(Q37980033)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22290360%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

title

Autoimmune Addison disease: pathophysiology and genetic complexity (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22290360%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22290360%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Simon Pearce

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22290360%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

author name string

Anna L Mitchell

series ordinal

1

1 reference

26 August 2017

Simon H S Pearce

series ordinal

2

1 reference

26 August 2017

publication date

31 January 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22290360%20AND%20SRC:MED&resulttype=core&format=json

Nature Reviews Endocrinology

21 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22290360%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22290360%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22290360%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

page(s)

306-316

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22290360%20AND%20SRC:MED&resulttype=core&format=json

Eighty-six cases of Addison's disease

21 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

High prevalence and increasing incidence of Addison's disease in western Norway

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Associated autoimmunity in Addison's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Genetic dissection of complex traits

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

21-Hydroxylase, a major autoantigen in idiopathic Addison's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Mechanism of inhibition of cytochrome P450 C21 enzyme activity by autoantibodies from patients with Addison's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Identification by molecular cloning of an autoantigen associated with Addison's disease as steroid 17 alpha-hydroxylase

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Two different cytochrome P450 enzymes are the adrenal antigens in autoimmune polyendocrine syndrome type I and Addison's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

The natural history of adrenal function in autoimmune patients with adrenal autoantibodies

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Estimated risk for developing autoimmune Addison's disease in patients with adrenal cortex autoantibodies

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Long-lasting subclinical Addison's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Partial recovery of adrenal function in a patient with autoimmune Addison's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Positional cloning of the APECED gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Autoimmune polyendocrinopathy syndrome type 1: treat with kid gloves

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Polyglandular autoimmune syndrome type I among Iranian Jews

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Autoimmune polyendocrine syndrome type 1 in Norway: phenotypic variation, autoantibodies, and novel mutations in the autoimmune regulator gene.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Two types of autoimmune Addison's disease associated with different polyglandular autoimmune (PGA) syndromes.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Clinical review 93: Autoimmune polyglandular syndrome type 1.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

The role of AIRE in human autoimmune disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Polyglandular autoimmune syndromes: immunogenetics and long-term follow-up

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Autoimmune adrenocortical failure in Norway autoantibodies and human leukocyte antigen class II associations related to clinical features

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Hypoadrenocorticism in small animals

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Heritability and complex segregation analysis of hypoadrenocorticism in the standard poodle

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Inheritance of hypoadrenocorticism in bearded collies

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

A review of immunologic diseases of the dog.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Hypoadrenocorticism in a family of leonbergers

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Understanding the genetics of autoimmune disease: two loci that regulate late onset Addison's disease in Portuguese Water Dogs

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Association of a dog leukocyte antigen class II haplotype with hypoadrenocorticism in Nova Scotia Duck Tolling Retrievers

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Addison's disease in identical twins.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Auto-immune Addison's disease in identical twins

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

ADDISON'S DISEASE IN IDENTICAL TWINS

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Autoimmune Addison's disease and thyrotoxic thyroiditis presenting as encephalopathy in twins

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Immunoregulation abnormalities in familial Addison's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Addison's disease occurring in sisters

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Genetic analysis of autoimmune disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

The genetics of autoimmune thyroid disease.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Familial association between type 1 diabetes and other autoimmune and related diseases

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Inherited susceptibility to autoimmune Addison's disease is linked to human leukocyte antigens-DR3 and/or DR4, except when associated with type I autoimmune polyglandular syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

The HLA-DQ beta non-Asp-57 allele: a predictor of future insulin-dependent diabetes mellitus in patients with autoimmune Addison's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Major histocompatibility complex class II and III in Addison's disease. MHC alleles do not predict autoantibody specificity and 21-hydroxylase gene polymorphism has no independent role in disease susceptibility

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Additional association of intra-MHC genes, MICA and D6S273, with Addison's disease.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Steroid 21-hydroxylase gene polymorphism in Addison's disease patients

