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A Critical View of Specific Antibody Deficiencies

Frontiers in immunology, 2019-05, Vol.10, p.986-986

Sorensen, Ricardo U

2019

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Practice parameter for the diagnosis and management of primary immunodeficiency

Journal of allergy and clinical immunology, 2015-11, Vol.136 (5), p.1186-1205.e78

2015

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Bronchiectasis in Primary Antibody Deficiencies: A Multidisciplinary Approach

Frontiers in immunology, 2020-03, Vol.11, p.522-522

2020

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BCG: a vaccine with multiple faces

Human vaccines & immunotherapeutics, 2020-08, Vol.16 (8), p.1841-1850

2020

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Assessment and clinical interpretation of polysaccharide antibody responses

Annals of Allergy, Asthma & Immunology, 2007-11, Vol.99 (5), p.462-464

2007

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Novel mechanism for the generation of human xeno-autoantibodies against the nonhuman sialic acid N-glycolylneuraminic acid

The Journal of experimental medicine, 2010-08, Vol.207 (8), p.1637-1646

2010

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Attending to Warning Signs of Primary Immunodeficiency Diseases Across the Range of Clinical Practice

Journal of clinical immunology, 2014-01, Vol.34 (1), p.10-22

2014

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Practice parameter for the diagnosis and management of primary immunodeficiency

Annals of allergy, asthma, & immunology, 2005-05, Vol.94 (5), p.S1-S63

2005

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Specific Antibody Deficiencies

Immunology and allergy clinics of North America, 2015-11, Vol.35 (4), p.659-670

2015

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Recurrent Respiratory Infections, Specific Antibody Deficiencies, and Memory B Cells

Journal of clinical immunology, 2013-01, Vol.33 (Suppl 1), p.57-61

2013

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Atopic Dermatitis: Looking Beyond the Skin

The Journal of pediatrics, 2013-12, Vol.163 (6), p.1547-1548

2013

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Specific Antibody Deficiencies in Clinical Practice

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2019-03, Vol.7 (3), p.801-808

2019

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Overview of antibody‐mediated immunity to S. pneumoniae: pneumococcal infections, pneumococcal immunity assessment, and recommendations for IG product evaluation

Transfusion (Philadelphia, Pa.), 2018-12, Vol.58 (S3), p.3106-3113

2018

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Influenza immunization in patients with common variable immunodeficiency

Journal of allergy and clinical immunology, 2018-12, Vol.142 (6), p.1759-1761

2018

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Development of multiple food allergies in children taking tacrolimus after heart and liver transplantation

Pediatric transplantation, 2006-05, Vol.10 (3), p.380-383

2006

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Congenital alterations of NEMO glutamic acid 223 result in hypohidrotic ectodermal dysplasia and immunodeficiency with normal serum IgG levels

Annals of allergy, asthma, & immunology, 2011-07, Vol.107 (1), p.50-56

2011

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Use of intravenous immunoglobulin in human disease: A review of evidence by members of the Primary Immunodeficiency Committee of the American Academy of Allergy, Asthma and Immunology

Journal of Allergy and Clinical Immunology, 2006-04, Vol.117 (4), p.S525-S553

2006

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Severe SOPH syndrome due to a novel NBAS mutation in a 27‐year‐old woman—Review of this pleiotropic, autosomal recessive disorder: Mystery solved after two decades

American journal of medical genetics. Part A, 2020-07, Vol.182 (7), p.1767-1775

2020

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The actin regulator coronin 1A is mutant in a thymic egress-deficient mouse strain and in a patient with severe combined immunodeficiency

Nature immunology, 2008-11, Vol.9 (11), p.1307-1315

2008

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Global study of primary immunodeficiency diseases (PI)—diagnosis, treatment, and economic impact: an updated report from the Jeffrey Modell Foundation

Immunologic research, 2011-10, Vol.51 (1), p.61-70

2011

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Prescribing Immunoglobulin Replacement Therapy for Patients with Non-classical and Secondary Antibody Deficiency: an Analysis of the Practice of Clinical Immunologists in the UK and Republic of Ireland

Journal of clinical immunology, 2018-02, Vol.38 (2), p.204-213

2018

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Severe combined immunodeficiency (SCID) and attention deficit hyperactivity disorder (ADHD) associated with a coronin-1A mutation and a chromosome 16p11.2 deletion

Clinical immunology (Orlando, Fla.), 2009-04, Vol.131 (1), p.24-30

2009

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Measurement of Pneumococcal Polysaccharide Antibodies

Journal of clinical immunology, 2014-02, Vol.34 (2), p.127-128

2014

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A Critical View of Specific Antibody Deficiencies

Use and interpretation of diagnostic vaccination in primary immunodeficiency: A working group report of the Basic and Clinical Immunology Interest Section of the American Academy of Allergy, Asthma & Immunology

Practice parameter for the diagnosis and management of primary immunodeficiency

Bronchiectasis in Primary Antibody Deficiencies: A Multidisciplinary Approach

BCG: a vaccine with multiple faces

Assessment and clinical interpretation of polysaccharide antibody responses

Novel mechanism for the generation of human xeno-autoantibodies against the nonhuman sialic acid N-glycolylneuraminic acid

Exploring the Impact of Ketodeoxynonulosonic Acid in Host-Pathogen Interactions Using Uptake and Surface Display by Nontypeable Haemophilus influenzae

Attending to Warning Signs of Primary Immunodeficiency Diseases Across the Range of Clinical Practice

Practice parameter for the diagnosis and management of primary immunodeficiency

Specific Antibody Deficiencies

Recurrent Respiratory Infections, Specific Antibody Deficiencies, and Memory B Cells

Atopic Dermatitis: Looking Beyond the Skin

Specific Antibody Deficiencies in Clinical Practice

Overview of antibody‐mediated immunity to S. pneumoniae: pneumococcal infections, pneumococcal immunity assessment, and recommendations for IG product evaluation

Influenza immunization in patients with common variable immunodeficiency

Development of multiple food allergies in children taking tacrolimus after heart and liver transplantation

Congenital alterations of NEMO glutamic acid 223 result in hypohidrotic ectodermal dysplasia and immunodeficiency with normal serum IgG levels

Use of intravenous immunoglobulin in human disease: A review of evidence by members of the Primary Immunodeficiency Committee of the American Academy of Allergy, Asthma and Immunology

Severe SOPH syndrome due to a novel NBAS mutation in a 27‐year‐old woman—Review of this pleiotropic, autosomal recessive disorder: Mystery solved after two decades

The actin regulator coronin 1A is mutant in a thymic egress-deficient mouse strain and in a patient with severe combined immunodeficiency

Global study of primary immunodeficiency diseases (PI)—diagnosis, treatment, and economic impact: an updated report from the Jeffrey Modell Foundation

Prescribing Immunoglobulin Replacement Therapy for Patients with Non-classical and Secondary Antibody Deficiency: an Analysis of the Practice of Clinical Immunologists in the UK and Republic of Ireland

Severe combined immunodeficiency (SCID) and attention deficit hyperactivity disorder (ADHD) associated with a coronin-1A mutation and a chromosome 16p11.2 deletion

Measurement of Pneumococcal Polysaccharide Antibodies

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