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Rituximab therapy for childhood Evans syndrome

Haematologica (Roma), 2007-12, Vol.92 (12), p.1691-1694

2007

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An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome

Human molecular genetics, 1993-06, Vol.2 (6), p.731-735

1993

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Pearson's marrow-pancreas syndrome : a multisystem mitochondrial disorder in infancy

The Journal of clinical investigation, 1990-11, Vol.86 (5), p.1601-1608

1990

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Treatment of Familial Hemophagocytic Lymphohistiocytosis With Antithymocyte Globulins, Steroids, and Cyclosporin A

Blood, 1993-10, Vol.82 (8), p.2319-2323

1993

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Anémie hémolytique auto-immune et dysérythropoïèse révélatrices d'un déficit de l'apoptose Fas chez 3 enfants

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2006-04, Vol.13 (4), p.367-370

2006

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A human non-XLA immunodeficiency disease characterized by blockage of B cell development at an early proB cell stage

The Journal of clinical investigation, 1996-10, Vol.98 (7), p.1519-1526

1996

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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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Physical mapping by FISH of the DiGeorge critical region (DGCR) : involvement of the region in familial cases

American journal of human genetics, 1993-12, Vol.53 (6), p.1239-1249

1993

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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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Atypical X-Linked Severe Combined Immunodeficiency Due to Possible Spontaneous Reversion of the Genetic Defect in T Cells

The New England journal of medicine, 1996-11, Vol.335 (21), p.1563-1567

1996

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Major histocompatibility complex class II deficiency: Clinical manifestations, immunologic features, and outcome

The Journal of pediatrics, 1993-12, Vol.123 (6), p.921-928

1993

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Clinical, immunological, and pathological consequences of Fas-deficient conditions

The Lancet (British edition), 1996-09, Vol.348 (9029), p.719-723

1996

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A non-XLA primary deficiency causes the earliest known defect of B cell differentiation in humans: a comparison with an XLA case

Immunology letters, 1997-06, Vol.57 (1), p.93-99

1997

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Idiopathic disseminated bacillus Calmette-Guérin infection: a French national retrospective study

Pediatrics (Evanston), 1996-10, Vol.98 (4 Pt 1), p.774

1996

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Unusual T cell clones in a patient with Nijmegen breakage syndrome

Journal of medical genetics, 1992-02, Vol.29 (2), p.136-137

1992

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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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Partial albinism with immunodeficiency (Griscelli syndrome)

The Journal of pediatrics, 1994-12, Vol.125 (6), p.886-895

1994

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Auto-immune hemolytic anemia and dyserythropoïesis as the presenting signs of Fas-deficient condition in 3 children

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2006-04, Vol.13 (4), p.367-370

2006

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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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Treatment of Familial Hemophagocytic Lymphohistiocytosis With Bone Marrow Transplantation From HLA Genetically Nonidentical Donors

Blood, 1997-12, Vol.90 (12), p.4743-4748

1997

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A Primary T-Cell Immunodeficiency Associated With Defective Transmembrane Calcium Influx

Blood, 1995-02, Vol.85 (4), p.1053-1062

1995

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Adoptive Immunotherapy with Donor Allodepleted T Cells

Blood, 2005-11, Vol.106 (11), p.479-479

2005

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Dyserythropoiesis associated with a Fas‐deficient condition in childhood

British journal of haematology, 2000-02, Vol.108 (2), p.300-304

2000

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Bone marrow gene transfer in three patients with adenosine deaminase deficiency

Gene therapy, 1996-02, Vol.3 (2), p.179

1996

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Anti–B-Cell Monoclonal Antibodies in the Treatment of Severe B-Cell Lymphoproliferative Syndrome Following Bone Marrow and Organ Transplantation

The New England journal of medicine, 1991-05, Vol.324 (21), p.1451-1456

1991

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Rituximab therapy for childhood Evans syndrome

An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome

Pearson's marrow-pancreas syndrome : a multisystem mitochondrial disorder in infancy

Treatment of Familial Hemophagocytic Lymphohistiocytosis With Antithymocyte Globulins, Steroids, and Cyclosporin A

Anémie hémolytique auto-immune et dysérythropoïèse révélatrices d'un déficit de l'apoptose Fas chez 3 enfants

A human non-XLA immunodeficiency disease characterized by blockage of B cell development at an early proB cell stage

Mutations in Fas Associated with Human Lymphoproliferative Syndrome and Autoimmunity

Physical mapping by FISH of the DiGeorge critical region (DGCR) : involvement of the region in familial cases

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

Atypical X-Linked Severe Combined Immunodeficiency Due to Possible Spontaneous Reversion of the Genetic Defect in T Cells

Major histocompatibility complex class II deficiency: Clinical manifestations, immunologic features, and outcome

Clinical, immunological, and pathological consequences of Fas-deficient conditions

A non-XLA primary deficiency causes the earliest known defect of B cell differentiation in humans: a comparison with an XLA case

Idiopathic disseminated bacillus Calmette-Guérin infection: a French national retrospective study

Unusual T cell clones in a patient with Nijmegen breakage syndrome

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

Partial albinism with immunodeficiency (Griscelli syndrome)

Auto-immune hemolytic anemia and dyserythropoïesis as the presenting signs of Fas-deficient condition in 3 children

NATURALLY OCCURRING PRIMARY DEFICIENCIES OF THE IMMUNE SYSTEM

Treatment of Familial Hemophagocytic Lymphohistiocytosis With Bone Marrow Transplantation From HLA Genetically Nonidentical Donors

A Primary T-Cell Immunodeficiency Associated With Defective Transmembrane Calcium Influx

Adoptive Immunotherapy with Donor Allodepleted T Cells

Dyserythropoiesis associated with a Fas‐deficient condition in childhood

Bone marrow gene transfer in three patients with adenosine deaminase deficiency

Anti–B-Cell Monoclonal Antibodies in the Treatment of Severe B-Cell Lymphoproliferative Syndrome Following Bone Marrow and Organ Transplantation

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