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Homozygosity of the polymorphism MICA5.1 identifies extreme risk of progression to overt adrenal insufficiency among 21-hydroxylase antibody-positive patients with type 1 diabetes.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Three novel mutations of the CIITA gene in MHC class II-deficient patients with a severe immunodeficiency

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Single nucleotide polymorphisms in the gene encoding the major histocompatibility complex class II transactivator (CIITA) in systemic lupus erythematosus

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Investigation of the MHC2TA gene, associated with rheumatoid arthritis in a Swedish population, in a UK rheumatoid arthritis cohort

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

MHC2TA single nucleotide polymorphism and genetic risk for autoimmune adrenal insufficiency

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

A new member of the immunoglobulin superfamily--CTLA-4

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Association of autoimmune thyroid disease with microsatellite markers for the thyrotropin receptor gene and CTLA-4 in Japanese patients

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

A CTLA-4 gene polymorphism is associated with both Graves disease and autoimmune hypothyroidism.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Insulin-dependent diabetes mellitus (IDDM) is associated with CTLA4 polymorphisms in multiple ethnic groups

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry

31 March 2020

2 references

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

31 March 2020

12 December 2020

CTLA4 codon 17 dimorphism in patients with rheumatoid arthritis

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

An association between the CTLA4 exon 1 polymorphism and early rheumatoid arthritis with autoimmune endocrinopathies

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patients

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

The soluble CTLA-4 splice variant protects from type 1 diabetes and potentiates regulatory T-cell function

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Soluble CTLA-4 receptor an immunological marker of Graves' disease and severity of ophthalmopathy is associated with CTLA-4 Jo31 and CT60 gene polymorphisms

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Cutting edge: a soluble form of CTLA-4 in patients with autoimmune thyroid disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Sex-specific association of PTPN22 1858T with type 1 diabetes but not with Hashimoto's thyroiditis or Addison's disease in the German population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Genetic variation in PTPN22 corresponds to altered function of T and B lymphocytes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Cutting edge: the PTPN22 allelic variant associated with autoimmunity impairs B cell signaling

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

The autoimmune disease-associated PTPN22 variant promotes calpain-mediated Lyp/Pep degradation associated with lymphocyte and dendritic cell hyperresponsiveness.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Blockade of programmed death-1 ligands on dendritic cells enhances T cell activation and cytokine production

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Association of an A/C single nucleotide polymorphism in programmed cell death-ligand 1 gene with Graves' disease in Japanese patients

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibility

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Fine Mapping of the PSORS4 Psoriasis Susceptibility Region on Chromosome 1q21

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Fcgamma receptor gene polymorphisms in Japanese patients with systemic lupus erythematosus: contribution of FCGR2B to genetic susceptibility

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Fc receptor-like proteins (FCRL): immunomodulators of B cell function

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease association

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Genetic variations in NALP1 are associated with generalized vitiligo in a Romanian population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

A coding variant in NLRP1 is associated with autoimmune Addison's disease.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Variation within the CLEC16A gene shows consistent disease association with both multiple sclerosis and type 1 diabetes in Sardinia.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Multiple common variants for celiac disease influencing immune gene expression

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15(-) Crohn's disease patients

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Prevention of autoimmune diabetes in NOD mice by 1,25 dihydroxyvitamin D3

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Vitamin D and autoimmune diabetes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

A promoter polymorphism of the CYP27B1 gene is associated with Addison's disease, Hashimoto's thyroiditis, Graves' disease and type 1 diabetes mellitus in Germans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

A haplotype of the CYP27B1 promoter is associated with autoimmune Addison's disease but not with Graves' disease in a UK population

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Autoimmune adrenal insufficiency and autoimmune polyendocrine syndromes: autoantibodies, autoantigens, and their applicability in diagnosis and disease prediction

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Intraadrenal steroid concentrations in man: zonal differences and developmental changes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Glucocorticoids severely impair differentiation and antigen presenting function of dendritic cells despite upregulation of Toll-like receptors.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Inhibition of Th1 immune response by glucocorticoids: dexamethasone selectively inhibits IL-12-induced Stat4 phosphorylation in T lymphocytes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Dexamethasone preferentially suppresses plasmacytoid dendritic cell differentiation and enhances their apoptotic death

