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European Society for Immunodeficiencies (ESID) and European Reference Network on Rare Primary Immunodeficiency, Autoinflammatory and Autoimmune Diseases (ERN RITA) Complement Guideline: Deficiencies, Diagnosis, and Management

Journal of clinical immunology, 2020-05, Vol.40 (4), p.576-591

2020

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A Randomized, Double-Blind, Phase III Study of the Immunogenicity and Safety of a 9-Valent Human Papillomavirus L1 Virus-Like Particle Vaccine (V503) Versus Gardasil® in 9-15-Year-Old Girls

The Pediatric infectious disease journal, 2015-09, Vol.34 (9), p.992-998

2015

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The international WAO/EAACI guideline for the management of hereditary angioedema – The 2021 revision and update

The World Allergy Organization journal, 2022-03, Vol.15 (3), p.100627-100627, Article 100627

2022

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Diagnosis of immunodeficiency caused by a purine nucleoside phosphorylase defect by using tandem mass spectrometry on dried blood spots

Journal of allergy and clinical immunology, 2014-07, Vol.134 (1), p.155-159.e3

2014

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Add-on or alone? Inhaled nebulized immunoglobulin reduces upper airway infections: 24 months of real-life experience

Immunotherapy, 2020-04, Vol.12 (6), p.389-394

Brodszki, Nicholas

2020

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First Year of TREC-Based National SCID Screening in Sweden

International journal of neonatal screening, 2021-08, Vol.7 (3), p.59

2021

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Analysis of Safety and Tolerability Data in Pediatric Patients with Primary Immunodeficiency Diseases from Two Phase 2/3 Studies of Human Immune Globulin Subcutaneous, 20

Journal of allergy and clinical immunology, 2017-02, Vol.139 (2), p.AB217-AB217

2017

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Best Possible Treatment for All Patients with Primary Immune Deficiency (PID) in Sweden Regardless of Social Factors, Sex, Age or Residence

Journal of allergy and clinical immunology, 2017-02, Vol.139 (2), p.AB249-AB249

2017

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A New Subcutaneous Immunoglobulin 20% Formulation (SCIG 20%) with Individualized Infusion Parameters Resulted in a Positive Safety and Tolerability Profile in Patients with PIDD in Europe and North America

Journal of allergy and clinical immunology, 2017-02, Vol.139 (2), p.AB216-AB216

2017

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The international WAO/EAACI guideline for the management of hereditary angioedema—The 2021 revision and update

Allergy (Copenhagen), 2022-07, Vol.77 (7), p.1961-1990

2022

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Immunologic Control of Disseminated Aichi Virus Infection in X-Linked Agammaglobulinemia by Transplantation of TcRαβ-Depleted Haploidentical Hematopoietic Cells

Journal of clinical immunology, 2022-10, Vol.42 (7), p.1401-1404

2022

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Novel treatment of severe combined immunodeficiency utilizing ex-vivo T-cell depleted haploidentical hematopoietic stem cell transplantation and CD45RA+ depleted donor lymphocyte infusions

Orphanet journal of rare diseases, 2016-01, Vol.11 (5), p.5-5, Article 5

2016

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Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study

Journal of allergy and clinical immunology, 2016-07, Vol.138 (1), p.210-218.e9

2016

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The European internet‐based patient and research database for primary immunodeficiencies: update 2011

Clinical and experimental immunology, 2012-03, Vol.167 (3), p.479-491

2012

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Immune responses following meningococcal serogroups A, C, Y and W polysaccharide vaccination in C2-deficient persons: Evidence for increased levels of serum bactericidal antibodies

Vaccine, 2015-04, Vol.33 (15), p.1839-1845

2015

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Kappa‐deleting recombination excision circle levels remain low or undetectable throughout life in patients with X‐linked agammaglobulinemia

Pediatric allergy and immunology, 2018-06, Vol.29 (4), p.453-456

2018

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Safety and tolerability of subcutaneous immunoglobulin 20% in primary immunodeficiency diseases from two continents

Immunotherapy, 2019-08, Vol.11 (12), p.1057-1065

2019

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Primary immunodeficiency in infection-prone children in southern Sweden: occurrence, clinical characteristics and immunological findings

BMC immunology, 2014-08, Vol.15 (1), p.31-31, Article 31

2014

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Immunologic findings in young children with early onset of acute otitis media

