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Journal Abstract Search

395 related items for PubMed ID: 25402387

  • 1. 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; 14(2):312-6. PubMed ID: 25402387
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. [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
    [Abstract] [Full Text] [Related]

  • 4. Distinct clinical phenotype and immunoreactivity in Japanese siblings with autoimmune polyglandular syndrome type 1 (APS-1) associated with compound heterozygous novel AIRE gene mutations.
    Kogawa K, Kudoh J, Nagafuchi S, Ohga S, Katsuta H, Ishibashi H, Harada M, Hara T, Shimizu N.
    Clin Immunol; 2002 Jun; 103(3 Pt 1):277-83. PubMed ID: 12173302
    [Abstract] [Full Text] [Related]

  • 5. A Case of Autoimmune Poly Glandular Glandular Syndrome Type 2 (Schmidt's Syndrome).
    V BV.
    J Assoc Physicians India; 2023 Jan; 71(1):1. PubMed ID: 37116019
    [Abstract] [Full Text] [Related]

  • 6. A new mutation site in the AIRE gene causes autoimmune polyendocrine syndrome type 1.
    Zhu W, Hu Z, Liao X, Chen X, Huang W, Zhong Y, Zeng Z.
    Immunogenetics; 2017 Oct; 69(10):643-651. PubMed ID: 28540407
    [Abstract] [Full Text] [Related]

  • 7. HLA class II haplotypes differentiate between the adult autoimmune polyglandular syndrome types II and III.
    Flesch BK, Matheis N, Alt T, Weinstock C, Bux J, Kahaly GJ.
    J Clin Endocrinol Metab; 2014 Jan; 99(1):E177-82. PubMed ID: 24187405
    [Abstract] [Full Text] [Related]

  • 8. Autoimmune adrenal insufficiency in children: a hint for polyglandular syndrome type 2?
    Arrigoni M, Cavarzere P, Nicolussi Principe L, Gaudino R, Antoniazzi F.
    Ital J Pediatr; 2023 Jul 29; 49(1):94. PubMed ID: 37516895
    [Abstract] [Full Text] [Related]

  • 9. Report of two siblings with APECED in Serbia: is there a founder effect of c.769C>T AIRE genotype?
    Fierabracci A, Lanzillotta M, Vorgučin I, Palma A, Katanić D, Betterle C.
    Ital J Pediatr; 2021 Jun 02; 47(1):126. PubMed ID: 34078422
    [Abstract] [Full Text] [Related]

  • 10. 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 02; 102(3):163-8. PubMed ID: 23643663
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  • 12. 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 Sep 02; 73(6):449-57. PubMed ID: 20407228
    [Abstract] [Full Text] [Related]

  • 13. Autoimmune polyglandular syndrome type 1 with diabetes insipidus: a case report.
    Chen J, Lu T, Liu C, Zhao Y, Huang A, Hu X, Li M, Xiang R, Feng M, Lu H.
    BMC Endocr Disord; 2021 Aug 03; 21(1):154. PubMed ID: 34344344
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  • 17. 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 03; 27(11-12):1257-60. PubMed ID: 24945421
    [Abstract] [Full Text] [Related]

  • 18. 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 03; 92(2):595-603. PubMed ID: 17118990
    [Abstract] [Full Text] [Related]

  • 19. 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 Feb 03; 24(7-8):599-601. PubMed ID: 21932610
    [Abstract] [Full Text] [Related]

  • 20. Type 1 Diabetes in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Syndrome (APECED): A "Rare" Manifestation in a "Rare" Disease.
    Fierabracci A.
    Int J Mol Sci; 2016 Jul 12; 17(7):. PubMed ID: 27420045
    [Abstract] [Full Text] [Related]

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