(Q33655443)

English

Increased prevalence of immunoglobulin A deficiency in patients with the chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Increased prevalence of immunoglobulin A deficiency in patients with the chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

immunoglobulin A deficiency

1 reference

based on heuristic

inferred from title

author name string

C A Smith

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

D A Driscoll

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

B S Emanuel

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

D M McDonald-McGinn

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

E H Zackai

5

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

K E Sullivan

6

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

publication date

1 May 1998

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Clinical and Vaccine Immunology

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

415-417

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Humoral immunity in DiGeorge syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=104536

21 June 2018

The association of the DiGeorge anomalad with partial monosomy of chromosome 22.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=104536

21 June 2018

Monosomy 22 with humoral immunodeficiency: is there an immunoglobulin chain deficit?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=104536

21 June 2018

Anaphylactoid transfusion reactions associated with anti-IgA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=104536

21 June 2018

Prediction of persistent immunodeficiency in the DiGeorge anomaly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=104536

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=104536

21 June 2018

A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=104536

21 June 2018

Human serum immunoglobulin concentrations: prevalence of immunoglobulin deficiencies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=104536

21 June 2018

The spectrum of the DiGeorge syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=104536

21 June 2018

Screening of blood donors for IgA deficiency: a study of the donor population of south-west England

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=104536

21 June 2018

Immunophenotyping of blood lymphocytes in childhood. Reference values for lymphocyte subpopulations

1 reference

https://pubmed.ncbi.nlm.nih.gov/9606003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Juvenile rheumatoid arthritis-like polyarthritis in chromosome 22q11.2 deletion syndrome (digeorge anomalad/velocardiofacial syndrome/conotruncal anomaly face syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/9606003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of Correlation between Impaired T Cell Production, Immunodeficiency, and Other Phenotypic Features in Chromosome 22q11.2 Deletion Syndromes (DiGeorge Syndrome/Velocardiofacial Syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/9606003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum levels of immune globulins in health and disease: a survey

1 reference

https://pubmed.ncbi.nlm.nih.gov/9606003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selective IgA deficiency in Australian blood donors

1 reference

https://pubmed.ncbi.nlm.nih.gov/9606003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Large scale detection of IgA deficient blood donors

1 reference

https://pubmed.ncbi.nlm.nih.gov/9606003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selective IgA deficiency in blood donors

1 reference

https://pubmed.ncbi.nlm.nih.gov/9606003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome studies in IgA-deficient patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/9606003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q33655443&oldid=1950575054"