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Mutations in NALP12 cause hereditary periodic fever syndromes

Proceedings of the National Academy of Sciences - PNAS, 2008-02, Vol.105 (5), p.1614-1619

2008

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Abatacept is useful in autoimmune cytopenia with immunopathologic manifestations caused by CTLA-4 defects

Blood, 2022-01, Vol.139 (2), p.300-304

2022

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Lymphocyte-Predominant Hodgkin’s Lymphoma in Children: Therapeutic Abstention After Initial Lymph Node Resection—A Study of the French Society of Pediatric Oncology

Journal of clinical oncology, 2003-08, Vol.21 (15), p.2948-2952

2003

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Age and high-dose methotrexate are associated to clinical acute encephalopathy in FRALLE 93 trial for acute lymphoblastic leukemia in children

Leukemia, 2007-02, Vol.21 (2), p.238-247

2007

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Localized Childhood Hodgkin’s Disease: Response-Adapted Chemotherapy With Etoposide, Bleomycin, Vinblastine, and Prednisone Before Low-Dose Radiation Therapy—Results of the French Society of Pediatric Oncology Study MDH90

Journal of clinical oncology, 2000-04, Vol.18 (7), p.1500-1507

2000

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

Oncogene, 2015-01, Vol.34 (5), p.631-638

2015

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SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype

Journal of medical genetics, 2009-07, Vol.46 (7), p.425-430

2009

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Multi-centre pilot study of 2-chlorodeoxyadenosine and cytosine arabinoside combined chemotherapy in refractory Langerhans cell histiocytosis with haematological dysfunction

European journal of cancer (1990), 2005-11, Vol.41 (17), p.2682-2689

2005

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Combined therapy in children and adolescents with classical Hodgkin's lymphoma: A report from the SFCE on MDH-03 national guidelines

Pediatric hematology and oncology, 2016-11, Vol.33 (7-8), p.423-437

2016

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Use of Recombinant Human Granulocyte Colony-Stimulating Factor to Increase Chemotherapy Dose-Intensity: A Randomized Trial in Very High-Risk Childhood Acute Lymphoblastic Leukemia

Journal of clinical oncology, 2000-04, Vol.18 (7), p.1517-1524

2000

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Extensive mutational status of genes and clinical outcome in pediatric acute myeloid leukemia

Leukemia, 2010-01, Vol.24 (1), p.205-209

2010

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Detection of Mycoplasma pneumoniae in clinical samples from pediatric patients by polymerase chain reaction

Journal of Clinical Microbiology, 1992-10, Vol.30 (10), p.2638-2643

1992

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Hodgkin disease and autoimmunity in children: 11 case reports

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2011-04, Vol.18 (4), p.376-382

2011

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High WT1 Expression After Induction Therapy Predicts High Risk of Relapse and Death in Pediatric Acute Myeloid Leukemia

Journal of clinical oncology, 2006-04, Vol.24 (10), p.1507-1515

2006

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NUP214-ABL1 amplification in t(5;14) HOX11L2-positive ALL present with several forms and may have a prognostic significance

Leukemia, 2005-03, Vol.19 (3), p.468-470

2005

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

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2010-12, Vol.17 (12), p.1637-1644

2010

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Increased Risk of Systemic Relapses Associated With Bone Marrow Micrometastasis and Circulating Tumor Cells in Localized Ewing Tumor

Journal of clinical oncology, 2003-01, Vol.21 (1), p.85-91

2003

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Treatment of childhood autoimmune haemolytic anaemia with rituximab

The Lancet (British edition), 2001-11, Vol.358 (9292), p.1511-1513

2001

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Long term follow up of 93 families with myeloproliferative neoplasms: life expectancy and implications of JAK2V617F in the occurrence of complications

Blood cells, molecules, & diseases, 2012-10, Vol.49 (3-4), p.170-176

2012

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Analysis of TCR, pTα, and RAG-1 in T-acute lymphoblastic leukemias improves understanding of early human T-lymphoid lineage commitment

