome of treatment in childhood acute lymphoblastic leukaemia with rearrangements of the 11q23 chromosomal region

The Lancet (British edition), 2002-06, Vol.359 (9321), p.1909-1915

2002

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Clinical heterogeneity in childhood acute lymphoblastic leukemia with 11q23 rearrangements

Leukemia, 2003-04, Vol.17 (4), p.700-706

2003

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Contribution of the TATA-box genotype (Gilbert syndrome) to serum bilirubin concentrations in the Italian population

Clinical chemistry (Baltimore, Md.), 1999-06, Vol.45 (6), p.897-898

1999

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Immunogenotype Changes Prevail in Relapses of Young Children with TEL-AML1-Positive Acute Lymphoblastic Leukemia and Derive Mainly from Clonal Selection

Clinical cancer research, 2005-11, Vol.11 (21), p.7720-7727

2005

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Expression of CD58 in normal, regenerating and leukemic bone marrow B cells: implications for the detection of minimal residual disease in acute lymphocytic leukemia

Haematologica (Roma), 2003-11, Vol.88 (11), p.1245

2003

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Immunophenotype of adult and childhood acute promyelocytic leukaemia: correlation with morphology, type of PML gene breakpoint and clinical outcome. A cooperative Italian study on 196 cases

British journal of haematology, 1998-09, Vol.102 (4), p.1035-1041

1998

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Autologous purified peripheral blood SCT in childhood low-risk relapsed ALL

Bone marrow transplantation (Basingstoke), 2011-02, Vol.46 (2), p.217-226

2011

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Gemtuzumab ozogamicin in pediatric CD33-positive acute lymphoblastic leukemia: first clinical experiences and relation with cellular sensitivity to single agent calicheamicin

Leukemia, 2003-02, Vol.17 (2), p.468-470

2003

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Development of a quantitative-PCR method for specific FLT3 ITD monitoring in acute myeloid leukemia

Leukemia, 2004-08, Vol.18 (8), p.1441-1444

2004

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No prognostic effect of additional chromosomal abnormalities in children with acute lymphoblastic leukemia and 11q23 abnormalities

Leukemia, 2005-04, Vol.19 (4), p.557-563

2005

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t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia

Genes chromosomes & cancer, 2000-12, Vol.29 (4), p.325-332

2000

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Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia

Genes chromosomes & cancer, 2003-10, Vol.38 (2), p.191-200

2003

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Reconstitution of lymphocyte subpopulations in children with inherited metabolic storage diseases after haematopoietic cell transplantation

British journal of haematology, 2005-07, Vol.130 (2), p.249-255

2005

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Characterization of CD34+, CD13+, CD33- cells, a rare subset of immature human hematopoietic cells

Haematologica (Roma), 2002-04, Vol.87 (4), p.347

2002

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ALL-1 gene at chromosome 11q23 is consistently altered in acute leukemia of early infancy

Blood, 1993-07, Vol.82 (2), p.544-546

1993

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ALL-1 gene rearrangements in acute myeloid leukemia: association with M4-M5 French-American-British classification subtypes and young age

Cancer research (Chicago, Ill.), 1995-04, Vol.55 (8), p.1625-1628

1995

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Clinical relevance of residual disease monitoring by polymerase chain reaction in patients with ALL‐1/AF‐4 positive‐acute lymphoblastic leukaemia

British journal of haematology, 1996-03, Vol.92 (3), p.659-664

1996

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Biodemography and genetics of the Berba of Benin

American journal of physical anthropology, 1996-04, Vol.99 (4), p.519-535

1996

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Multigenetic lesions in infant acute leukaemias: correlations with ALL‐1 gene status

British journal of haematology, 1997-02, Vol.96 (2), p.308-313

1997

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Minimal residual disease in childhood acute lymphoblastic leukemia: analysis of patients in continuous complete remission or with consecutive relapse

Leukemia, 1992-04, Vol.6 (4), p.282-288

1992

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Time point-dependent concordance of flow cytometry and real-time quantitative polymerase chain reaction for minimal residual disease detection in childhood acute lymphoblastic leukemia

Haematopoietic stem cell transplantation for refractory Langerhans cell histiocytosis: outcome by intensity of conditioning

Long-term results of the Italian Association of Pediatric Hematology and Oncology (AIEOP) Studies 82, 87, 88, 91 and 95 for childhood acute lymphoblastic leukemia

Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21

Prenatal origin of acute lymphoblastic leukaemia in children

Outcome of treatment in childhood acute lymphoblastic leukaemia with rearrangements of the 11q23 chromosomal region

Clinical heterogeneity in childhood acute lymphoblastic leukemia with 11q23 rearrangements

Contribution of the TATA-box genotype (Gilbert syndrome) to serum bilirubin concentrations in the Italian population

Immunogenotype Changes Prevail in Relapses of Young Children with TEL-AML1-Positive Acute Lymphoblastic Leukemia and Derive Mainly from Clonal Selection

Expression of CD58 in normal, regenerating and leukemic bone marrow B cells: implications for the detection of minimal residual disease in acute lymphocytic leukemia

Immunophenotype of adult and childhood acute promyelocytic leukaemia: correlation with morphology, type of PML gene breakpoint and clinical outcome. A cooperative Italian study on 196 cases

Autologous purified peripheral blood SCT in childhood low-risk relapsed ALL

Gemtuzumab ozogamicin in pediatric CD33-positive acute lymphoblastic leukemia: first clinical experiences and relation with cellular sensitivity to single agent calicheamicin

Development of a quantitative-PCR method for specific FLT3 ITD monitoring in acute myeloid leukemia

No prognostic effect of additional chromosomal abnormalities in children with acute lymphoblastic leukemia and 11q23 abnormalities

t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia

Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia

Reconstitution of lymphocyte subpopulations in children with inherited metabolic storage diseases after haematopoietic cell transplantation

Characterization of CD34+, CD13+, CD33- cells, a rare subset of immature human hematopoietic cells

ALL-1 gene at chromosome 11q23 is consistently altered in acute leukemia of early infancy

ALL-1 gene rearrangements in acute myeloid leukemia: association with M4-M5 French-American-British classification subtypes and young age

Clinical relevance of residual disease monitoring by polymerase chain reaction in patients with ALL‐1/AF‐4 positive‐acute lymphoblastic leukaemia

Biodemography and genetics of the Berba of Benin

Multigenetic lesions in infant acute leukaemias: correlations with ALL‐1 gene status

Minimal residual disease in childhood acute lymphoblastic leukemia: analysis of patients in continuous complete remission or with consecutive relapse

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