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Autoimmune lymphoproliferative syndromes: genetic defects of apoptosis pathways

Cell death and differentiation, 2003-01, Vol.10 (1), p.124-133

2003

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Reconstitution of maturating and regulatory lymphocyte subsets after cord blood and BMT in children

Bone marrow transplantation (Basingstoke), 2013-03, Vol.48 (3), p.376-382

2013

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LMO2-Associated Clonal T Cell Proliferation in Two Patients after Gene Therapy for SCID-X1

Science (American Association for the Advancement of Science), 2003-10, Vol.302 (5644), p.415-419

2003

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Comment explorer un déficit immunitaire?

Archives de pédiatrie (Paris), 2003-09, Vol.10, p.s510-s512

Le Deist, F

2003

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High prevalence of primary immune deficiencies in children with autoimmune disorders

Clinical and experimental rheumatology, 2011-01, Vol.29 (1), p.125

2011

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Impact of HLA matching on outcome of hematopoietic stem cell transplantation in children with inherited diseases: a single-center comparative analysis of genoidentical, haploidentical or unrelated donors

Bone marrow transplantation (Basingstoke), 2004-06, Vol.33 (11), p.1089-1095

2004

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Acceptability Conditions for Telemonitoring Gerontechnology in the Elderly

Ingénierie et recherche biomédicale, 2016-11, Vol.37 (5-6), p.284-288

2016

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CD40-CD40L Independent Ig Gene Hypermutation Suggests a Second B Cell Diversification Pathway in Humans

Proceedings of the National Academy of Sciences - PNAS, 2001-01, Vol.98 (3), p.1166-1170

2001

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Severe combined immunodeficiency: A retrospective single-center study of clinical presentation and outcome in 117 patients

The Journal of pediatrics, 1993-10, Vol.123 (4), p.564-572

1993

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Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B–severe combined immune deficiency or Omenn syndrome

Blood, 2001-05, Vol.97 (9), p.2772-2776

2001

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Inactivation of the Fas gene by Alu insertion: retrotransposition in an intron causing splicing variation and autoimmune lymphoproliferative syndrome

Genes and immunity, 2002-10, Vol.3 (S1), p.S66-S70

2002

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NATURALLY OCCURRING PRIMARY DEFICIENCIES OF THE IMMUNE SYSTEM

Annual review of immunology, 1997-01, Vol.15 (1), p.93-124

1997

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Coombs’ negative haemolytic anaemia as a first manifestation of autoimmune lymphoproliferative disease

British journal of haematology, 2005-05, Vol.129 (3), p.442-443

2005

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Epidemiology of autoimmune haemolytic anemia in children: French data

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2006-06, Vol.13 (6), p.511-514

2006

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Gene therapy of severe combined immunodeficiencies

The journal of gene medicine, 2001-05, Vol.3 (3), p.201-206

2001

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Mutation in the Class II trans-Activator Leading to a Mild Immunodeficiency

The Journal of immunology (1950), 2001-08, Vol.167 (3), p.1787-1794

2001

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Mutations in Fas Associated with Human Lymphoproliferative Syndrome and Autoimmunity

Science (American Association for the Advancement of Science), 1995-06, Vol.268 (5215), p.1347-1349

1995

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SIAH-1 inhibits cell growth by altering the mitotic process

Oncogene, 1999-11, Vol.18 (50), p.7101-7109

1999

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The calcium current activated by T cell receptor and store depletion in human lymphocytes is absent in a primary immunodeficiency

The Journal of biological chemistry, 1994-12, Vol.269 (51), p.32327-32335

1994

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Reduction of Graft Failure by a Monoclonal Antibody (Anti-LFA-1 CD11a) After HLA Nonidentical Bone Marrow Transplantation in Children With Immunodeficiencies, Osteopetrosis, and Fanconi’s Anemia: A European Group for Immunodeficiency/European Group for Bone Marrow Transplantation Report

Blood, 1991-01, Vol.77 (2), p.249-256

1991

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Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 Disease

Science (American Association for the Advancement of Science), 2000-04, Vol.288 (5466), p.669-672

2000

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Cernunnos, a Novel Nonhomologous End-Joining Factor, Is Mutated in Human Immunodeficiency with Microcephaly

Cell, 2006-01, Vol.124 (2), p.287-299

2006

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A Serious Adverse Event after Successful Gene Therapy for X-Linked Severe Combined Immunodeficiency

The New England journal of medicine, 2003-01, Vol.348 (3), p.255-256

2003

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Cytomegalovirus infection in infants with autoimmune lymphoproliferative syndrome (ALPS)

Clinical and experimental immunology, 2000-08, Vol.121 (2), p.353-357

2000

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Mutations in the phosphatidylinositol glycan C (PIGC) gene are associated with epilepsy and intellectual disability

Journal of medical genetics, 2017-03, Vol.54 (3), p.196-201

2017

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Autoimmune lymphoproliferative syndromes: genetic defects of apoptosis pathways

Reconstitution of maturating and regulatory lymphocyte subsets after cord blood and BMT in children

LMO2-Associated Clonal T Cell Proliferation in Two Patients after Gene Therapy for SCID-X1

Comment explorer un déficit immunitaire?

High prevalence of primary immune deficiencies in children with autoimmune disorders

Impact of HLA matching on outcome of hematopoietic stem cell transplantation in children with inherited diseases: a single-center comparative analysis of genoidentical, haploidentical or unrelated donors

Acceptability Conditions for Telemonitoring Gerontechnology in the Elderly

CD40-CD40L Independent Ig Gene Hypermutation Suggests a Second B Cell Diversification Pathway in Humans

Severe combined immunodeficiency: A retrospective single-center study of clinical presentation and outcome in 117 patients

Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B–severe combined immune deficiency or Omenn syndrome

Inactivation of the Fas gene by Alu insertion: retrotransposition in an intron causing splicing variation and autoimmune lymphoproliferative syndrome

NATURALLY OCCURRING PRIMARY DEFICIENCIES OF THE IMMUNE SYSTEM

Coombs’ negative haemolytic anaemia as a first manifestation of autoimmune lymphoproliferative disease

Epidemiology of autoimmune haemolytic anemia in children: French data

Gene therapy of severe combined immunodeficiencies

Mutation in the Class II trans-Activator Leading to a Mild Immunodeficiency

Mutations in Fas Associated with Human Lymphoproliferative Syndrome and Autoimmunity

SIAH-1 inhibits cell growth by altering the mitotic process

The calcium current activated by T cell receptor and store depletion in human lymphocytes is absent in a primary immunodeficiency

Reduction of Graft Failure by a Monoclonal Antibody (Anti-LFA-1 CD11a) After HLA Nonidentical Bone Marrow Transplantation in Children With Immunodeficiencies, Osteopetrosis, and Fanconi’s Anemia: A European Group for Immunodeficiency/European Group for Bone Marrow Transplantation Report

Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 Disease

Cernunnos, a Novel Nonhomologous End-Joining Factor, Is Mutated in Human Immunodeficiency with Microcephaly

A Serious Adverse Event after Successful Gene Therapy for X-Linked Severe Combined Immunodeficiency

Cytomegalovirus infection in infants with autoimmune lymphoproliferative syndrome (ALPS)

Mutations in the phosphatidylinositol glycan C (PIGC) gene are associated with epilepsy and intellectual disability

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