List of works - Ulrich Salzer

A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency.

scientific article published on 7 January 2014

A feeder-free differentiation system identifies autonomously proliferating B cell precursors in human bone marrow

scientific article published on 30 December 2013

A homozygous CARD9 mutation in a family with susceptibility to fungal infections

scientific article

A novel disease-causing synonymous exonic mutation in GATA2 affecting RNA splicing

scientific article published on 20 July 2018

A syndrome with congenital neutropenia and mutations in G6PC3

scientific article

Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells

scientific article published on 20 April 2015

Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations

scientific article

B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans.

scholarly article

B-cell signaling in persistent polyclonal B lymphocytosis (PPBL).

scientific article

BAFF- and TACI-Dependent Processing of BAFFR by ADAM Proteases Regulates the Survival of B Cells

scientific article published in February 2017

Cast Nephropathy and Deceptively Low Absolute Serum Free Light Chain Levels: Resolution of a Challenging Case and Systematic Review of the Literature

scientific article published on 3 October 2017

Circulating CD21low B cells in common variable immunodeficiency resemble tissue homing, innate-like B cells.

scholarly article

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

scientific article published on 02 February 2012

Common variable immunodeficiency - an update ⬇️

scientific article published on September 24, 2012

Common variable immunodeficiency at the end of a prospering decade: towards novel gene defects and beyond ⬇️

scientific article published on December 1, 2010

Common variable immunodeficiency: The power of co-stimulation.

scientific article published on 4 October 2006

Common variable immunodeficiency: a multifaceted and puzzling disorder

scientific article published on 01 March 2009

DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency.

scientific article

Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity

scientific article

Diffuse parenchymal lung disease as first clinical manifestation of GATA-2 deficiency in childhood.

scientific article

Fatal adult-onset antibody deficiency syndrome in a patient with cartilage hair hypoplasia

scientific article published on 09 June 2010

Gray platelet syndrome can mimic autoimmune lymphoproliferative syndrome

scientific article published in October 2015

Heterozygous alterations of TNFRSF13B/TACI in tonsillar hypertrophy and sarcoidosis.

scientific article published on 15 July 2013

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

scientific article

Human ICOS deficiency abrogates the germinal center reaction and provides a monogenic model for common variable immunodeficiency

scientific article published on 29 December 2005

ICOS deficiency in patients with common variable immunodeficiency.

scientific article published in December 2004

Impact of rituximab on immunoglobulin concentrations and B cell numbers after cyclophosphamide treatment in patients with ANCA-associated vasculitides

scientific article

Inflammatory bowel disease and mutations affecting the interleukin-10 receptor

scientific article

Long-lived plasma cells and memory B cells produce pathogenic anti-GAD65 autoantibodies in Stiff Person Syndrome

scientific article

MiR-146a regulates the TRAF6/TNF-axis in donor T cells during GVHD.

scientific article published on 9 September 2014

Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects

scientific article published on 04 May 2018

Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency

scientific article

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

scientific article

Reversible pancytopenia and immunodeficiency in a patient with hereditary folate malabsorption

scientific article

Rituximab as Induction Therapy in Eosinophilic Granulomatosis with Polyangiitis Refractory to Conventional Immunosuppressive Treatment: A 36-Month Follow-Up Analysis.

scientific article

Rituximab in the treatment of refractory or relapsing eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome).

scientific article published on 24 September 2013

Screening of functional and positional candidate genes in families with common variable immunodeficiency

scientific article

Sequence Analysis of TNFRSF13b, Encoding TACI, in Patients with Systemic Lupus Erythematosus

scientific article published on 27 April 2007

Sequence analysis of BIRC4/XIAP in male patients with common variable immunodeficiency

scientific article published on 03 June 2008

Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis.

scientific article published on 26 March 2014

T and B lymphocyte abnormalities in bone marrow biopsies of common variable immunodeficiency.

scientific article published on 16 May 2011

The MRZ reaction helps to distinguish rheumatologic disorders with central nervous involvement from multiple sclerosis.

scientific article published on 31 January 2018

The role of HLA DQ2 and DQ8 in dissecting celiac-like disease in common variable immunodeficiency.

scientific article published on 23 April 2013

The serum heavy/light chain immunoassay: A valuable tool for sensitive paraprotein assessment, risk, and disease monitoring in monoclonal gammopathies.

scientific article published on 8 September 2017

[Primary Immunodeficiency in Adults]

scientific article published on 31 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 Ulrich Salzer

A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency.

A feeder-free differentiation system identifies autonomously proliferating B cell precursors in human bone marrow

A homozygous CARD9 mutation in a family with susceptibility to fungal infections

A novel disease-causing synonymous exonic mutation in GATA2 affecting RNA splicing

A syndrome with congenital neutropenia and mutations in G6PC3

Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells

Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations

B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans.

B-cell signaling in persistent polyclonal B lymphocytosis (PPBL).

BAFF- and TACI-Dependent Processing of BAFFR by ADAM Proteases Regulates the Survival of B Cells

Cast Nephropathy and Deceptively Low Absolute Serum Free Light Chain Levels: Resolution of a Challenging Case and Systematic Review of the Literature

Circulating CD21low B cells in common variable immunodeficiency resemble tissue homing, innate-like B cells.

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

Common variable immunodeficiency - an update ⬇️

Common variable immunodeficiency at the end of a prospering decade: towards novel gene defects and beyond ⬇️

Common variable immunodeficiency: The power of co-stimulation.

Common variable immunodeficiency: a multifaceted and puzzling disorder

DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency.

Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity

Diffuse parenchymal lung disease as first clinical manifestation of GATA-2 deficiency in childhood.

Fatal adult-onset antibody deficiency syndrome in a patient with cartilage hair hypoplasia

Gray platelet syndrome can mimic autoimmune lymphoproliferative syndrome

Heterozygous alterations of TNFRSF13B/TACI in tonsillar hypertrophy and sarcoidosis.

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

Human ICOS deficiency abrogates the germinal center reaction and provides a monogenic model for common variable immunodeficiency

ICOS deficiency in patients with common variable immunodeficiency.

Impact of rituximab on immunoglobulin concentrations and B cell numbers after cyclophosphamide treatment in patients with ANCA-associated vasculitides

Inflammatory bowel disease and mutations affecting the interleukin-10 receptor

Long-lived plasma cells and memory B cells produce pathogenic anti-GAD65 autoantibodies in Stiff Person Syndrome

MiR-146a regulates the TRAF6/TNF-axis in donor T cells during GVHD.

Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects

Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

Reversible pancytopenia and immunodeficiency in a patient with hereditary folate malabsorption

Rituximab as Induction Therapy in Eosinophilic Granulomatosis with Polyangiitis Refractory to Conventional Immunosuppressive Treatment: A 36-Month Follow-Up Analysis.

Rituximab in the treatment of refractory or relapsing eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome).

Screening of functional and positional candidate genes in families with common variable immunodeficiency

Sequence Analysis of TNFRSF13b, Encoding TACI, in Patients with Systemic Lupus Erythematosus

Sequence analysis of BIRC4/XIAP in male patients with common variable immunodeficiency

Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis.

T and B lymphocyte abnormalities in bone marrow biopsies of common variable immunodeficiency.

The MRZ reaction helps to distinguish rheumatologic disorders with central nervous involvement from multiple sclerosis.

The role of HLA DQ2 and DQ8 in dissecting celiac-like disease in common variable immunodeficiency.

The serum heavy/light chain immunoassay: A valuable tool for sensitive paraprotein assessment, risk, and disease monitoring in monoclonal gammopathies.

[Primary Immunodeficiency in Adults]

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