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1008 THEORETICAL AND BIOLOGICAL CONSIDERATIONS IN SUCCESSFUL MISMATCHED BONE MARROW TRANSPLANTATION

Pediatric research, 1985-04, Vol.19 (4), p.278-278A

1985

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1010 LABORATORY FINDINGS IN VARIOUS CONGENITAL IMMUNODEFICIENCIES

Pediatric research, 1985-04, Vol.19 (4), p.279-279A

1985

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105 - Infectious Complications of Complement Deficiencies

Principles and Practice of Pediatric Infectious Diseases, 2012, p.615-619.e2

Fourth Edition, 2012

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988 INDUCTION OF COMPLEMENT-MEDIATED DESTRUCTION OF HOST CELLS BY BACTERIAL LIPOTEICHOIC ACID

Pediatric research, 1985-04, Vol.19 (4), p.275-275A

1985

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The ability of bacteria to activate the terminal complement components in serum of patients with cystic fibrosis

The Journal of pediatrics, 1978-09, Vol.93 (3), p.530-531

1978

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Abnormalities of the peripheral blood as a presenting feature of immunodeficiency

American journal of hematology, 1978, Vol.4 (1), p.87-92

1978

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Activation of the alternative complement pathway by pneumococcal cell wall teichoic acid

The Journal of immunology (1950), 1978-01, Vol.120 (1), p.174-178

1978

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Activation of the Alternative Pathway by Pneumococcal Cell Wall Teichoic Acid

The Journal of immunology (1950), 1978-05, Vol.120 (5), p.1803-1803

1978

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Activation of the alternative pathway by pneumococcal cell walls

The Journal of immunology (1950), 1977-02, Vol.118 (2), p.451-454

1977

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Adenosine Deaminase Deficiency and Purine Nucleoside Phosphorylase Deficiency in Common Variable Immunodeficiency

Clinical and Diagnostic Laboratory Immunology, 1998-05, Vol.5 (3), p.399-400

1998

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Adenosine deaminase deficiency in adults

Blood, 1997-04, Vol.89 (8), p.2849-2855

1997

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Adults With X-Linked Agammaglobulinemia: Impact of Disease on Daily Lives, Quality of Life, Educational and Socioeconomic Status, Knowledge of Inheritance, and Reproductive Attitudes

Medicine (Baltimore), 2008-09, Vol.87 (5), p.253-258

2008

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Allergy, immunology, and related disorders

Current opinion in pediatrics, 1993-12, Vol.5 (6), p.681-683

1993

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Animal Model: Genetic Analysis of an Inherited Deficiency of the Third Component of Complement in Brittany Spaniel Dogs

American journal of medical genetics, 1986-11, Vol.25 (3), p.557-562

1986

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Are all IGIVs the same?

Journal of allergy and clinical immunology, 2002-12, Vol.110 (6), p.938-938

2002

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Association of homozygous C4B deficiency with bacterial meningitis

The Journal of infectious diseases, 1989-09, Vol.160 (3), p.448-451

1989

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B-Cell Defects: from X-linked Recessive to Autosomal Recessive Agammaglobulinemia

Primary Immunodeficiency Disorders, 2014

2014

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Bilateral consecutive central corneal perforations associated with hypogammaglobulinemia

Ophthalmology (Rochester, Minn.), 2000, Vol.107 (1), p.123-126

2000

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The binding of Pneumococcal lipoteichoic acid to human erythrocytes

Microbial pathogenesis, 1993-01, Vol.14 (1), p.23-31

1993

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THE BIOLOGIC SIGNIFICANCE OF THE THIRD COMPONENT OF COMPLEMENT (C3) IN NONIMMUNE HOST DEFENSES

Pediatric research, 1974-04, Vol.8 (4), p.421-421

1974

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Biological activities of tritiated endotoxins: correlation of the Limulus lysate assay with rabbit pyrogen and complement-activation assays for endotoxin

The Journal of laboratory and clinical medicine, 1977-02, Vol.89 (2), p.308

1977

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Carrier Detection in the Wiskott Aldrich Syndrome

Blood, 1988-11, Vol.72 (5), p.1735-1739

1988

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Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation

The New England journal of medicine, 1987-02, Vol.316 (8), p.427-431

1987

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Carrier detection of the X-linked primary immunodeficiency diseases using X-chromosome inactivation analysis

Journal of allergy and clinical immunology, 1990-06, Vol.85 (6), p.1090-1097

1990

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Chapter 11 - B-Cell Defects: From X-linked Recessive to Autosomal Recessive Agammaglobulinemia

Primary Immunodeficiency Disorders, 2015, p.127-138

2015

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1008 THEORETICAL AND BIOLOGICAL CONSIDERATIONS IN SUCCESSFUL MISMATCHED BONE MARROW TRANSPLANTATION

1010 LABORATORY FINDINGS IN VARIOUS CONGENITAL IMMUNODEFICIENCIES

105 - Infectious Complications of Complement Deficiencies

988 INDUCTION OF COMPLEMENT-MEDIATED DESTRUCTION OF HOST CELLS BY BACTERIAL LIPOTEICHOIC ACID

The ability of bacteria to activate the terminal complement components in serum of patients with cystic fibrosis

Abnormalities of the peripheral blood as a presenting feature of immunodeficiency

Activation of the alternative complement pathway by pneumococcal cell wall teichoic acid

Activation of the Alternative Pathway by Pneumococcal Cell Wall Teichoic Acid

Activation of the alternative pathway by pneumococcal cell walls

Adenosine Deaminase Deficiency and Purine Nucleoside Phosphorylase Deficiency in Common Variable Immunodeficiency

Adenosine deaminase deficiency in adults

Adults With X-Linked Agammaglobulinemia: Impact of Disease on Daily Lives, Quality of Life, Educational and Socioeconomic Status, Knowledge of Inheritance, and Reproductive Attitudes

Allergy, immunology, and related disorders

Animal Model: Genetic Analysis of an Inherited Deficiency of the Third Component of Complement in Brittany Spaniel Dogs

Are all IGIVs the same?

Association of homozygous C4B deficiency with bacterial meningitis

B-Cell Defects: from X-linked Recessive to Autosomal Recessive Agammaglobulinemia

Bilateral consecutive central corneal perforations associated with hypogammaglobulinemia

The binding of Pneumococcal lipoteichoic acid to human erythrocytes

THE BIOLOGIC SIGNIFICANCE OF THE THIRD COMPONENT OF COMPLEMENT (C3) IN NONIMMUNE HOST DEFENSES

Biological activities of tritiated endotoxins: correlation of the Limulus lysate assay with rabbit pyrogen and complement-activation assays for endotoxin

Carrier Detection in the Wiskott Aldrich Syndrome

Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation

Carrier detection of the X-linked primary immunodeficiency diseases using X-chromosome inactivation analysis

Chapter 11 - B-Cell Defects: From X-linked Recessive to Autosomal Recessive Agammaglobulinemia

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