(Q53030760)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18051214%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

title

Analysis of genetic defects in patients with the common variable immunodeficiency phenotype in a single Taiwanese tertiary care hospital (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18051214%20AND%20SRC:MED&resulttype=core&format=json

common variable immunodeficiency

28 December 2019

main subject

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18051214%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

author name string

Wen-I Lee

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18051214%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Ming-Ling Kuo

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18051214%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Syh-Jae Lin

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18051214%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Li-Chen Chen

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18051214%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Mai-Tzu Chen

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18051214%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Tang-Her Jaing

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18051214%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

publication date

1 November 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18051214%20AND%20SRC:MED&resulttype=core&format=json

Annals of Allergy, Asthma & Immunology

28 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18051214%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

volume

99

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18051214%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

issue

5

1 reference

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28 December 2019

page(s)

433-442

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18051214%20AND%20SRC:MED&resulttype=core&format=json

Tackling the heterogeneity of CVID.

28 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies)

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

X-linked agammaglobulinemia. A clinical and molecular analysis

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Clinical and mutational characteristics of X-linked agammaglobulinemia and its carrier identified by flow cytometric assessment combined with genetic analysis

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Extreme variation in X-linked agammaglobulinemia phenotype in a three-generation family

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Phenotypic variability: clinical presentation between the 6th year and the 60th year in a family with X-linked agammaglobulinemia

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

A case of X-linked agammaglobulinemia diagnosed in adulthood

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinaemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency Registry

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Parvovirus B19-induced anemia as the presenting manifestation of X-linked hyper-IgM syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Molecular analysis of a large cohort of patients with the hyper immunoglobulin M (IgM) syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

X-linked lymphoproliferative disease: three atypical cases

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

ICOS is an inducible T-cell co-stimulator structurally and functionally related to CD28

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Differential expression of inducible costimulator-ligand splice variants: lymphoid regulation of mouse GL50-B and human GL50 molecules

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

ICOS deficiency in patients with common variable immunodeficiency.

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

TACI and BAFF-R mediate isotype switching in B cells

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

TACI is mutant in common variable immunodeficiency and IgA deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

TACItly changing tunes: farewell to a yin and yang of BAFF receptor and TACI in humoral immunity? New genetic defects in common variable immunodeficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

An antibody-deficiency syndrome due to mutations in the CD19 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Primary immunodeficiency diseases consortium conference

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Distribution and clinical aspects of primary immunodeficiencies in a Taiwan pediatric tertiary hospital during a 20-year period.

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Bruton's tyrosine kinase is present in normal platelets and its absence identifies patients with X-linked agammaglobulinaemia and carrier females

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Inducible CO-stimulator molecule, a candidate gene for defective isotype switching, is normal in patients with hyper-IgM syndrome of unknown molecular diagnosis.

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Mutational Analysis of Human BAFF Receptor TNFRSF13C (BAFF-R) in Patients with Common Variable Immunodeficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

The protein kinase family: conserved features and deduced phylogeny of the catalytic domains

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

BTKbase, mutation database for X-linked agammaglobulinemia (XLA)

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

CD40 ligand gene defects responsible for X-linked hyper-IgM syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

CD40 ligand mutations in X-linked immunodeficiency with hyper-IgM

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Defective expression of the CD40 ligand in X chromosome-linked immunoglobulin deficiency with normal or elevated IgM

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Defective expression of T-cell CD40 ligand causes X-linked immunodeficiency with hyper-IgM

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Immunoglobulin class and subclass deficiencies prior to Epstein-Barr virus infection in males with X-linked lymphoproliferative disease

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

Recurrent B-cell non-Hodgkin's lymphoma in two brothers with X-linked lymphoproliferative disease without evidence for Epstein-Barr virus infection

1 reference

https://api.crossref.org/works/10.1016%2FS1081-1206%2810%2960569-8

7 January 2021

10.1016/S1081-1206(10)60569-8

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18051214%20AND%20SRC:MED&resulttype=core&format=json

release_jsetydug5rfc7k3gkrajgqrpje

28 December 2019

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jsetydug5rfc7k3gkrajgqrpje

24 November 2022

mapped directly with Wikidata item

1 reference