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Current perspectives on primary immunodeficiency diseases
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scholarly article
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review article
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stated in
PubMed
retrieved
30 June 2019
title
Current perspectives on primary immunodeficiency diseases
(English)
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main subject
autoimmune disease
1 reference
stated in
PubMed
retrieved
30 June 2019
immunodeficiency
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stated in
PubMed
retrieved
30 June 2019
author
M. Eric Gershwin
series ordinal
3
object named as
M Eric Gershwin
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author name string
Arvind Kumar
series ordinal
1
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Suzanne S Teuber
series ordinal
2
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language of work or name
English
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publication date
2006
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stated in
PubMed
published in
Clinical and Developmental Immunology
1 reference
stated in
PubMed Central
retrieved
30 June 2019
volume
13
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issue
2-4
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page(s)
223-59
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copyright license
Creative Commons Attribution
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PubMed Central
retrieved
30 June 2019
copyright status
copyrighted
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ScienceSource
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cites work
Severe congenital leukopenia (reticular dysgenesis). Immunologic and morphologic characterizations of leukocytes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Bruton's tyrosine kinase gene is expressed throughout B cell differentiation, from early precursor B cell stages preceding immunoglobulin gene rearrangement up to mature B cell stages
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies)
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The presentation and natural history of immunodeficiency caused by nuclear factor kappaB essential modulator mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human nuclear factor kappa B essential modulator mutation can result in immunodeficiency without ectodermal dysplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Purine nucleoside phosphorylase deficiency (PNP-def) presenting with lymphopenia and developmental delay: successful correction with umbilical cord blood transplantation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Subnormal serum concentrations of IgG2 in children with frequent infections associated with varied patterns of immunologic dysfunction.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Treatment options for genetically determined immunodeficiency
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CD40 ligand mutations in X-linked immunodeficiency with hyper-IgM
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Anaphylactic reactions after gamma globulin administration in patients with hypogammaglobulinemia. Detection of IgE antibodies to IgA
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
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Complement. First of two parts
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Crossref
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https://api.crossref.org/works/10.1080%2F17402520600800705
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7 January 2021
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Complement. Second of two parts
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Crossref
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https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
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The clinical, immunological, and molecular spectrum of chromosome 22q11.2 deletion syndrome and DiGeorge syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A subject with a novel type I bare lymphocyte syndrome has tapasin deficiency due to deletion of 4 exons by Alu-mediated recombination
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B-severe combined immune deficiency or Omenn syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A case of invasive aspergillosis in CGD patient successfully treated with Amphotericin B and INF-gamma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical and immunologic characteristics of healthy children with subnormal serum concentrations of IgG2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1080%2F17402520600800705
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1080/17402520600800705
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PMC publication ID
2270780
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PubMed publication ID
17162365
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ResearchGate publication ID
6638127
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