744 related articles for article (PubMed ID: 18616706)
1. Evaluation of the autoimmune regulator (AIRE) gene mutations in a cohort of Italian patients with autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) and in their relatives.
Cervato S; Mariniello B; Lazzarotto F; Morlin L; Zanchetta R; Radetti G; De Luca F; Valenzise M; Giordano R; Rizzo D; Giordano C; Betterle C
Clin Endocrinol (Oxf); 2009 Mar; 70(3):421-8. PubMed ID: 18616706
[TBL] [Abstract][Full Text] [Related]
2. Polymorphisms at +49A/G and CT60 sites in the 3' UTR of the CTLA-4 gene and APECED-related AIRE gene mutations analysis in sporadic idiopathic hypoparathyroidism.
Goswami R; Gupta N; Ray D; Rani R; Tomar N; Sarin R; Vupputuri MR
Int J Immunogenet; 2005 Dec; 32(6):393-400. PubMed ID: 16313305
[TBL] [Abstract][Full Text] [Related]
3. APECED mutations in the autoimmune regulator (AIRE) gene.
Heino M; Peterson P; Kudoh J; Shimizu N; Antonarakis SE; Scott HS; Krohn K
Hum Mutat; 2001 Sep; 18(3):205-11. PubMed ID: 11524731
[TBL] [Abstract][Full Text] [Related]
4. A novel heterozygous mutation of the AIRE gene in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED).
Fierabracci A; Bizzarri C; Palma A; Milillo A; Bellacchio E; Cappa M
Gene; 2012 Dec; 511(1):113-7. PubMed ID: 23000069
[TBL] [Abstract][Full Text] [Related]
5. Dermatological manifestations of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome.
Collins SM; Dominguez M; Ilmarinen T; Costigan C; Irvine AD
Br J Dermatol; 2006 Jun; 154(6):1088-93. PubMed ID: 16704638
[TBL] [Abstract][Full Text] [Related]
6. Novel AIRE mutations and P450 cytochrome autoantibodies in Central and Eastern European patients with APECED.
Cihakova D; Trebusak K; Heino M; Fadeyev V; Tiulpakov A; Battelino T; Tar A; Halász Z; Blümel P; Tawfik S; Krohn K; Lebl J; Peterson P
Hum Mutat; 2001 Sep; 18(3):225-32. PubMed ID: 11524733
[TBL] [Abstract][Full Text] [Related]
7. Autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy in Calabria: clinical, immunological and genetic patterns.
Betterle C; Ghizzoni L; Cassio A; Baronio F; Cervato S; Garelli S; Barbi E; Tonini G
J Endocrinol Invest; 2012 Nov; 35(10):877-81. PubMed ID: 22104652
[TBL] [Abstract][Full Text] [Related]
8. Molecular background of polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome in a Polish population: novel AIRE mutations and an estimate of disease prevalence.
Stolarski B; Pronicka E; Korniszewski L; Pollak A; Kostrzewa G; Rowińska E; Włodarski P; Skórka A; Gremida M; Krajewski P; Ploski R
Clin Genet; 2006 Oct; 70(4):348-54. PubMed ID: 16965330
[TBL] [Abstract][Full Text] [Related]
9. Autoimmune polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) in Sicily: confirmation that R203X is the peculiar AIRE gene mutation.
Giordano C; Modica R; Allotta ML; Guarnotta V; Cervato S; Masiero S; Giordano R; Garelli S; Betterle C
J Endocrinol Invest; 2012 Apr; 35(4):384-8. PubMed ID: 22024611
[TBL] [Abstract][Full Text] [Related]
10. Lupus-like panniculitis in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED).
Füchtenbusch M; Vogel A; Achenbach P; Gummer M; Ziegler AG; Albert E; Standl E; Manns MP
Exp Clin Endocrinol Diabetes; 2003 Aug; 111(5):288-93. PubMed ID: 12951636
[TBL] [Abstract][Full Text] [Related]
11. Analysis of the autoimmune regulator gene in patients with autoimmune non-APECED polyendocrinopathies.
Palma A; Gianchecchi E; Palombi M; Luciano R; Di Carlo P; Crinò A; Cappa M; Fierabracci A
Genomics; 2013 Sep; 102(3):163-8. PubMed ID: 23643663
[TBL] [Abstract][Full Text] [Related]
12. Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different origins.
