(Q35867518)

10 August 2017

1 reference

title

Development of granulomatous common variable immunodeficiency subsequent to infection with Toxoplasma gondii (English)

1 reference

common variable immunodeficiency

10 August 2017

0 references

1 reference

5

1 reference

10 August 2017

S Mrusek

1

1 reference

10 August 2017

A Marx

2

1 reference

10 August 2017

J Kummerle-Deschner

3

1 reference

10 August 2017

N Tzaribachev

4

1 reference

10 August 2017

U-N Riede

6

1 reference

10 August 2017

K Warnatz

7

1 reference

10 August 2017

G E Dannecker

8

1 reference

10 August 2017

S Ehl

9

1 reference

10 August 2017

language of work or name

1 reference

1 September 2004

1 reference

Clinical and Experimental Immunology

10 August 2017

published in

1 reference

10 August 2017

volume

137

1 reference

10 August 2017

issue

3

1 reference

10 August 2017

page(s)

578-583

1 reference

Human genetic defects in class-switch recombination (hyper-IgM syndromes).

10 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2249.2004.02558.X

Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2249.2004.02558.X

Fine mapping of IGAD1 in IgA deficiency and common variable immunodeficiency: identification and characterization of haplotypes shared by affected members of 101 multiple-case families

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2249.2004.02558.X

Common variable immunodeficiency: how many diseases?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2249.2004.02558.X

Sarcoidosis and common variable immunodeficiency. Report of 8 cases and review of the literature.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2249.2004.02558.X

Reversible monoclonal lymphadenopathy in autoimmune lymphoproliferative syndrome with functional FAS (CD95/APO-1) deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2249.2004.02558.X

Noncaseating granulomatous disease in common variable immunodeficiency

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1809154

Granulomatous disease in common variable immunodeficiency: effect on immunoglobulin replacement therapy and response to steroids and splenectomy

14 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1809154

Sarcoidosis associated with combined immunodeficiency

14 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1809154

Toxoplasmosis in a patient with common variable immunodeficiency.

14 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1809154

Characterization of common variable immunodeficiency: identification of a subset of patients with distinctive immunophenotypic and clinical features

14 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1809154

Familial combined cellular and humoral immune defect with multisystem granulomata

14 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1809154

Adult severe combined immunodeficiency and sarcoid-like granulomas with hypersplenism

14 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1809154

The simultaneous presentation of sarcoidosis and common variable immune deficiency

14 November 2018

1 reference

12 December 2020

Alterations of the X-linked lymphoproliferative disease gene SH2D1A in common variable immunodeficiency syndrome

1 reference

12 December 2020

Severe deficiency of switched memory B cells (CD27(+)IgM(-)IgD(-)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease

1 reference

12 December 2020

Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency

1 reference

12 December 2020

Persistent activation of the tumor necrosis factor system in a subgroup of patients with common variable immunodeficiency--possible immunologic and clinical consequences

1 reference

12 December 2020

Granulomatous disease in common variable immunodeficiency

1 reference

12 December 2020

TNF and lymphotoxin-alpha polymorphisms associated with common variable immunodeficiency: role in the pathogenesis of granulomatous disease

1 reference

12 December 2020

Sarcoidosis and common variable immunodeficiency. A case of a malignant course of sarcoidosis in conjunction with severe impairment of the cellular and humoral immune system

1 reference

12 December 2020

10.1111/J.1365-2249.2004.02558.X

Identifiers

DOI

1 reference

10 August 2017

0 references

1 reference