Educational paper: primary antibody deficiencies (Q28236790)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

CD20 deficiency in humans results in impaired T cell-independent antibody responses

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Primary immunodeficiencies: 2009 update

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

TACI is mutant in common variable immunodeficiency and IgA deficiency

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Transient hypogammaglobulinemia of infancy presenting as Staphylococcus aureus sepsis with deep neck infection

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2)

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

The European internet-based patient and research database for primary immunodeficiencies: results 2006-2008

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Educational paper: syndromic forms of primary immunodeficiency

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Infants aged 12 months can mount adequate serotype-specific IgG responses to pneumococcal polysaccharide vaccine

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

The HDAC inhibitor panobinostat (LBH589) inhibits mesothelioma and lung cancer cells in vitro and in vivo with particular efficacy for small cell lung cancer

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Growth hormone deficiency and antipituitary antibodies in a patient with common variable immunodeficiency

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Molecular diagnostics of primary immunodeficiencies: benefits and future challenges

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Common variable immunodeficiency disorders in children: delayed diagnosis despite typical clinical presentation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Low level IGF-1 and common variable immune deficiency: an unusual combination.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Human PMS2 deficiency is associated with impaired immunoglobulin class switch recombination

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Memory B cells in common variable immunodeficiency: clinical associations and sex differences

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

A regulatory role for NBS1 in strand-specific mutagenesis during somatic hypermutation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Autoimmunity in IgA deficiency: revisiting the role of IgA as a silent housekeeper

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Gastrointestinal tract pathology in patients with common variable immunodeficiency (CVID): a clinicopathologic study and review

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

TACI mutation in common variable immunodeficiency and IgA deficiency

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Specific NEMO mutations impair CD40-mediated c-Rel activation and B cell terminal differentiation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Common variable immune deficiency: respiratory manifestations, pulmonary function and high-resolution CT scan findings

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Physiology of IgA and IgA deficiency

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

The comparison of the efficacy and safety of intravenous versus subcutaneous immunoglobulin replacement therapy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Selective IgA deficiency in Japanese blood donors: frequency and statistical analysis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Laboratory diagnosis of specific antibody deficiency to pneumococcal capsular polysaccharide antigens by multiplexed bead assay

2 June 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

The loss of IgM memory B cells correlates with clinical disease in common variable immunodeficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

Common variable immunodeficiency disorders: division into distinct clinical phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

Common variable immunodeficiency: clinical and immunological features of 248 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

The outcome of patients with hypogammaglobulinemia in infancy and early childhood

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

IgA deficiency: clinical correlates and responses to pneumococcal vaccine

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

Quality of life and health-care resource utilization among children with primary immunodeficiency receiving home treatment with subcutaneous human immunoglobulin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

Laboratory diagnosis of specific antibody deficiency to pneumococcal capsular polysaccharide antigens

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

Clinical spectrum of X-linked hyper-IgM syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

Infection outcomes in patients with common variable immunodeficiency disorders: relationship to immunoglobulin therapy over 22 years.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

TACI mutations and disease susceptibility in patients with common variable immunodeficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

Timing of antiretroviral therapy initiation in tuberculosis patients with AIDS: a decision analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

The four most common pediatric immunodeficiencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

Lymphocyte characteristics in children with common variable immunodeficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

The EUROclass trial: defining subgroups in common variable immunodeficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

The X-linked hyper-IgM syndrome: clinical and immunologic features of 79 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

Mannose Binding Lectin Polymorphisms are Associated With Early Age of Disease Onset and Autoimmunity in Common Variable Immunodeficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1474-X

Pediatric common variable immunodeficiency: immunologic and phenotypic associations with switched memory B cells.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Response to polysaccharide vaccination amongst pediatric patients with common variable immunodeficiency correlates with clinical disease

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

A prospective study on children with initial diagnosis of transient hypogammaglobulinemia of infancy: results from the Italian Primary Immunodeficiency Network.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

Analysis of class-switched memory B cells in patients with common variable immunodeficiency and its clinical implications.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

CD40 Ligand Gene Defects Responsible for X-Linked Hyper-IgM Syndrome

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3098982

[Molecular diagnosis of primary immunodeficiencies]

27 November 2018

1 reference

12 December 2020

Long-term follow-up and outcome of a large cohort of patients with common variable immunodeficiency

1 reference

12 December 2020

Two relapses of group B streptococcal sepsis and transient hypogammaglobulinemia

1 reference

12 December 2020

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

1 reference

12 December 2020

Development of a common variable immunodeficiency in IgA-deficient patients

1 reference

12 December 2020

Primary care physicians and their HIV prevention practices

1 reference

12 December 2020

A CT scan score for the assessment of lung disease in children with common variable immunodeficiency disorders

1 reference

12 December 2020

Age- and serotype-dependent antibody response to pneumococcal polysaccharides

1 reference

12 December 2020

X-linked agammaglobulinemia: report on a United States registry of 201 patients

1 reference

12 December 2020

10.1007/S00431-011-1474-X

Identifiers

DOI

1 reference

Dimensions Publication ID

1018477464

0 references

1 reference

1 reference

PubMed publication ID

21544519

1 reference