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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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When to initiate immunoglobulin replacement therapy (IGRT) in antibody deficiency: a practical approach

Clinical and experimental immunology, 2017-06, Vol.188 (3), p.333-341

2017

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Common variants at PVT1, ATG13–AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency

Nature genetics, 2016-11, Vol.48 (11), p.1425-1429

2016

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Possibilities for the analysis of peripheral blood B cell subpopulations in a routine immunological laboratory

Epidemiologie, mikrobiologie, imunologie, 2021, Vol.70 (4), p.264

2021

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Matrix metalloproteinase-9 and matrix metalloproteinase-2 as biomarkers of various courses in multiple sclerosis

Multiple sclerosis, 2009-03, Vol.15 (3), p.316-322

2009

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NOD2 polymorphisms in clinical phenotypes of common variable immunodeficiency disorders

Clinical and experimental immunology, 2010-09, Vol.161 (3), p.536-541

2010

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Recurrent meningitis and inherited complement deficiency

Epidemiologie, mikrobiologie, imunologie, 2016, Vol.65 (4), p.238

2016

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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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Neutrophils Are Dysregulated in Patients with Hereditary Angioedema Types I and II in a Symptom-Free Period

Mediators of inflammation, 2019-01, Vol.2019 (2019), p.1-12

2019

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CEBPE -Mutant Specific Granule Deficiency Correlates With Aberrant Granule Organization and Substantial Proteome Alterations in Neutrophils

Frontiers in immunology, 2018-03, Vol.9 (MAR), p.588-588

2018

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A simple method for the detection of CD154 (CD40L) on peripheral blood lymphocytes

Epidemiologie, mikrobiologie, imunologie, 2010-08, Vol.59 (3), p.147

2010

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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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Intravenous immunoglobulin, splenectomy, and antibiotic prophylaxis in Wiskott-Aldrich syndrome

Archives of disease in childhood, 1996-11, Vol.75 (5), p.436-439

1996

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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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Negativity for Specific Autoantibodies in Patients with Type 1 Diabetes That Developed on a Background of Common Variable Immunodeficiency

International archives of allergy and immunology, 2016-03, Vol.168 (3), p.197-204

2016

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Defective integration of activating signals derived from the T cell receptor (TCR) and costimulatory molecules in both CD4+ and CD8+ 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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Recurrent Skin and Lung Infections in Autosomal Dominant Hyper IgE Syndrome with Transactivation Domain STAT3 Mutation

Case reports in immunology, 2014-01, Vol.2014 (2014), p.1-5

2014

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Antigen presentation by common variable immunodeficiency (CVID) B cells and monocytes is unimpaired

Clinical and experimental immunology, 1997-04, Vol.108 (1), p.1-8

1997

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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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Serum IgD levels in children under investigation for and with defined immunodeficiency

International archives of allergy and immunology, 1997-01, Vol.114 (1), p.54-58

1997

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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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The mechanism of erythrocyte sedimentation in Westergren's examination

Biorheology (Oxford), 1992-03, Vol.29 (2-3), p.261-271

1992

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Europe Immunoglobulin Map

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

2014

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

When to initiate immunoglobulin replacement therapy (IGRT) in antibody deficiency: a practical approach

Common variants at PVT1, ATG13–AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency

Possibilities for the analysis of peripheral blood B cell subpopulations in a routine immunological laboratory

Matrix metalloproteinase-9 and matrix metalloproteinase-2 as biomarkers of various courses in multiple sclerosis

NOD2 polymorphisms in clinical phenotypes of common variable immunodeficiency disorders

Recurrent meningitis and inherited complement deficiency

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

Neutrophils Are Dysregulated in Patients with Hereditary Angioedema Types I and II in a Symptom-Free Period

CEBPE -Mutant Specific Granule Deficiency Correlates With Aberrant Granule Organization and Substantial Proteome Alterations in Neutrophils

A simple method for the detection of CD154 (CD40L) on peripheral blood lymphocytes

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

Intravenous immunoglobulin, splenectomy, and antibiotic prophylaxis in Wiskott-Aldrich syndrome

Primary immune deficiencies - principles of care

Negativity for Specific Autoantibodies in Patients with Type 1 Diabetes That Developed on a Background of Common Variable Immunodeficiency

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

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

Antigen presentation by common variable immunodeficiency (CVID) B cells and monocytes is unimpaired

Isoprinosine in the prevention of recurrent respiratory tract infections in childhood

Serum IgD levels in children under investigation for and with defined immunodeficiency

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

The mechanism of erythrocyte sedimentation in Westergren's examination

Europe Immunoglobulin Map

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