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A Case of Wiskott-Aldrich Syndrome With Dual Mutations in Exon 10 of the WASP Gene: An Additional De Novo One-Base Insertion, Which Restores Frame Shift Due to an Inherent One-Base Deletion, Detected in the Major Population of the Patient's Peripheral Blood Lymphocytes

Blood, 1998-07, Vol.92 (2), p.699-701

1998

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Two-exon skipping due to a point mutation in p67-phox--deficient chronic granulomatous disease

Blood, 1996-09, Vol.88 (5), p.1841-1845

1996

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B-cell lymphoma associated with DiGeorge syndrome

European journal of pediatrics, 1999-07, Vol.158 (7), p.609-609

1999

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Bacteria-associated haemophagocytic syndrome and septic pulmonary embolism caused by Burkholderia cepacia complex in a woman with chronic granulomatous disease

Journal of medical microbiology, 2007-05, Vol.56 (5), p.702-705

2007

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Deficient expression of Bruton's tyrosine kinase in monocytes from X-linked agammaglobulinemia as evaluated by a flow cytometric analysis and its clinical application to carrier detection

Blood, 1998-01, Vol.91 (2), p.595-602

1998

Volltextzugriff (PDF)

A novel cytosolic component, p40phox, of respiratory burst oxidase associates with p67phox and is absent in patients with chronic granulomatous disease who lack p67phox

Biochemical and biophysical research communications, 1994-03, Vol.199 (3), p.1378-1387

1994

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Mutation at histidine 338 of gp91(phox) depletes FAD and affects expression of cytochrome b558 of the human NADPH oxidase

The Journal of biological chemistry, 1998-10, Vol.273 (43), p.27879

1998

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Alpha-fodrin auto-antibody in Sjögren syndrome and other auto-immune diseases in childhood

European journal of pediatrics, 2001-08, Vol.160 (8), p.520-521

2001

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Twelve cases of systemic lupus erythematosus in boys

Ryumachi. [Rheumatism], 1998-06, Vol.38 (3), p.496

1998

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Genetic studies of three Japanese patients with p22‐phox‐deficient chronic granulomatous disease: detection of a possible common mutant CYBA allele in Japan and a genotype–phenotype correlation in these patients

British journal of haematology, 2000-03, Vol.108 (3), p.511-517

2000

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Detection of antibodies to human parvovirus in erythema infectiosum (fifth disease)

Archives of disease in childhood, 1984-11, Vol.59 (11), p.1016-1019

1984

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Two-exon skipping due to a point mutation in p67-phox-deficient chronic granulomatous disease

Blood, 1996-09, Vol.88 (5), p.1841-1845

1996

Volltextzugriff (PDF)

Mutation at Histidine 338 of gp91phox Depletes FAD and Affects Expression of Cytochrome b sub(558) of the Human NADPH Oxidase

The Journal of biological chemistry, 1998-10, Vol.273 (43), p.27879-27886

1998

Volltextzugriff (PDF)

Clinical study of systemic juvenile rheumatoid arthritis (Still)

Ryumachi. [Rheumatism], 1992-04, Vol.32 (2), p.114

1992

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Detection of anti-human parvovirus IgM and IgG in erythema infectiosum

Kansenshōgaku zasshi, 1984-11, Vol.58 (11), p.1213

1984

Volltextzugriff (PDF)

Variant Streptococcus sanguis as an etiological agent of Kawasaki disease

Progress in clinical and biological research, 1987, Vol.250, p.571

1987

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A Novel Cytosolic Component, p40 phox, of Respiratory Burst Oxidase Associates with p67 phox and Is Absent in Patients with Chronic Granulomatous Disease Who Lack p67 phox

Biochemical and biophysical research communications, 1994, Vol.199 (3), p.1378-1387

1994

Volltextzugriff (PDF)

Therapeutic evaluation of combination therapy using C-425, human native immunoglobulin liquid preparation for i.v. administration, and antibiotics in severe and/or refractory infections in pediatrics

Kansenshōgaku zasshi, 1990, Vol.64 (1), p.34

1990

Volltextzugriff (PDF)

