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MicroRNA-146a reduces MHC-II expression via targeting JAK/STAT signaling in dendritic cells after stem cell transplantation

Leukemia, 2017-12, Vol.31 (12), p.2732-2741

2017

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X-linked inhibitor of apoptosis (XIAP) deficiency: The spectrum of presenting manifestations beyond hemophagocytic lymphohistiocytosis

Clinical immunology (Orlando, Fla.), 2013-10, Vol.149 (1), p.133-141

2013

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Activating PI3K[delta] mutations in a cohort of 669 patients with primary immunodeficiency

Clinical and experimental immunology, 2016-02, Vol.183 (2), p.221

2016

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Stomatin, flotillin-1, and flotillin-2 are major integral proteins of erythrocyte lipid rafts

Blood, 2001-02, Vol.97 (4), p.1141-1143

2001

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Activating PI3Kδ mutations in a cohort of 669 patients with primary immunodeficiency

Clinical and experimental immunology, 2016-02, Vol.183 (2), p.221-229

2016

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Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans

Nature genetics, 2005-08, Vol.37 (8), p.820-828

2005

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THU0380 Diagnostic utility of anti-dfs-70 autoantibodies in a university rheumatology centre

Annals of the rheumatic diseases, 2018-06, Vol.77 (Suppl 2), p.406

2018

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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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SAT0327 B Cell-Bound Complement Activation Products in The Diagnosis and Monitoring of Systemic Lupus Erythematosus

Annals of the rheumatic diseases, 2016-06, Vol.75 (Suppl 2), p.785-786

2016

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SAT0415 The mrz reaction helps to distinguish rheumatologic disorders with central nervous involvement from multiple sclerosis

Annals of the rheumatic diseases, 2018-06, Vol.77 (Suppl 2), p.1068

2018

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Chilblain lupus and steroid‐responsive pancytopenia precede monosomy 7‐linked AML as manifestation of rasopathy

Pediatric blood & cancer, 2017-12, Vol.64 (12), p.n/a

2017

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Incidence of thrombotic and bleeding complications during cardiac catheterization in children: comparison of high‐dose vs. low‐dose heparin protocols

Journal of thrombosis and haemostasis, 2011-12, Vol.9 (12), p.2353-2360

2011

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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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Active vaccination in patients with common variable immunodeficiency (CVID)

Clinical Immunology, 2007-09, Vol.124 (3), p.294-303

2007

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SAT0163 B-Cell Homeostasis is Disturbed by Immunosuppressive Therapies and After Treatment with Rituximab in Patients with Anca-Associated Vasculitides

Annals of the rheumatic diseases, 2013-06, Vol.72 (Suppl 3), p.A637-A637

2013

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Clinical and immunological overlap between autoimmune lymphoproliferative syndrome and common variable immunodeficiency

Clinical immunology (Orlando, Fla.), 2010-12, Vol.137 (3), p.357-365

2010

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Danon disease: Case report and detection of new mutation

Journal of inherited metabolic disease, 2009-12, Vol.32 (Suppl 1), p.115-122

2009

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A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family

Human immunology, 2012-08, Vol.73 (8), p.836-839

2012

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THU0017 The Role of HLA DQ2 and DQ8 in Dissecting Celiac-Like Disease in Common Variable Immunodeficiency

Annals of the rheumatic diseases, 2013-06, Vol.72 (Suppl 3), p.A170-A170

2013

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FRI0235 Alterations in peripheral B cell subsets of patients with anca associated vasculitides (AAVS) after immunosuppressive therapy

Annals of the rheumatic diseases, 2013-06, Vol.71 (Suppl 3), p.393-394

2013

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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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Monozygotic twins with stiff person syndrome and autoimmune thyroiditis: rituximab inefficacy in a double-blind, randomised, placebo controlled crossover study

Annals of the rheumatic diseases, 2009-09, Vol.68 (9), p.1506-1508

2009

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P-018 Exome-sequencing identifies acquired mutations in ASXL1, PHF6 and DOCK5 as secondary genetic events in a case of germline GATA2-mutation

Leukemia research, 2013-05, Vol.37, p.S31-S31

2013

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Early failure of the tissue engineered porcine heart valve SYNERGRAFT® in pediatric patients

European journal of cardio-thoracic surgery, 2003-06, Vol.23 (6), p.1002-1006

2003

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MicroRNA-146a reduces MHC-II expression via targeting JAK/STAT signaling in dendritic cells after stem cell transplantation

X-linked inhibitor of apoptosis (XIAP) deficiency: The spectrum of presenting manifestations beyond hemophagocytic lymphohistiocytosis

Activating PI3K[delta] mutations in a cohort of 669 patients with primary immunodeficiency

Stomatin, flotillin-1, and flotillin-2 are major integral proteins of erythrocyte lipid rafts

Activating PI3Kδ mutations in a cohort of 669 patients with primary immunodeficiency

Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans

THU0380 Diagnostic utility of anti-dfs-70 autoantibodies in a university rheumatology centre

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

SAT0327 B Cell-Bound Complement Activation Products in The Diagnosis and Monitoring of Systemic Lupus Erythematosus

SAT0415 The mrz reaction helps to distinguish rheumatologic disorders with central nervous involvement from multiple sclerosis

Chilblain lupus and steroid‐responsive pancytopenia precede monosomy 7‐linked AML as manifestation of rasopathy

Incidence of thrombotic and bleeding complications during cardiac catheterization in children: comparison of high‐dose vs. low‐dose heparin protocols

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

Active vaccination in patients with common variable immunodeficiency (CVID)

SAT0163 B-Cell Homeostasis is Disturbed by Immunosuppressive Therapies and After Treatment with Rituximab in Patients with Anca-Associated Vasculitides

Clinical and immunological overlap between autoimmune lymphoproliferative syndrome and common variable immunodeficiency

Danon disease: Case report and detection of new mutation

A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family

THU0017 The Role of HLA DQ2 and DQ8 in Dissecting Celiac-Like Disease in Common Variable Immunodeficiency

FRI0235 Alterations in peripheral B cell subsets of patients with anca associated vasculitides (AAVS) after immunosuppressive therapy

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

Monozygotic twins with stiff person syndrome and autoimmune thyroiditis: rituximab inefficacy in a double-blind, randomised, placebo controlled crossover study

P-018 Exome-sequencing identifies acquired mutations in ASXL1, PHF6 and DOCK5 as secondary genetic events in a case of germline GATA2-mutation

Early failure of the tissue engineered porcine heart valve SYNERGRAFT® in pediatric patients

Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity

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