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Glucocorticoids down‐regulate dendritic cell function in vitro and in vivo

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Genetic variant of the scavenger receptor BI in humans

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Analysis of extended human leukocyte antigen haplotype association with Addison's disease in three populations

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Multiple loci in the HLA complex are associated with Addison's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Vitamin D receptor genotype is associated with Addison's disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRENDO.2011.245

Although DR3-DQB1*0201 may be associated with multiple component diseases of the autoimmune polyglandular syndromes, the human leukocyte antigen DR4-DQB1*0302 haplotype is implicated only in beta-cell autoimmunity

31 March 2020

1 reference

12 December 2020

Pretreatment clinical and laboratory findings in dogs with hypoadrenocorticism: 225 cases (1979-1993).

1 reference

12 December 2020

Focal lymphocytic infiltration in the adrenal cortex of the elderly: immunohistological analysis of infiltrating lymphocytes

1 reference

12 December 2020

The genetics of NOD-like receptors in Crohn's disease

1 reference

12 December 2020

Microsatellite polymorphism of the MHC class I chain-related (MIC-A and MIC-B) genes marks the risk for autoimmune Addison's disease

1 reference

12 December 2020

Association analysis of the cytotoxic T lymphocyte antigen-4 (CTLA-4) and autoimmune regulator-1 (AIRE-1) genes in sporadic autoimmune Addison's disease

1 reference

12 December 2020

IL-4 and IL-2 selectively rescue Th cell subsets from glucocorticoid-induced apoptosis

1 reference

12 December 2020

Remission of subclinical adrenocortical failure in subjects with adrenal autoantibodies

1 reference

12 December 2020

Hormonal responses during various phases of autoimmune adrenal failure: no evidence for 21-hydroxylase enzyme activity inhibition in vivo

1 reference

12 December 2020

Time course of 21-hydroxylase antibodies and long-term remission of subclinical autoimmune adrenalitis after corticosteroid therapy: case report

1 reference

12 December 2020

Association of autoimmune thyroid disease with a microsatellite marker for the thyrotropin receptor gene and CTLA-4 in a Japanese population.

1 reference

12 December 2020

DRB1*04 and DQ alleles: expression of 21-hydroxylase autoantibodies and risk of progression to Addison's disease

1 reference

12 December 2020

Type 2 polyglandular autoimmune disease (Schmidt's syndrome).

1 reference

12 December 2020

Genetic evaluation of Addison's disease in the Portuguese Water Dog

1 reference

12 December 2020

Is the prevalence of Addison's disease underestimated?

1 reference

12 December 2020

Autoimmune Addison's disease--evidence for a role of steroid 21-hydroxylase autoantibodies in adrenal insufficiency

1 reference

12 December 2020

The biochemistry and molecular biology of glucocorticoid-induced apoptosis in the immune system.

1 reference

12 December 2020

Addison's disease - a review of some clinical, pathological and immunological features.

1 reference

12 December 2020

Assessing the role of HLA-linked and unlinked determinants of disease

1 reference

12 December 2020

Clinical review 130: Addison's disease 2001.

1 reference

12 December 2020

CTLA-4 gene polymorphism associated with Graves' disease in a Caucasian population.

1 reference

12 December 2020

A polymorphism within the vitamin D-binding protein gene is associated with Graves' disease but not with Hashimoto's thyroiditis

1 reference

12 December 2020

Adrenal autoantibodies and organ-specific autoimmunity in patients with Addison's disease

1 reference

12 December 2020

A conformation-dependent epitope in Addison's disease and other endocrinological autoimmune diseases maps to a carboxyl-terminal functional domain of human steroid 21-hydroxylase

1 reference

12 December 2020

Identifiers

DOI

10.1038/NRENDO.2011.245

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22290360%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

1 reference