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Chronic granulomatous disease: the European experience

PloS one, 2009-04, Vol.4 (4), p.e5234-e5234

2009

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The effect of two different dosages of intravenous immunoglobulin on the incidence of recurrent infections in patients with primary hypogammaglobulinemia. A randomized, double-blind, multicenter crossover trial

Annals of internal medicine, 2001-08, Vol.135 (3), p.165

2001

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Genetic analysis of patients with leukocyte adhesion deficiency: Genomic sequencing reveals otherwise undetectable mutations

Experimental hematology, 2002-03, Vol.30 (3), p.252-261

2002

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Clinical and laboratory work-up of patients with neutrophil shortage or dysfunction

Journal of immunological methods, 1999-12, Vol.232 (1), p.211-229

1999

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Mutations in the X-Linked and Autosomal Recessive Forms of Chronic Granulomatous Disease

Blood, 1996-03, Vol.87 (5), p.1663-1681

1996

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Effect of interferon-gamma, in vitro and in vivo, on mRNA levels of phagocyte oxidase components

Journal of leukocyte biology, 1996-12, Vol.60 (6), p.716-720

1996

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Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease

Blood, 1996-03, Vol.87 (5), p.1663-1681

1996

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Fc gamma receptor IIa (CD32) polymorphism in fulminant meningococcal septic shock in children

The Journal of infectious diseases, 1994-10, Vol.170 (4), p.848

1994

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A missense mutation in the heavy subunit of γ-glutamylcysteine synthetase gene causes hemolytic anemia

Blood, 2000-04, Vol.95 (7), p.2193-2197

2000

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Intracellular Reactions in Single Human Granulocytes upon Phorbol Myristate Acetate Activation using Confocal Raman Microspectroscopy

Biophysical journal, 2000-05, Vol.78 (5), p.2606-2613

2000

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Phagocytosis of Staphylococcus aureus and Haemophilus influenzae type B opsonized with polyclonal human IgG1 and IgG2 antibodies. Functional hFc gamma RIIa polymorphism to IgG2

The Journal of immunology (1950), 1993-08, Vol.151 (3), p.1463-1472

1993

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A point mutation in gp91-phox of cytochrome b558 of the human NADPH oxidase leading to defective translocation of the cytosolic proteins p47-phox and p67-phox

The Journal of clinical investigation, 1994-05, Vol.93 (5), p.2120-2126

1994

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Point Mutations in the β-Subunit of Cytochrome b558 Leading to X-Linked Chronic Granulomatous Disease

Blood, 1991-06, Vol.77 (11), p.2482-2487

1991

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Colorectal cancer in patients with X-linked agammaglobulinaemia

The Lancet (British edition), 1993-06, Vol.341 (8858), p.1439-1440

1993

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Characterization of Two Monoclonal Antibodies Against Cytochrome b558 of Human Neutrophils

Blood, 1989-05, Vol.73 (6), p.1686-1694

1989

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Genetic analysis of patients with leukocyte adhesion deficiency

Experimental hematology, 2002-03, Vol.30 (3), p.252-261

2002

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A Single Dose of Granulocyte-Macrophage Colony-Stimulating Factor Induces Systemic Interleukin-8 Release and Neutrophil Activation in Healthy Volunteers

Blood, 1996-06, Vol.87 (12), p.5305-5313

1996

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The use of rh‐G‐CSF in chronic autoimmune neutropenia: reversal of autoimmune phenomena, a case history

British journal of haematology, 1996-09, Vol.94 (3), p.464-469

1996

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Cytochrome b558-negative, autosomal recessive chronic granulomatous disease : two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox)

American journal of human genetics, 1992-11, Vol.51 (5), p.1127-1135

1992

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Splice site mutations are a common cause of X-linked chronic granulomatous disease

Blood, 1992-09, Vol.80 (6), p.1553-1558

1992

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Chronic granulomatous disease with partial deficiency of cytochrome b558 and incomplete respiratory burst: variants of the X-linked, cytochrome b558-negative form of the disease

Journal of leukocyte biology, 1992-02, Vol.51 (2), p.164-171

1992

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Discoid lupus erythematosus-like skin changes in patients with autosomal recessive chronic granulomatous disease

Archives of dermatology (1960), 1990-12, Vol.126 (12), p.1656

1990

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The use of rhaGaCSF in chronic autoimmune neutropenia: reversal of autoimmune phenomena, a case history

British journal of haematology, 1996-09, Vol.94 (3), p.464-469

1996

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Continuous cell activation is necessary for stable interaction of complement receptor type 3 with its counter‐structure in the aggregation response of human neutrophils

European journal of immunology, 1990-03, Vol.20 (3), p.501-508

1990

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Chronic granulomatous disease: the European experience

The effect of two different dosages of intravenous immunoglobulin on the incidence of recurrent infections in patients with primary hypogammaglobulinemia. A randomized, double-blind, multicenter crossover trial

Genetic analysis of patients with leukocyte adhesion deficiency: Genomic sequencing reveals otherwise undetectable mutations

Clinical and laboratory work-up of patients with neutrophil shortage or dysfunction

Mutations in the X-Linked and Autosomal Recessive Forms of Chronic Granulomatous Disease

Effect of interferon-gamma, in vitro and in vivo, on mRNA levels of phagocyte oxidase components

Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease

Molecular Basis and Enzymatic Properties of Glucose 6-Phosphate Dehydrogenase Volendam, Leading to Chronic Nonspherocytic Anemia, Granulocyte Dysfunction, and Increased Susceptibility to Infections

Fc gamma receptor IIa (CD32) polymorphism in fulminant meningococcal septic shock in children

A missense mutation in the heavy subunit of γ-glutamylcysteine synthetase gene causes hemolytic anemia

Intracellular Reactions in Single Human Granulocytes upon Phorbol Myristate Acetate Activation using Confocal Raman Microspectroscopy

Phagocytosis of Staphylococcus aureus and Haemophilus influenzae type B opsonized with polyclonal human IgG1 and IgG2 antibodies. Functional hFc gamma RIIa polymorphism to IgG2

A point mutation in gp91-phox of cytochrome b558 of the human NADPH oxidase leading to defective translocation of the cytosolic proteins p47-phox and p67-phox

Point Mutations in the β-Subunit of Cytochrome b558 Leading to X-Linked Chronic Granulomatous Disease

Colorectal cancer in patients with X-linked agammaglobulinaemia

Characterization of Two Monoclonal Antibodies Against Cytochrome b558 of Human Neutrophils

Genetic analysis of patients with leukocyte adhesion deficiency

A Single Dose of Granulocyte-Macrophage Colony-Stimulating Factor Induces Systemic Interleukin-8 Release and Neutrophil Activation in Healthy Volunteers

The use of rh‐G‐CSF in chronic autoimmune neutropenia: reversal of autoimmune phenomena, a case history

Cytochrome b558-negative, autosomal recessive chronic granulomatous disease : two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox)

Splice site mutations are a common cause of X-linked chronic granulomatous disease

Chronic granulomatous disease with partial deficiency of cytochrome b558 and incomplete respiratory burst: variants of the X-linked, cytochrome b558-negative form of the disease

Discoid lupus erythematosus-like skin changes in patients with autosomal recessive chronic granulomatous disease

The use of rhaGaCSF in chronic autoimmune neutropenia: reversal of autoimmune phenomena, a case history

Continuous cell activation is necessary for stable interaction of complement receptor type 3 with its counter‐structure in the aggregation response of human neutrophils

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