Acta oto-laryngologica, 2014-10, Vol.134 (10), p.1022-1028

2014

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Definition, aims, and implementation of GA2LEN/HAEi Angioedema Centers of Reference and Excellence

Allergy (Copenhagen), 2020-08, Vol.75 (8), p.2115-n/a

2020

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A Core Outcome Set for Efficacy of Acute Treatment of Hereditary Angioedema

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2024-06, Vol.12 (6), p.1614-1621

2024

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Tolerability of subcutaneous immunoglobulin 20%, Ig20Gly, in pediatric patients with primary immunodeficiencies

Immunotherapy, 2019-04, Vol.11 (5), p.397-406

2019

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Pulmonary and pleural lymphatic endothelial cells from pediatric, but not adult, patients with Gorham-Stout disease and generalized lymphatic anomaly, show a high proliferation rate

Orphanet journal of rare diseases, 2016-05, Vol.11 (1), p.67-67, Article 67

2016

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A novel treatment approach for paediatric Gorham-Stout syndrome with chylothorax

Acta Paediatrica, 2011-11, Vol.100 (11), p.1448-1453

2011

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Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase [delta] syndrome 2: A cohort study

Journal of allergy and clinical immunology, 2016-07, Vol.138 (1), p.210

2016

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European Society for Immunodeficiencies (ESID) and European Reference Network on Rare Primary Immunodeficiency, Autoinflammatory and Autoimmune Diseases (ERN RITA) Complement Guideline: Deficiencies, Diagnosis, and Management

A Randomized, Double-Blind, Phase III Study of the Immunogenicity and Safety of a 9-Valent Human Papillomavirus L1 Virus-Like Particle Vaccine (V503) Versus Gardasil® in 9-15-Year-Old Girls

The international WAO/EAACI guideline for the management of hereditary angioedema – The 2021 revision and update

Diagnosis of immunodeficiency caused by a purine nucleoside phosphorylase defect by using tandem mass spectrometry on dried blood spots

Add-on or alone? Inhaled nebulized immunoglobulin reduces upper airway infections: 24 months of real-life experience

First Year of TREC-Based National SCID Screening in Sweden

Analysis of Safety and Tolerability Data in Pediatric Patients with Primary Immunodeficiency Diseases from Two Phase 2/3 Studies of Human Immune Globulin Subcutaneous, 20

Best Possible Treatment for All Patients with Primary Immune Deficiency (PID) in Sweden Regardless of Social Factors, Sex, Age or Residence

A New Subcutaneous Immunoglobulin 20% Formulation (SCIG 20%) with Individualized Infusion Parameters Resulted in a Positive Safety and Tolerability Profile in Patients with PIDD in Europe and North America

The international WAO/EAACI guideline for the management of hereditary angioedema—The 2021 revision and update

Immunologic Control of Disseminated Aichi Virus Infection in X-Linked Agammaglobulinemia by Transplantation of TcRαβ-Depleted Haploidentical Hematopoietic Cells

Novel treatment of severe combined immunodeficiency utilizing ex-vivo T-cell depleted haploidentical hematopoietic stem cell transplantation and CD45RA+ depleted donor lymphocyte infusions

Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study

The European internet‐based patient and research database for primary immunodeficiencies: update 2011

Immune responses following meningococcal serogroups A, C, Y and W polysaccharide vaccination in C2-deficient persons: Evidence for increased levels of serum bactericidal antibodies

Kappa‐deleting recombination excision circle levels remain low or undetectable throughout life in patients with X‐linked agammaglobulinemia

Safety and tolerability of subcutaneous immunoglobulin 20% in primary immunodeficiency diseases from two continents

Primary immunodeficiency in infection-prone children in southern Sweden: occurrence, clinical characteristics and immunological findings

Immunologic findings in young children with early onset of acute otitis media

Definition, aims, and implementation of GA2LEN/HAEi Angioedema Centers of Reference and Excellence

A Core Outcome Set for Efficacy of Acute Treatment of Hereditary Angioedema

Tolerability of subcutaneous immunoglobulin 20%, Ig20Gly, in pediatric patients with primary immunodeficiencies

Pulmonary and pleural lymphatic endothelial cells from pediatric, but not adult, patients with Gorham-Stout disease and generalized lymphatic anomaly, show a high proliferation rate

A novel treatment approach for paediatric Gorham-Stout syndrome with chylothorax

Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase [delta] syndrome 2: A cohort study

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