311 related articles for article (PubMed ID: 22344197)
1. Autoimmune polyendocrine syndrome type 1: an extensive longitudinal study in Sardinian patients.
Meloni A; Willcox N; Meager A; Atzeni M; Wolff AS; Husebye ES; Furcas M; Rosatelli MC; Cao A; Congia M
J Clin Endocrinol Metab; 2012 Apr; 97(4):1114-24. PubMed ID: 22344197
[TBL] [Abstract][Full Text] [Related]
2. Anti-interferon autoantibodies in autoimmune polyendocrinopathy syndrome type 1.
Meager A; Visvalingam K; Peterson P; Möll K; Murumägi A; Krohn K; Eskelin P; Perheentupa J; Husebye E; Kadota Y; Willcox N
PLoS Med; 2006 Jul; 3(7):e289. PubMed ID: 16784312
[TBL] [Abstract][Full Text] [Related]
3. Autoimmune polyendocrine syndrome type 1 in Norway: phenotypic variation, autoantibodies, and novel mutations in the autoimmune regulator gene.
Wolff AS; Erichsen MM; Meager A; Magitta NF; Myhre AG; Bollerslev J; Fougner KJ; Lima K; Knappskog PM; Husebye ES
J Clin Endocrinol Metab; 2007 Feb; 92(2):595-603. PubMed ID: 17118990
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. A Longitudinal Follow-up of Autoimmune Polyendocrine Syndrome Type 1.
Bruserud Ø; Oftedal BE; Landegren N; Erichsen MM; Bratland E; Lima K; Jørgensen AP; Myhre AG; Svartberg J; Fougner KJ; Bakke Å; Nedrebø BG; Mella B; Breivik L; Viken MK; Knappskog PM; Marthinussen MC; Løvås K; Kämpe O; Wolff AB; Husebye ES
J Clin Endocrinol Metab; 2016 Aug; 101(8):2975-83. PubMed ID: 27253668
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Autoimmune polyendocrinopathy-candidosis-ectodermal dystrophy (APECED)--a diagnostic and therapeutic challenge.
Jääskeläinen J; Perheentupa J
Pediatr Endocrinol Rev; 2009 Dec; 7(2):15-28. PubMed ID: 20118890
[TBL] [Abstract][Full Text] [Related]
9. Autoantibodies against type I interferons as an additional diagnostic criterion for autoimmune polyendocrine syndrome type I.
Meloni A; Furcas M; Cetani F; Marcocci C; Falorni A; Perniola R; Pura M; Bøe Wolff AS; Husebye ES; Lilic D; Ryan KR; Gennery AR; Cant AJ; Abinun M; Spickett GP; Arkwright PD; Denning D; Costigan C; Dominguez M; McConnell V; Willcox N; Meager A
J Clin Endocrinol Metab; 2008 Nov; 93(11):4389-97. PubMed ID: 18728167
[TBL] [Abstract][Full Text] [Related]
10. Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients.
Garelli S; Dalla Costa M; Sabbadin C; Barollo S; Rubin B; Scarpa R; Masiero S; Fierabracci A; Bizzarri C; Crinò A; Cappa M; Valenzise M; Meloni A; De Bellis AM; Giordano C; Presotto F; Perniola R; Capalbo D; Salerno MC; Stigliano A; Radetti G; Camozzi V; Greggio NA; Bogazzi F; Chiodini I; Pagotto U; Black SK; Chen S; Rees Smith B; Furmaniak J; Weber G; Pigliaru F; De Sanctis L; Scaroni C; Betterle C
J Endocrinol Invest; 2021 Nov; 44(11):2493-2510. PubMed ID: 34003463
[TBL] [Abstract][Full Text] [Related]
11. The heterogeneity of autoimmune polyendocrine syndrome type 1: Clinical features, new mutations and cytokine autoantibodies in a Brazilian cohort from tertiary care centers.
Weiler FG; Peterson P; Costa-Carvalho BT; de Barros Dorna M; Correia-Deur JE; Sader SL; Espíndola-Antunes D; Guerra-Junior G; Dias-da-Silva MR; Lazaretti-Castro M
Clin Immunol; 2018 Dec; 197():231-238. PubMed ID: 30287219
[TBL] [Abstract][Full Text] [Related]
12. Novel sequence variation of AIRE and detection of interferon-omega antibodies in early infancy.
Tóth B; Wolff AS; Halász Z; Tar A; Szüts P; Ilyés I; Erdos M; Szegedi G; Husebye ES; Zeher M; Maródi L
Clin Endocrinol (Oxf); 2010 May; 72(5):641-7. PubMed ID: 19863576
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. An 8-year-old boy with autoimmune hepatitis and Candida onychosis as the first symptoms of autoimmune polyglandular syndrome (APS1): identification of a new homozygous mutation in the autoimmune regulator gene (AIRE).
Lintas C; Cappa M; Comparcola D; Nobili V; Fierabracci A
Eur J Pediatr; 2008 Aug; 167(8):949-53. PubMed ID: 17891543
[TBL] [Abstract][Full Text] [Related]
15. Autoimmune polyendocrine syndrome type I in Slovakia: relevance of screening patients with autoimmune Addison's disease.
F Magitta N; Pura M; S Bøe Wolff A; Vanuga P; Meager A; M Knappskog P; Husebye ES
Eur J Endocrinol; 2008 May; 158(5):705-9. PubMed ID: 18426830
[TBL] [Abstract][Full Text] [Related]
16. Genetic dissection of autoimmune polyendocrine syndrome type 2: common origin of a spectrum of phenotypes.
Ballarini A; Lee-Kirsch MA
Ann N Y Acad Sci; 2007 Sep; 1110():159-65. PubMed ID: 17911431
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Identification of autoimmune polyendocrine syndrome type 1 in patients with isolated hypoparathyroidism.
Sahoo SK; Zaidi G; Srivastava R; Sarangi AN; Bharti N; Eriksson D; Bensing S; Kämpe O; Aggarwal A; Aggarwal R; Bhatia E
Clin Endocrinol (Oxf); 2016 Oct; 85(4):544-50. PubMed ID: 27219120
[TBL] [Abstract][Full Text] [Related]
19. A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients.
Rosatelli MC; Meloni A; Meloni A; Devoto M; Cao A; Scott HS; Peterson P; Heino M; Krohn KJ; Nagamine K; Kudoh J; Shimizu N; Antonarakis SE
Hum Genet; 1998 Oct; 103(4):428-34. PubMed ID: 9856486
[TBL] [Abstract][Full Text] [Related]
20. Addison's disease: a survey on 633 patients in Padova.
Betterle C; Scarpa R; Garelli S; Morlin L; Lazzarotto F; Presotto F; Coco G; Masiero S; Parolo A; Albergoni MP; Favero R; Barollo S; Salvà M; Basso D; Chen S; Rees Smith B; Furmaniak J; Mantero F
Eur J Endocrinol; 2013 Dec; 169(6):773-84. PubMed ID: 24014553
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
