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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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Influence of FCRN expression on lung decline and intravenous immunoglobulin catabolism in common variable immunodeficiency patients

Clinical and experimental immunology, 2014-12, Vol.178 (S1), p.103-104

Litzman, J.

2014

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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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Chronic immune activation in common variable immunodeficiency (CVID) is associated with elevated serum levels of soluble CD14 and CD25 but not endotoxaemia

Clinical and experimental immunology, 2012-12, Vol.170 (3), p.321-332

2012

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Low ficolin‐2 levels in common variable immunodeficiency patients with bronchiectasis

Clinical and experimental immunology, 2015-02, Vol.179 (2), p.256-264

2015

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Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients

Clinical and experimental immunology, 2013-04, Vol.172 (1), p.63-72

2013

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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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Sequence variants of the TNFRSF13B gene in Czech CVID and IgAD patients in the context of other populations

Human immunology, 2012-11, Vol.73 (11), p.1147-1154

2012

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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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Hereditary angio-oedema with C1 inhibitor deficiency: Characteristics and diagnostic delay of Czech patients from one centre

Allergologia et immunopathologia, 2016-05, Vol.44 (3), p.241-245

2016

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Association of FcRn expression with lung abnormalities and IVIG catabolism in patients with common variable immunodeficiency

Clinical immunology (Orlando, Fla.), 2010-09, Vol.136 (3), p.419-425

2010

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Reduced memory B cells in patients with hyper IgE syndrome

Clinical immunology (Orlando, Fla.), 2008-12, Vol.129 (3), p.448-454

2008

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Mannose-binding lectin gene polymorphic variants predispose to the development of bronchopulmonary complications but have no influence on other clinical and laboratory symptoms or signs of common variable immunodeficiency

Clinical and experimental immunology, 2008-09, Vol.153 (3), p.324-330

2008

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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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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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T and B lymphocyte subpopulations and activation/differentiation markers in patients with selective IgA deficiency

Clinical and experimental immunology, 2007-02, Vol.147 (2), p.249-254

2007

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No Evidence for Linkage between the Hereditary Angiooedema Clinical Phenotype and the BDKR1, BDKR2, ACE or MBL2 gene

Scandinavian journal of immunology, 2011-07, Vol.74 (1), p.100-106

2011

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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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No association of FCRN promoter VNTR polymorphism with the rate of maternal–fetal IgG transfer

Journal of reproductive immunology, 2010-06, Vol.85 (2), p.193-197

2010

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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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Mapping susceptibility gene locus for IgA deficiency at del(18)(q22.3-q23); report of familial cryptic chromosome t(18q; 10p) translocations

International Journal of Immunogenetics, 2007-06, Vol.34 (3), p.143-147

2007

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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

Influence of FCRN expression on lung decline and intravenous immunoglobulin catabolism in common variable immunodeficiency patients

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

Chronic immune activation in common variable immunodeficiency (CVID) is associated with elevated serum levels of soluble CD14 and CD25 but not endotoxaemia

Low ficolin‐2 levels in common variable immunodeficiency patients with bronchiectasis

Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients

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

Sequence variants of the TNFRSF13B gene in Czech CVID and IgAD patients in the context of other populations

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

Hereditary angio-oedema with C1 inhibitor deficiency: Characteristics and diagnostic delay of Czech patients from one centre

Association of FcRn expression with lung abnormalities and IVIG catabolism in patients with common variable immunodeficiency

Reduced memory B cells in patients with hyper IgE syndrome

Mannose-binding lectin gene polymorphic variants predispose to the development of bronchopulmonary complications but have no influence on other clinical and laboratory symptoms or signs of common variable immunodeficiency

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

NOD2 polymorphisms in clinical phenotypes of common variable immunodeficiency disorders

Recurrent meningitis and inherited complement deficiency

T and B lymphocyte subpopulations and activation/differentiation markers in patients with selective IgA deficiency

No Evidence for Linkage between the Hereditary Angiooedema Clinical Phenotype and the BDKR1, BDKR2, ACE or MBL2 gene

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

No association of FCRN promoter VNTR polymorphism with the rate of maternal–fetal IgG transfer

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

Mapping susceptibility gene locus for IgA deficiency at del(18)(q22.3-q23); report of familial cryptic chromosome t(18q; 10p) translocations

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