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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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Complementation in monocyte hybrids revealing genetic heterogeneity in chronic granulomatous disease

Nature (London), 1984-01, Vol.307 (5951), p.553-555

1984

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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

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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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

Complementation in monocyte hybrids revealing genetic heterogeneity in chronic granulomatous disease

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

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