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Laboratory evaluation of primary immunodeficiencies
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
3412511
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20042230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 January 2020
review article
1 reference
stated in
Europe PubMed Central
title
Laboratory evaluation of primary immunodeficiencies
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
3412511
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20042230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 January 2020
author
Joao B. Oliveira
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
3412511
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20042230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 January 2020
author name string
Thomas A Fleisher
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
3412511
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20042230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 January 2020
language of work or name
English
0 references
publication date
29 December 2009
1 reference
stated in
Europe PubMed Central
PMC publication ID
3412511
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20042230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 January 2020
published in
The Journal of Allergy and Clinical Immunology
1 reference
stated in
Europe PubMed Central
PMC publication ID
3412511
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20042230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 January 2020
volume
125
1 reference
stated in
Europe PubMed Central
PMC publication ID
3412511
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20042230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 January 2020
issue
2 Suppl 2
1 reference
stated in
Europe PubMed Central
PMC publication ID
3412511
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20042230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 January 2020
page(s)
S297-305
1 reference
stated in
Europe PubMed Central
PMC publication ID
3412511
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20042230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 January 2020
cites work
Complement in human diseases: Lessons from complement deficiencies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Primary B cell immunodeficiencies: comparisons and contrasts
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
A rapid flow cytometric screening test for X-linked lymphoproliferative disease due to XIAP deficiency
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
FAS-L, IL-10, and double-negative CD4- CD8- TCR alpha/beta+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Primary immune deficiencies with aberrant IgE production
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
The genetic heterogeneity of mendelian susceptibility to mycobacterial diseases
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Omenn syndrome: inflammation in leaky severe combined immunodeficiency
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Applications of flow cytometry for the study of primary immune deficiencies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Hypogammaglobulinaemia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Hypomorphic nuclear factor-kappaB essential modulator mutation database and reconstitution system identifies phenotypic and immunologic diversity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Pyogenic bacterial infections in humans with MyD88 deficiency
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Revisiting human primary immunodeficiencies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Hemophagocytic lymphohistiocytosis and other hemophagocytic disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Congenital neutropenia syndromes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Primary immune deficiency disorders presenting as autoimmune diseases: IPEX and APECED.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Complement deficiencies and systemic lupus erythematosus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Genetic susceptibility to herpes simplex virus 1 encephalitis in mice and humans
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Immune dysregulation, polyendocrinopathy, enteropathy, X-linked: forkhead box protein 3 mutations and lack of regulatory T cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Inherited human IRAK-4 deficiency: an update.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
STAT3 mutations in the hyper-IgE syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
TLR3 deficiency in patients with herpes simplex encephalitis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Leukocyte adhesion deficiencies: molecular basis, clinical findings, and therapeutic options.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Dominant inhibition of Fas ligand-mediated apoptosis due to a heterozygous mutation associated with autoimmune lymphoproliferative syndrome (ALPS) Type Ib
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Inborn errors of IL-12/23- and IFN-gamma-mediated immunity: molecular, cellular, and clinical features
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Herpes simplex virus encephalitis in human UNC-93B deficiency
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Analysis of natural killer-cell function in familial hemophagocytic lymphohistiocytosis (FHL): defective CD107a surface expression heralds Munc13-4 defect and discriminates between genetic subtypes of the disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Septicemia without sepsis: inherited disorders of nuclear factor-kappa B-mediated inflammation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Development of population-based newborn screening for severe combined immunodeficiency
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Hyper-IgE syndromes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Molecular and cellular pathogenesis of X-linked lymphoproliferative disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Autoimmune lymphoproliferative syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Autoimmune lymphoproliferative syndrome with somatic Fas mutations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Functional and molecular evaluation of lymphocytes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Phagocyte immunodeficiencies and their infections
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Activation-dependent T cell expression of the X-linked lymphoproliferative disease gene product SLAM-associated protein and its assessment for patient detection
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Improved assessment of T-cell receptor (TCR) VB repertoire in clinical specimens: combination of TCR-CDR3 spectratyping with flow cytometry-based TCR VB frequency analysis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Flow cytometric determination of intracytoplasmic Wiskott-Aldrich syndrome protein in peripheral blood lymphocyte subpopulations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a model
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Inherited human Caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome type II
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
A human IFNGR1 small deletion hotspot associated with dominant susceptibility to mycobacterial infection
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 October 2017
Antibody responses to bacteriophage phi X174 in patients with adenosine deaminase deficiency
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
2 July 2018
Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
27 July 2018
Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: an Italian multicenter study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
23 September 2018
The EUROclass trial: defining subgroups in common variable immunodeficiency.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
23 September 2018
Diagnostic paradigm for evaluation of male patients with chronic granulomatous disease, based on the dihydrorhodamine 123 assay
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
23 September 2018
Detection of intracytoplasmic cytokine using flow cytometry and directly conjugated anti-cytokine antibodies.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
23 September 2018
CD40 ligand gene defects responsible for X-linked hyper-IgM syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
23 September 2018
A Fast Procedure for the Detection of Defects in Toll-like Receptor Signaling
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3412511
retrieved
5 December 2018
Transplacentally acquired maternal T lymphocytes in severe combined immunodeficiency: a study of 121 patients
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20042230
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Perforin expression in cytotoxic lymphocytes from patients with hemophagocytic lymphohistiocytosis and their family members
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20042230
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Clinical findings leading to the diagnosis of X-linked agammaglobulinemia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20042230
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Twenty-year follow-up of 160 patients with ataxia-telangiectasia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20042230
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Changes in thymic function with age and during the treatment of HIV infection
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20042230
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Detection of intracellular phosphorylated STAT-1 by flow cytometry
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20042230
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1016/J.JACI.2009.08.043
1 reference
stated in
Europe PubMed Central
PMC publication ID
3412511
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20042230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 January 2020
PMC publication ID
3412511
1 reference
stated in
Europe PubMed Central
PMC publication ID
3412511
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20042230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 January 2020
PubMed publication ID
20042230
1 reference
stated in
Europe PubMed Central
PMC publication ID
3412511
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20042230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
16 January 2020
ResearchGate publication ID
40819216
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