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Spectrum and Management of Complement Immunodeficiencies (Excluding Hereditary Angioedema) Across Europe

Journal of clinical immunology, 2015-02, Vol.35 (2), p.199-205

2015

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Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients (vol 172, pg 63, 2013)

Clinical and experimental immunology, 2013-07, Vol.173 (1), p.161

2013

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P165 Hereditary angioedema laryngeal attacks treated with recombinant C1-INH: report from the Czech National Registry

Annals of allergy, asthma, & immunology, 2017-11, Vol.119 (5), p.S43-S43

2017

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Primary immune deficiencies - principles of care

Frontiers in immunology, 2014-12, Vol.5, p.627-627

2014

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Recurrent Skin and Lung Infections in Autosomal Dominant Hyper IgE Syndrome with Transactivation Domain STAT3 Mutation

Case reports in immunology, 2014-01, Vol.2014, p.136752-5

2014

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Isoprinosine in the prevention of recurrent respiratory tract infections in childhood

Molecular immunology, 1998-08, Vol.35 (11), p.785-785

1998

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NOD2 polymorphisms in clinical phenotype of common variable immunodeficiency disorders

Clinical and experimental immunology, 2010, Vol.161 (3), p.536-541

2010

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ORIGINAL ARTICLE: Age dependency and mutual relations in T and B lymphocyte abnormalities in common variable immunodeficiency patients

Clinical and experimental immunology, 2006-02, Vol.143 (2), p.373-379

2006

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Gross Deletions Involving IGHM, BTK, or Artemis: A Model for Genomic Lesions Mediated by Trans posable Elements

American journal of human genetics, 2008-02, Vol.82 (2), p.320-332

2008

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Europe Immunoglobulin Map

JOURNAL OF CLINICAL IMMUNOLOGY, 2014, Vol.34, p.S155

2014

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Incidence and spectrum of primary immunodeficiency syndromes in the Czech Republic

Molecular immunology, 1998-08, Vol.35 (11), p.791-791

1998

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Immune system in children with di George syndrome

Molecular immunology, 1998-08, Vol.35 (11), p.733-733

1998

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Mutations in the signal transducer and activator of transcription 3 (STAT3) and diagnostic guidelines for the Hyper-IgE Syndrome

CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2010, Vol.160, p.4

2010

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Diagnostic criteria for the hyper IgE recurrent infection syndrome/Job's syndrome/STAT3 deficiency

CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2008, Vol.154, p.154

2008

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Defective integration of activating signals derived from the T cell receptor (TCR) and costimulatory molecules in both CD4 super(+) and CD8 super(+) T lymphocytes of common variable immunodeficiency (CVID) patients

Clinical and experimental immunology, 1997-11, Vol.110 (2), p.174-181

1997

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The costimulatory signal CD28 is fully functional but cannot correct the impaired angiten response in T cells of patients with common variable immunodeficiency

Clinical and experimental immunology, 1994, Vol.95 (2), p.209-214

1994

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A Case of Anti-SAE1 Dermatomyositis

Case reports in immunology, 2022, Vol.2022, p.9000608-4

2022

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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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Corrigendum: Clinical efficacy, safety and tolerability of a new subcutaneous immunoglobulin 16.5% (Octanorm [Cutaquig ® ]) in the treatment of patients with primary immunodeficiencies

Frontiers in immunology, 2022-12, Vol.13, p.1110388-1110388

2022

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Immunodeficiency in a Child with Rapadilino Syndrome: A Case Report and Review of the Literature

Case reports in immunology, 2015-01, Vol.2015, p.137368-4

2015

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Hyper‐IgE in the allergy clinic––when is it primary immunodeficiency?

Allergy (Copenhagen), 2018-11, Vol.73 (11), p.2122-2136

2018

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A Rose Amongst the Thorns: the Mission of the J Project in a Conflictual World

Journal of clinical immunology, 2022-08, Vol.42 (6), p.1151-1155

2022

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Fifteen Years of the J Project

Journal of clinical immunology, 2019-05, Vol.39 (4), p.363-369

2019

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The Konya Declaration for Patients with Primary Immunodeficiencies

Journal of clinical immunology, 2020-07, Vol.40 (5), p.770-773

2020

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The Wiskott-Aldrich syndrome protein is required for iNKT cell maturation and function

The Journal of cell biology, 2009-04, Vol.185 (1), p.i1-i1

2009

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Spectrum and Management of Complement Immunodeficiencies (Excluding Hereditary Angioedema) Across Europe

Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients (vol 172, pg 63, 2013)

P165 Hereditary angioedema laryngeal attacks treated with recombinant C1-INH: report from the Czech National Registry

Primary immune deficiencies - principles of care

Recurrent Skin and Lung Infections in Autosomal Dominant Hyper IgE Syndrome with Transactivation Domain STAT3 Mutation

Isoprinosine in the prevention of recurrent respiratory tract infections in childhood

NOD2 polymorphisms in clinical phenotype of common variable immunodeficiency disorders

ORIGINAL ARTICLE: Age dependency and mutual relations in T and B lymphocyte abnormalities in common variable immunodeficiency patients

Gross Deletions Involving IGHM, BTK, or Artemis: A Model for Genomic Lesions Mediated by Trans posable Elements

Europe Immunoglobulin Map

Incidence and spectrum of primary immunodeficiency syndromes in the Czech Republic

Immune system in children with di George syndrome

Mutations in the signal transducer and activator of transcription 3 (STAT3) and diagnostic guidelines for the Hyper-IgE Syndrome

Diagnostic criteria for the hyper IgE recurrent infection syndrome/Job's syndrome/STAT3 deficiency

Defective integration of activating signals derived from the T cell receptor (TCR) and costimulatory molecules in both CD4 super(+) and CD8 super(+) T lymphocytes of common variable immunodeficiency (CVID) patients

The costimulatory signal CD28 is fully functional but cannot correct the impaired angiten response in T cells of patients with common variable immunodeficiency

A Case of Anti-SAE1 Dermatomyositis

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

Corrigendum: Clinical efficacy, safety and tolerability of a new subcutaneous immunoglobulin 16.5% (Octanorm [Cutaquig ® ]) in the treatment of patients with primary immunodeficiencies

Immunodeficiency in a Child with Rapadilino Syndrome: A Case Report and Review of the Literature

Hyper‐IgE in the allergy clinic––when is it primary immunodeficiency?

A Rose Amongst the Thorns: the Mission of the J Project in a Conflictual World

Fifteen Years of the J Project

The Konya Declaration for Patients with Primary Immunodeficiencies

The Wiskott-Aldrich syndrome protein is required for iNKT cell maturation and function

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