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Journal Abstract Search

255 related items for PubMed ID: 16792967

  • 1. [AIRE gene mutation in polyglandular syndrome type 1].
    Martínez López MM, González Casado I, Alvarez Doforno R, Delgado Cerviño E, Gracia Bouthelier R.
    An Pediatr (Barc); 2006 Jun; 64(6):583-7. PubMed ID: 16792967
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  • 2. Polyglandular autoimmune syndrome type I - a novel AIRE mutation in a North American patient.
    Huibregtse KE, Wolfgram P, Winer KK, Connor EL.
    J Pediatr Endocrinol Metab; 2014 Nov; 27(11-12):1257-60. PubMed ID: 24945421
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  • 3. Precocious presentation of autoimmune polyglandular syndrome type 2 associated with an AIRE mutation.
    Resende E, Gόmez GN, Nascimento M, Loidi L, Saborido Fiaño R, Cabanas Rodrίguez P, Castro-Feijoo L, Barreiro Conde J.
    Hormones (Athens); 2015 Nov; 14(2):312-6. PubMed ID: 25402387
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  • 5. Autoimmune polyglandular syndrome type 1 in Russian patients: clinical variants and autoimmune regulator mutations.
    Orlova EM, Bukina AM, Kuznetsova ES, Kareva MA, Zakharova EU, Peterkova VA, Dedov II.
    Horm Res Paediatr; 2010 Nov; 73(6):449-57. PubMed ID: 20407228
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  • 6. 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
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  • 8. Autoimmune regulator AIRE: evidence for genetic differences between autoimmune hepatitis and hepatitis as part of the autoimmune polyglandular syndrome type 1.
    Vogel A, Liermann H, Harms A, Strassburg CP, Manns MP, Obermayer-Straub P.
    Hepatology; 2001 May; 33(5):1047-52. PubMed ID: 11343230
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  • 11. Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl.
    Kollios K, Tsolaki A, Antachopoulos C, Moix I, Morris MA, Papadopoulou M, Roilides E.
    J Pediatr Endocrinol Metab; 2011 May; 24(7-8):599-601. PubMed ID: 21932610
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  • 15. [Autoimmune polyglandular syndromes].
    Lankisch TO, Jaeckel E, Strassburg CP, Manns MP.
    Internist (Berl); 2005 Jul; 46(7):750-8. PubMed ID: 15947901
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  • 16. Rapid whole-genome sequencing identifies a novel AIRE variant associated with autoimmune polyendocrine syndrome type 1.
    Sanford E, Watkins K, Nahas S, Gottschalk M, Coufal NG, Farnaes L, Dimmock D, Kingsmore SF, RCIGM Investigators.
    Cold Spring Harb Mol Case Stud; 2018 Jun; 4(3):. PubMed ID: 29437776
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  • 20. Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy: report of three cases from Iran.
    Seifi-Alan M, Shamsi R, Setoodeh A, Sayarifard F, Aghasi P, Kompani F, Ghafouri-Fard S, Abbasi F.
    J Pediatr Endocrinol Metab; 2016 Aug 01; 29(8):979-83. PubMed ID: 27105486
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