Pharyngoconjunctival fever

Ryoikibetsu shokogun shirizu, 1999 (25 Pt 3), p.148

1999

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Infectious mononucleosis

Ryoikibetsu shokogun shirizu, 1999 (25 Pt 3), p.145

1999

Volltextzugriff (PDF)

Herpangina

Ryoikibetsu shokogun shirizu, 1999 (25 Pt 3), p.151

1999

Volltextzugriff (PDF)

The Latex Agglutination Test for the Measurement of Antibodies to Group A Specific Streptococcal Polysaccharides

Pediatrics international, 1977-12, Vol.19 (2), p.28-29

Tatsuzawa, Osamu

1977

Volltextzugriff (PDF)

VARICELLA-ZOSTER VIRUS INFECTION IN CHRONIC GRANULOMATOUS DISEASE

The Pediatric infectious disease journal, 1988-11, Vol.7 (11), p.809-809

1988

Volltextzugriff (PDF)

Identification of a genetic risk factor for systemic juvenile rheumatoid arthritis in the 5′‐flanking region of the TNFα gene and HLA genes

Arthritis and rheumatism, 1999-12, Vol.42 (12), p.2577-2582

1999

Volltextzugriff (PDF)

Characteristics of juvenile dermatomyositis in Japan

Acta paediatrica Japonica. Overseas edition, 1997-04, Vol.39 (2), p.257-262

1997

Volltextzugriff (PDF)

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A Case of Wiskott-Aldrich Syndrome With Dual Mutations in Exon 10 of the WASP Gene: An Additional De Novo One-Base Insertion, Which Restores Frame Shift Due to an Inherent One-Base Deletion, Detected in the Major Population of the Patient's Peripheral Blood Lymphocytes

Two-exon skipping due to a point mutation in p67-phox--deficient chronic granulomatous disease

B-cell lymphoma associated with DiGeorge syndrome

Bacteria-associated haemophagocytic syndrome and septic pulmonary embolism caused by Burkholderia cepacia complex in a woman with chronic granulomatous disease

Deficient expression of Bruton's tyrosine kinase in monocytes from X-linked agammaglobulinemia as evaluated by a flow cytometric analysis and its clinical application to carrier detection

A novel cytosolic component, p40phox, of respiratory burst oxidase associates with p67phox and is absent in patients with chronic granulomatous disease who lack p67phox

Mutation at histidine 338 of gp91(phox) depletes FAD and affects expression of cytochrome b558 of the human NADPH oxidase

Alpha-fodrin auto-antibody in Sjögren syndrome and other auto-immune diseases in childhood

Twelve cases of systemic lupus erythematosus in boys

Genetic studies of three Japanese patients with p22‐phox‐deficient chronic granulomatous disease: detection of a possible common mutant CYBA allele in Japan and a genotype–phenotype correlation in these patients

Detection of antibodies to human parvovirus in erythema infectiosum (fifth disease)

Two-exon skipping due to a point mutation in p67-phox-deficient chronic granulomatous disease

Mutation at Histidine 338 of gp91phox Depletes FAD and Affects Expression of Cytochrome b sub(558) of the Human NADPH Oxidase

Clinical study of systemic juvenile rheumatoid arthritis (Still)

Detection of anti-human parvovirus IgM and IgG in erythema infectiosum

Variant Streptococcus sanguis as an etiological agent of Kawasaki disease

A Novel Cytosolic Component, p40 phox, of Respiratory Burst Oxidase Associates with p67 phox and Is Absent in Patients with Chronic Granulomatous Disease Who Lack p67 phox

Therapeutic evaluation of combination therapy using C-425, human native immunoglobulin liquid preparation for i.v. administration, and antibiotics in severe and/or refractory infections in pediatrics

Pharyngoconjunctival fever

Infectious mononucleosis

Herpangina

The Latex Agglutination Test for the Measurement of Antibodies to Group A Specific Streptococcal Polysaccharides

VARICELLA-ZOSTER VIRUS INFECTION IN CHRONIC GRANULOMATOUS DISEASE

Identification of a genetic risk factor for systemic juvenile rheumatoid arthritis in the 5′‐flanking region of the TNFα gene and HLA genes

Characteristics of juvenile dermatomyositis in Japan

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