Blood, 2003-04, Vol.101 (7), p.2693-2703

2003

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Impact of genotype on survival of children with T-cell acute lymphoblastic leukemia treated according to the French protocol FRALLE-93: the effect of TLX3/HOX11L2 gene expression on outcome

Haematologica (Roma), 2008-11, Vol.93 (11), p.1658-1665

2008

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HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis

Blood, 2002-08, Vol.100 (3), p.991-997

2002

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In a novel form of IFN-gamma receptor 1 deficiency, cell surface receptors fail to bind IFN-gamma

The Journal of clinical investigation, 2000-05, Vol.105 (10), p.1429-1436

2000

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Allogeneic bone marrow transplantation vs aggressive post-remission chemotherapy for children with acute myeloid leukemia in first complete remission. A prospective study from the French Society of Pediatric Hematology and Immunology (SHIP)

Bone marrow transplantation (Basingstoke), 1996-02, Vol.17 (2), p.191-196

1996

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Mutations in NALP12 cause hereditary periodic fever syndromes

Abatacept is useful in autoimmune cytopenia with immunopathologic manifestations caused by CTLA-4 defects

Lymphocyte-Predominant Hodgkin’s Lymphoma in Children: Therapeutic Abstention After Initial Lymph Node Resection—A Study of the French Society of Pediatric Oncology

Age and high-dose methotrexate are associated to clinical acute encephalopathy in FRALLE 93 trial for acute lymphoblastic leukemia in children

Localized Childhood Hodgkin’s Disease: Response-Adapted Chemotherapy With Etoposide, Bleomycin, Vinblastine, and Prednisone Before Low-Dose Radiation Therapy—Results of the French Society of Pediatric Oncology Study MDH90

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

SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype

Multi-centre pilot study of 2-chlorodeoxyadenosine and cytosine arabinoside combined chemotherapy in refractory Langerhans cell histiocytosis with haematological dysfunction

Combined therapy in children and adolescents with classical Hodgkin's lymphoma: A report from the SFCE on MDH-03 national guidelines

Use of Recombinant Human Granulocyte Colony-Stimulating Factor to Increase Chemotherapy Dose-Intensity: A Randomized Trial in Very High-Risk Childhood Acute Lymphoblastic Leukemia

Extensive mutational status of genes and clinical outcome in pediatric acute myeloid leukemia

Detection of Mycoplasma pneumoniae in clinical samples from pediatric patients by polymerase chain reaction

Hodgkin disease and autoimmunity in children: 11 case reports

High WT1 Expression After Induction Therapy Predicts High Risk of Relapse and Death in Pediatric Acute Myeloid Leukemia

NUP214-ABL1 amplification in t(5;14) HOX11L2-positive ALL present with several forms and may have a prognostic significance

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

Increased Risk of Systemic Relapses Associated With Bone Marrow Micrometastasis and Circulating Tumor Cells in Localized Ewing Tumor

Treatment of childhood autoimmune haemolytic anaemia with rituximab

Long term follow up of 93 families with myeloproliferative neoplasms: life expectancy and implications of JAK2V617F in the occurrence of complications

Analysis of TCR, pTα, and RAG-1 in T-acute lymphoblastic leukemias improves understanding of early human T-lymphoid lineage commitment

Impact of genotype on survival of children with T-cell acute lymphoblastic leukemia treated according to the French protocol FRALLE-93: the effect of TLX3/HOX11L2 gene expression on outcome

HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis

In a novel form of IFN-gamma receptor 1 deficiency, cell surface receptors fail to bind IFN-gamma

Allogeneic bone marrow transplantation vs aggressive post-remission chemotherapy for children with acute myeloid leukemia in first complete remission. A prospective study from the French Society of Pediatric Hematology and Immunology (SHIP)

Impact of age, leukocyte count and day 21-bone marrow response to chemotherapy on the long-term outcome of children with philadelphia chromosome-positive acute lymphoblastic leukemia in the pre-imatinib era: results of the FRALLE 93 study

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