Autoimmune polyendocrine syndrome type 1 - model disease for autoimmunity
- Prosjektnummer
- 911303
- Ansvarlig person
- Eystein S. Husebye
- Institusjon
- Universitetet i Bergen
- Prosjektkategori
- Forskningsprosjekt
- Helsekategori
- Endocrinology & Metabolism
- Forskningsaktivitet
- Translasjonsforskning
Normal overall mortality rate in Addison's disease, but young patients are at risk of premature death.
Eur J Endocrinol 2009 Feb;160(2):233-7. Epub 2008 nov 14
PMID: 19011006
A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes.
Genes Immun 2009 Mar;10(2):120-4. Epub 2008 okt 23
PMID: 18946481
Autoantibodies against type I interferons as an additional diagnostic criterion for autoimmune polyendocrine syndrome type I.
J Clin Endocrinol Metab 2008 Nov;93(11):4389-97. Epub 2008 aug 26
PMID: 18728167
Radioimmunoassay for autoantibodies against interferon omega; its use in the diagnosis of autoimmune polyendocrine syndrome type I.
Clin Immunol 2008 Oct;129(1):163-9. Epub 2008 aug 16
PMID: 18708298
Interferon autoantibodies associated with AIRE deficiency decrease the expression of IFN-stimulated genes.
Blood 2008 Oct;112(7):2657-66. Epub 2008 jul 7
PMID: 18606876
Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency.
J Clin Endocrinol Metab 2008 Sep;93(9):3310-7. Epub 2008 jul 1
PMID: 18593762
Autoimmune polyendocrine syndrome type I in Slovakia: relevance of screening patients with autoimmune Addison's disease.
Eur J Endocrinol 2008 May;158(5):705-9.
PMID: 18426830
Microarray analysis reveals down-regulation of the tumour suppressor gene WWOX and up-regulation of the oncogene TYMS in intracranial sporadic meningiomas.
J Neurooncol 2008 Jul;88(3):251-9. Epub 2008 mar 26
PMID: 18365142
Replacement therapy for Addison's disease: recent developments.
Expert Opin Investig Drugs 2008 Apr;17(4):497-509.
PMID: 18363515
[Endocrinologic emergency medicine]
Tidsskr Nor Laegeforen 2008 Feb;128(5):574.
PMID: 18333289
Autoimmune polyendocrine syndrome type 1 and NALP5, a parathyroid autoantigen.
N Engl J Med 2008 Mar;358(10):1018-28.
PMID: 18322283
Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease.
Eur J Hum Genet 2008 Aug;16(8):977-82. Epub 2008 feb 27
PMID: 18301444
AIRE variations in Addison's disease and autoimmune polyendocrine syndromes (APS): partial gene deletions contribute to APS I.
Genes Immun 2008 Mar;9(2):130-6. Epub 2008 jan 17
PMID: 18200029
Epitope mapping of human aromatic L-amino acid decarboxylase.
Biochem Biophys Res Commun 2007 Feb;353(3):692-8. Epub 2006 des 22
PMID: 17194446
Autoimmune polyendocrine syndrome type 1 in Norway: phenotypic variation, autoantibodies, and novel mutations in the autoimmune regulator gene.
J Clin Endocrinol Metab 2007 Feb;92(2):595-603. Epub 2006 nov 21
PMID: 17118990
Pituitary autoantibodies in autoimmune polyendocrine syndrome type 1.
Proc Natl Acad Sci U S A 2007 Jan;104(3):949-54. Epub 2007 jan 10
PMID: 17215373
Anti-interferon autoantibodies in autoimmune polyendocrinopathy syndrome type 1.
PLoS Med 2006 Jul;3(7):e289.
PMID: 16784312
eRapport er utarbeidet av Sølvi Lerfald og Reidar Thorstensen, Regionalt kompetansesenter for klinisk forskning, Helse Vest RHF, og videreutvikles av de fire RHF-ene i fellesskap, med støtte fra Helse Vest IKT
Alle henvendelser rettes til Faglig rapportering, Helse Vest