(Q34445745)

2 August 2017

5 references

12 March 2019

13 March 2019

24 March 2019

17 June 2019

30 June 2019

0 references

Cutaneous vasculitis in patients with autoimmune polyendocrine syndrome type 1: report of a case and brief review of the literature (English)

1 reference

autoimmune polyendocrine syndrome type 1

2 August 2017

main subject

0 references

autoimmune polyendocrine syndrome

5 references

12 March 2019

13 March 2019

24 March 2019

17 June 2019

30 June 2019

vascular skin disease

5 references

12 March 2019

13 March 2019

24 March 2019

17 June 2019

30 June 2019

5 references

12 March 2019

13 March 2019

24 March 2019

17 June 2019

30 June 2019

6

1 reference

2 August 2017

Emilia Cirillo

3

0 references

author name string

Nicola Improda

1

1 reference

2 August 2017

Donatella Capalbo

2

1 reference

2 August 2017

Manuela Cerbone

4

1 reference

2 August 2017

Andrea Esposito

5

1 reference

2 August 2017

Mariacarolina Salerno

7

1 reference

2 August 2017

language of work or name

1 reference

1 November 2014

6 references

2 August 2017

12 March 2019

13 March 2019

24 March 2019

17 June 2019

30 June 2019

6 references

2 August 2017

12 March 2019

13 March 2019

24 March 2019

17 June 2019

30 June 2019

14

1 reference

2 August 2017

page(s)

272

1 reference

Creative Commons Attribution

2 August 2017

copyright license

5 references

12 March 2019

13 March 2019

24 March 2019

17 June 2019

30 June 2019

0 references

on focus list of Wikimedia project

ScienceSource

0 references

cites work

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy from the pediatric perspective

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4286916

A child with autoimmune polyendocrinopathy candidiasis and ectodermal dysplasia treated with immunosuppression: a case report

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4286916

Genetic basis of altered central tolerance and autoimmune diseases: a lesson from AIRE mutations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4286916

Clinical manifestations and management of patients with autoimmune polyendocrine syndrome type I.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4286916

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4286916

Autoimmune lymphoproliferative syndrome with somatic Fas mutations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4286916

Clinical review 93: Autoimmune polyglandular syndrome type 1.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4286916

Subsepsis allergica in a patient with type I polyglandular autoimmune syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4286916

MONILIASIS, STEATORRHEA, DIABETES MELLITUS, CIRRHOSIS, GALLSTONES, AND HYPOPARATHYROIDISM IN A 10-YEAR-OLD BOY.

6 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2431-14-272

Loss of enteroendocrine cells in autoimmune-polyendocrine-candidiasis-ectodermal-dystrophy (APECED) syndrome with gastrointestinal dysfunction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2431-14-272

Autoantibodies against Type I Interferons as an Additional Diagnostic Criterion for Autoimmune Polyendocrine Syndrome Type I

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2431-14-272

II. Adrenal cortex and steroid 21-hydroxylase autoantibodies in children with organ-specific autoimmune diseases: markers of high progression to clinical Addison's disease.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4286916

Detection of a complete autoimmune regulator gene deletion and two additional novel mutations in a cohort of patients with atypical phenotypic variants of autoimmune polyglandular syndrome type 1

27 October 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2431-14-272

Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2431-14-272

Tryptophan hydroxylase autoantibodies as markers of a distinct autoimmune gastrointestinal component of autoimmune polyendocrine syndrome type 1

21 January 2018

1 reference

12 December 2020

Molecular background and genotype-phenotype correlation in autoimmune-polyendocrinopathy-candidiasis-ectodermal-distrophy patients from Campania and in their relatives.

1 reference

12 December 2020

Erythema annulare centrifugum in a patient with polyglandular autoimmune disease type 1

1 reference

12 December 2020

The natural history of the normal/mild elevated TSH serum levels in children and adolescents with Hashimoto's thyroiditis and isolated hyperthyrotropinaemia: a 3-year follow-up

1 reference

12 December 2020

Chronic Moniliasis Associated with Addison's Disease

1 reference

12 December 2020

High intrafamilial variability in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy: a case study

1 reference

12 December 2020

AIRE mutations and human leukocyte antigen genotypes as determinants of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy phenotype

1 reference

12 December 2020

Lupus-like panniculitis in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)

1 reference

12 December 2020

PERNICIOUS ANEMIA IN A YOUNG GIRL ASSOCIATED WITH IDIOPATHIC HYPOPARATHYROIDISM, FAMILIAL ADDISON'S DISEASE, AND MONILIASIS

1 reference

12 December 2020

[Polyglandular autoimmune syndrome type 1. Different onset forms]

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2431-14-272

1 reference

Dimensions Publication ID

2 August 2017

0 references

1 reference

2 August 2017

1 reference