List of works - Susanne Unger

Autosomal dominant gain of function STAT1 mutation and severe bronchiectasis

scientific article published on 22 March 2017

Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations

scientific article

Common variable immunodeficiency (CVID): exploring the multiple dimensions of a heterogeneous disease.

scientific article published on 02 February 2012

Correction: Early onset combined immunodeficiency and autoimmunity in patients with loss-of-function mutation in LAT.

scientific article published on June 2017

Cytokines in common variable immunodeficiency as signs of immune dysregulation and potential therapeutic targets - a review of the current knowledge

scientific article published on 15 May 2014

Early onset combined immunodeficiency and autoimmunity in patients with loss-of-function mutation in LAT.

scientific article published on 30 May 2016

Enteroviral Infection in a Patient with BLNK Adaptor Protein Deficiency.

scientific article published on 17 April 2015

Extending the clinical and immunological phenotype of human interleukin-21 receptor deficiency.

scientific article published on 14 November 2014

Generalized verrucosis and HPV-3 susceptibility associated with CD4 T-cell lymphopenia caused by inherited human interleukin-7 deficiency

scientific article published on 01 June 2015

High levels of SOX5 decrease proliferative capacity of human B cells, but permit plasmablast differentiation.

scientific article

Ill-defined germinal centers and severely reduced plasma cells are histological hallmarks of lymphadenopathy in patients with common variable immunodeficiency.

scientific article published on 2 May 2014

Increase of circulating α4β7+ conventional memory CD4 and regulatory T cells in patients with common variable immunodeficiency (CVID).

scientific article

Preferential Reduction of Circulating Innate Lymphoid Cells Type 2 in Patients with Common Variable Immunodeficiency with Secondary Complications Is Part of a Broader Immune Dysregulation.

scientific article published on 21 September 2017

Secondary Antibody Deficiency in Glucocorticoid Therapy Clearly Differs from Primary Antibody Deficiency

scientific article

The TH1 phenotype of follicular helper T cells indicates an IFN-γ-associated immune dysregulation in patients with CD21low common variable immunodeficiency.

scientific article published on 26 May 2017

β2-Microglobulin deficiency causes a complex immunodeficiency of the innate and adaptive immune system.

scientific article published on 19 February 2015

List of works by Susanne Unger

Autosomal dominant gain of function STAT1 mutation and severe bronchiectasis

Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations

Common variable immunodeficiency (CVID): exploring the multiple dimensions of a heterogeneous disease.

Correction: Early onset combined immunodeficiency and autoimmunity in patients with loss-of-function mutation in LAT.

Cytokines in common variable immunodeficiency as signs of immune dysregulation and potential therapeutic targets - a review of the current knowledge

Early onset combined immunodeficiency and autoimmunity in patients with loss-of-function mutation in LAT.

Enteroviral Infection in a Patient with BLNK Adaptor Protein Deficiency.

Extending the clinical and immunological phenotype of human interleukin-21 receptor deficiency.

Generalized verrucosis and HPV-3 susceptibility associated with CD4 T-cell lymphopenia caused by inherited human interleukin-7 deficiency

High levels of SOX5 decrease proliferative capacity of human B cells, but permit plasmablast differentiation.

Ill-defined germinal centers and severely reduced plasma cells are histological hallmarks of lymphadenopathy in patients with common variable immunodeficiency.

Increase of circulating α4β7+ conventional memory CD4 and regulatory T cells in patients with common variable immunodeficiency (CVID).

Preferential Reduction of Circulating Innate Lymphoid Cells Type 2 in Patients with Common Variable Immunodeficiency with Secondary Complications Is Part of a Broader Immune Dysregulation.

Secondary Antibody Deficiency in Glucocorticoid Therapy Clearly Differs from Primary Antibody Deficiency

The TH1 phenotype of follicular helper T cells indicates an IFN-γ-associated immune dysregulation in patients with CD21low common variable immunodeficiency.

β2-Microglobulin deficiency causes a complex immunodeficiency of the innate and adaptive immune system.