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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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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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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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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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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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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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Recurrent laryngeal papillomatosis: successful treatment with human papillomavirus vaccination

Archives of disease in childhood, 2011-05, Vol.96 (5), p.476-477

2011

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Secondary Combined Immunodeficiency in Pediatric Patients after the Fontan Operation: Three Case Reports

International archives of allergy and immunology, 2016-11, Vol.170 (4), p.251-256

2016

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European internet-based patient and research database for primary immunodeficiencies: results 2006-2008

Clinical and experimental immunology, 2009-09, Vol.157 (Supplement_1), p.3-11

2009

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IgA Deficiency in Czech Healthy Individuals and Selected Patient Groups

International archives of allergy and immunology, 2000-10, Vol.123 (2), p.177-180

2000

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ICOS deficiency in patients with common variable immunodeficiency

Clinical immunology (Orlando, Fla.), 2004-12, Vol.113 (3), p.234-240

2004

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Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency

Clinical immunology (Orlando, Fla.), 2004, Vol.110 (1), p.22-29

2004

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Early manifestation and recognition of C2 complement deficiency in the form of pyogenic infection in infancy

Journal of paediatrics and child health, 2003-05, Vol.39 (4), p.274-277

2003

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Isoprinosine does not protect against frequent respiratory tract infections in childhood

European journal of pediatrics, 1999, Vol.158 (1), p.32-37

1999

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Common variable immunodeficiency in pregnancy (set of case reports)

Ceská gynekologie, 2009-06, Vol.74 (3), p.197

2009

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Agammaglobulinaemia in a girl with a mosaic of ring 18 chromosome

Journal of paediatrics and child health, 1998-02, Vol.34 (1), p.92-94

1998

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

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

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

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

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

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

Recurrent laryngeal papillomatosis: successful treatment with human papillomavirus vaccination

Secondary Combined Immunodeficiency in Pediatric Patients after the Fontan Operation: Three Case Reports

European internet-based patient and research database for primary immunodeficiencies: results 2006-2008

IgA Deficiency in Czech Healthy Individuals and Selected Patient Groups

ICOS deficiency in patients with common variable immunodeficiency

Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency

Early manifestation and recognition of C2 complement deficiency in the form of pyogenic infection in infancy

Isoprinosine does not protect against frequent respiratory tract infections in childhood

Common variable immunodeficiency in pregnancy (set of case reports)

Agammaglobulinaemia in a girl with a mosaic of ring 18 chromosome

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