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Prognostic factors for health-related quality of life in adults and children with primary antibody deficiencies receiving SCIG home therapy

Clinical immunology (Orlando, Fla.), 2008-01, Vol.126 (1), p.81-88

2008

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Efficacy and safety of home‐based subcutaneous immunoglobulin replacement therapy in paediatric patients with primary immunodeficiencies

Clinical and experimental immunology, 2011-06, Vol.164 (3), p.357-364

2011

Volltextzugriff (PDF)

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

Nature genetics, 2001-01, Vol.27 (1), p.20-21

2001

Volltextzugriff (PDF)

Common variable immunodeficiency (CVID): new genetic insight and unanswered questions

Clinical and experimental immunology, 2014-12, Vol.178 (S1), p.5-6

Ochs, H. D.

2014

Volltextzugriff (PDF)

IPEX is a unique X-linked syndrome characterized by immune dysfunction, polyendocrinopathy, enteropathy, and a variety of autoimmune phenomena

Current opinion in pediatrics, 2001-12, Vol.13 (6), p.533-538

2001

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The Wiskott-Aldrich syndrome

Journal of Allergy and Clinical Immunology, 2006-04, Vol.117 (4), p.725-738

2006

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Intensive postgrafting immune suppression combined with nonmyeloablative conditioning for transplantation of HLA-identical hematopoietic cell grafts: results of a pilot study for treatment of primary immunodeficiency disorders

Bone marrow transplantation (Basingstoke), 2007-10, Vol.40 (7), p.633-642

2007

Volltextzugriff (PDF)

Effects of administration of a single dose of a humanized monoclonal antibody to CD11a on the immunobiology and clinical activity of psoriasis

Journal of the American Academy of Dermatology, 2000-03, Vol.42 (3), p.428-435

2000

Volltextzugriff (PDF)

Immunomodulatory Effects of Mixed Hematopoietic Chimerism: Immune Tolerance in Canine Model of Lung Transplantation

American journal of transplantation, 2009-05, Vol.9 (5), p.1037-1047

2009

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Subcutaneous immunoglobulin: opportunities and outlook

Clinical and experimental immunology, 2009-12, Vol.158 (Supplement_1), p.51-59

2009

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The Wiskott-Aldrich Syndrome and X-Linked Congenital Thrombocytopenia Are Caused by Mutations of the Same Gene

Blood, 1995-11, Vol.86 (10), p.3797-3804

1995

Volltextzugriff (PDF)

Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX)

Journal of medical genetics, 2001-12, Vol.38 (12), p.874-876

2001

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The Wiskott-Aldrich syndrome

Seminars in hematology, 1998-10, Vol.35 (4), p.332

Ochs, H D

1998

Volltextzugriff (PDF)

Primary Immune Deficiency Disorders Presenting as Autoimmune Diseases: IPEX and APECED

Journal of clinical immunology, 2008-05, Vol.28 (Suppl 1), p.11-19

2008

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Absence of IgD-CD27(+) memory B cell population in X-linked hyper-IgM syndrome

The Journal of clinical investigation, 1998-08, Vol.102 (4), p.853-860

1998

Volltextzugriff (PDF)

Inhaled IFN-gamma for persistent nontuberculous mycobacterial pulmonary disease due to functional IFN-gamma deficiency

The European respiratory journal, 2004-09, Vol.24 (3), p.367-370

2004

Volltextzugriff (PDF)

The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome

Cell, 1993-01, Vol.72 (2), p.291-300

1993

Volltextzugriff (PDF)

Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination

Nature immunology, 2003-10, Vol.4 (10), p.1023-1028

2003

Volltextzugriff (PDF)

7th International Immunoglobulin Conference: Immunodeficiencies

Clinical and experimental immunology, 2014-12, Vol.178 (S1), p.3-4

2014

Volltextzugriff (PDF)

7th International Immunoglobulin Conference: Immunodeficiencies

Clinical and experimental immunology, 2014-12, Vol.178 (S1), p.21-21

2014

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B cell activation via CD40 is required for specific antibody production by antigen-stimulated human B cells

The Journal of experimental medicine, 1993-09, Vol.178 (3), p.1097-1102

1993

Volltextzugriff (PDF)

WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia

Human molecular genetics, 1995-07, Vol.4 (7), p.1127-1135

1995

Volltextzugriff (PDF)

Immunodeficiencies

Clinical and experimental immunology, 2009-12, Vol.158 (Supplement_1), p.14-22

2009

Volltextzugriff (PDF)

A high frequency of distinct ATM gene mutations in ataxia-telangiectasia

American journal of human genetics, 1996-10, Vol.59 (4), p.839-846

1996

Volltextzugriff (PDF)

The Wiskott-Aldrich syndrome

Clinical reviews in allergy & immunology, 2001-02, Vol.20 (1), p.61-86

Ochs, H D

2001

Volltextzugriff (PDF)

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Prognostic factors for health-related quality of life in adults and children with primary antibody deficiencies receiving SCIG home therapy

Efficacy and safety of home‐based subcutaneous immunoglobulin replacement therapy in paediatric patients with primary immunodeficiencies

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

Common variable immunodeficiency (CVID): new genetic insight and unanswered questions

IPEX is a unique X-linked syndrome characterized by immune dysfunction, polyendocrinopathy, enteropathy, and a variety of autoimmune phenomena

The Wiskott-Aldrich syndrome

Intensive postgrafting immune suppression combined with nonmyeloablative conditioning for transplantation of HLA-identical hematopoietic cell grafts: results of a pilot study for treatment of primary immunodeficiency disorders

Effects of administration of a single dose of a humanized monoclonal antibody to CD11a on the immunobiology and clinical activity of psoriasis

Immunomodulatory Effects of Mixed Hematopoietic Chimerism: Immune Tolerance in Canine Model of Lung Transplantation

Subcutaneous immunoglobulin: opportunities and outlook

The Wiskott-Aldrich Syndrome and X-Linked Congenital Thrombocytopenia Are Caused by Mutations of the Same Gene

Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX)

The Wiskott-Aldrich syndrome

Primary Immune Deficiency Disorders Presenting as Autoimmune Diseases: IPEX and APECED

Absence of IgD-CD27(+) memory B cell population in X-linked hyper-IgM syndrome

Inhaled IFN-gamma for persistent nontuberculous mycobacterial pulmonary disease due to functional IFN-gamma deficiency

The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome

Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination

7th International Immunoglobulin Conference: Immunodeficiencies

7th International Immunoglobulin Conference: Immunodeficiencies

B cell activation via CD40 is required for specific antibody production by antigen-stimulated human B cells

WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia

Immunodeficiencies

A high frequency of distinct ATM gene mutations in ataxia-telangiectasia

The Wiskott-Aldrich syndrome

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