Scott HS; Heino M; Peterson P; Mittaz L; Lalioti MD; Betterle C; Cohen A; Seri M; Lerone M; Romeo G; Collin P; Salo M; Metcalfe R; Weetman A; Papasavvas MP; Rossier C; Nagamine K; Kudoh J; Shimizu N; Krohn KJ; Antonarakis SE
Mol Endocrinol; 1998 Aug; 12(8):1112-9. PubMed ID: 9717837
[TBL] [Abstract][Full Text] [Related]
13. AIRE mutations and human leukocyte antigen genotypes as determinants of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy phenotype.
Halonen M; Eskelin P; Myhre AG; Perheentupa J; Husebye ES; Kämpe O; Rorsman F; Peltonen L; Ulmanen I; Partanen J
J Clin Endocrinol Metab; 2002 Jun; 87(6):2568-74. PubMed ID: 12050215
[TBL] [Abstract][Full Text] [Related]
14. Autoimmune regulator-1 messenger ribonucleic acid analysis in a novel intronic mutation and two additional novel AIRE gene mutations in a cohort of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients.
Podkrajsek KT; Bratanic N; Krzisnik C; Battelino T
J Clin Endocrinol Metab; 2005 Aug; 90(8):4930-5. PubMed ID: 15886230
[TBL] [Abstract][Full Text] [Related]
15. The genetic background of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy and its autoimmune disease components.
Vogel A; Strassburg CP; Obermayer-Straub P; Brabant G; Manns MP
J Mol Med (Berl); 2002 Apr; 80(4):201-11. PubMed ID: 11976729
[TBL] [Abstract][Full Text] [Related]
16. Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy: report of seven additional sicilian patients and overview of the overall series from sicily.
Valenzise M; Fierabracci A; Cappa M; Porcelli P; Barcellona R; De Luca F; Barollo S; Garelli S; Betterle C
Horm Res Paediatr; 2014; 82(2):127-32. PubMed ID: 25059117
[TBL] [Abstract][Full Text] [Related]
17. Aire deficient mice do not develop the same profile of tissue-specific autoantibodies as APECED patients.
Pöntynen N; Miettinen A; Arstila TP; Kämpe O; Alimohammadi M; Vaarala O; Peltonen L; Ulmanen I
J Autoimmun; 2006 Sep; 27(2):96-104. PubMed ID: 16820279
[TBL] [Abstract][Full Text] [Related]
18. Screening for an AIRE-1 mutation in patients with Addison's disease, type 1 diabetes, Graves' disease and Hashimoto's thyroiditis as well as in APECED syndrome.
Meyer G; Donner H; Herwig J; Böhles H; Usadel KH; Badenhoop K
Clin Endocrinol (Oxf); 2001 Mar; 54(3):335-8. PubMed ID: 11298085
[TBL] [Abstract][Full Text] [Related]
19. Novel and recurrent mutations in the AIRE gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients.
Faiyaz-Ul-Haque M; Bin-Abbas B; Al-Abdullatif A; Abdullah Abalkhail H; Toulimat M; Al-Gazlan S; Almutawa AM; Al-Sagheir A; Peltekova I; Al-Dayel F; Zaidi SH
Clin Genet; 2009 Nov; 76(5):431-40. PubMed ID: 19758376
[TBL] [Abstract][Full Text] [Related]
20. AIRE gene mutations and autoantibodies to interferon omega in patients with chronic hypoparathyroidism without APECED.
Cervato S; Morlin L; Albergoni MP; Masiero S; Greggio N; Meossi C; Chen S; del Pilar Larosa M; Furmaniak J; Rees Smith B; Alimohammadi M; Kämpe O; Valenzise M; Betterle C
Clin Endocrinol (Oxf); 2010 Nov; 73(5):630-6. PubMed ID: 20718774
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
