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Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va gene

Nature genetics, 1997-07, Vol.16 (3), p.289-292

1997

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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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Infusion of Fcγ fragments for treatment of children with acute immune thrombocytopenic purpura

The Lancet (British edition), 1993-10, Vol.342 (8877), p.945-949

1993

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Estimated Timing of Mother-to-Child Human Immunodeficiency Virus Type 1 (HIV-1) Transmission by Use of a Markov Model

American journal of epidemiology, 1995-12, Vol.142 (12), p.1330-1337

1995

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Autosomal recessive osteopetrosis: variability of findings at diagnosis and during the natural course

Pediatrics (Evanston), 1994-02, Vol.93 (2), p.247-253

1994

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Incidence, severity, and prevention of infections in chronic granulomatous disease

The Journal of pediatrics, 1989-04, Vol.114 (4), p.555-560

1989

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Bone marrow transplantation in 26 patients with Wiskott-Aldrich syndrome from a single center

The Journal of pediatrics, 1996-08, Vol.129 (2), p.238-244

1996

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Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families

British Journal of Cancer, 1999-06, Vol.80 (7), p.1042-1045

1999

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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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Neutropénies constitutionnelles et acquises de l'enfant

Archives de pédiatrie (Paris), 1994, Vol.1 (10), p.925-935

1994

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Treatment of Chediak-Higashi Syndrome by Allogenic Bone Marrow Transplantation: Report of 10 Cases

Blood, 1995-06, Vol.85 (11), p.3328-3333

1995

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The Use of Viral Culture and p24 Antigen Testing to Diagnose Human Immunodeficiency Virus Infection in Neonates

The New England journal of medicine, 1992-10, Vol.327 (17), p.1192-1197

1992

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European experience of bone-marrow transplantation for severe combined immunodeficiency

The Lancet (British edition), 1990-10, Vol.336 (8719), p.850-854

1990

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Bone Marrow Transplantation in Major Histocompatibility Complex Class II Deficiency: A Single-Center Study of 19 Patients

Blood, 1995-01, Vol.85 (2), p.580-587

1995

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Treatment of Hemophagocytic Lymphohistiocytosis With Chemotherapy and Bone Marrow Transplantation: A Single-Center Study of 22 Cases

Blood, 1991-07, Vol.78 (1), p.51-54

1991

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Manifestations cutanées révélatrices d'un lymphome T γδ chez une enfant de 13 ans

Annales de dermatologie et de vénéréologie, 1993, Vol.120 (11), p.792-793

1993

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Thymic abnormalities in fetuses aborted from human immunodeficiency virus type 1 seropositive women

Pediatrics (Evanston), 1992-02, Vol.89 (2), p.297-301

1992

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Congenital immunodeficiency with a regulatory defect in MHC class II gene expression lacks a specific HLA-DR promoter binding protein, RF-X

Cell, 1988-06, Vol.53 (6), p.897-906

1988

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DETECTION OF HTV1 DNA IN INFANTS AND CHILDREN BY MEANS OF THE POLYMERASE CHAIN REACTION

The Lancet (British edition), 1988-09, Vol.332 (8610), p.538-541

1988

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Les enfants atteints de déficit immunitaire confinés en bulle et leur famille

Neuropsychiatrie de l'enfance et de l'adolescence, 1985, Vol.33 (10), p.427-434

1985

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Growth and growth hormone secretion after bone marrow transplantation

Archives of disease in childhood, 1993-04, Vol.68 (4), p.458-463

1993

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B cell immunodeficiency, distal limb abnormalities, and urogenital malformations in a three generation family: a novel autosomal dominant syndrome?

Journal of medical genetics, 2001-07, Vol.38 (7), p.488-492

2001

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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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Intractable infant diarrhea associated with phenotypic abnormalities and immunodeficiency

The Journal of pediatrics, 1994-07, Vol.125 (1), p.36-42

1994

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Treatment of Omenn syndrome by bone marrow transplantation

The Journal of pediatrics, 1995-07, Vol.127 (1), p.76-81

1995

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Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va gene

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

Infusion of Fcγ fragments for treatment of children with acute immune thrombocytopenic purpura

Estimated Timing of Mother-to-Child Human Immunodeficiency Virus Type 1 (HIV-1) Transmission by Use of a Markov Model

Autosomal recessive osteopetrosis: variability of findings at diagnosis and during the natural course

Incidence, severity, and prevention of infections in chronic granulomatous disease

Bone marrow transplantation in 26 patients with Wiskott-Aldrich syndrome from a single center

Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families

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

Neutropénies constitutionnelles et acquises de l'enfant

Treatment of Chediak-Higashi Syndrome by Allogenic Bone Marrow Transplantation: Report of 10 Cases

The Use of Viral Culture and p24 Antigen Testing to Diagnose Human Immunodeficiency Virus Infection in Neonates

European experience of bone-marrow transplantation for severe combined immunodeficiency

Bone Marrow Transplantation in Major Histocompatibility Complex Class II Deficiency: A Single-Center Study of 19 Patients

Treatment of Hemophagocytic Lymphohistiocytosis With Chemotherapy and Bone Marrow Transplantation: A Single-Center Study of 22 Cases

Manifestations cutanées révélatrices d'un lymphome T γδ chez une enfant de 13 ans

Thymic abnormalities in fetuses aborted from human immunodeficiency virus type 1 seropositive women

Congenital immunodeficiency with a regulatory defect in MHC class II gene expression lacks a specific HLA-DR promoter binding protein, RF-X

DETECTION OF HTV1 DNA IN INFANTS AND CHILDREN BY MEANS OF THE POLYMERASE CHAIN REACTION

Les enfants atteints de déficit immunitaire confinés en bulle et leur famille

Growth and growth hormone secretion after bone marrow transplantation

B cell immunodeficiency, distal limb abnormalities, and urogenital malformations in a three generation family: a novel autosomal dominant syndrome?

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

Intractable infant diarrhea associated with phenotypic abnormalities and immunodeficiency

Treatment of Omenn syndrome by bone marrow transplantation

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