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PUBMED FOR HANDHELDS

Journal Abstract Search


317 related items for PubMed ID: 23515454

  • 1. A case of IgG4-related hypophysitis without pituitary insufficiency.
    Hattori Y, Tahara S, Ishii Y, Kitamura T, Inomoto C, Osamura RY, Teramoto A, Morita A.
    J Clin Endocrinol Metab; 2013 May; 98(5):1808-11. PubMed ID: 23515454
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  • 2. Prednisolone-responsive Postpartum IgG4-related Hypophysitis.
    Koide H, Shiga A, Komai E, Yamato A, Fujimoto M, Tamura A, Kono T, Nakayama A, Takiguchi T, Higuchi S, Sakuma I, Nagano H, Hashimoto N, Suzuki S, Takeda Y, Shibuya M, Nishioka H, Yamada S, Inoshita N, Ishiwatari N, Horiguchi K, Yokote K, Tanaka T.
    Intern Med; 2018 Feb 01; 57(3):367-375. PubMed ID: 29093382
    [Abstract] [Full Text] [Related]

  • 3. Hypophysitis presenting with atypical rapid deterioration: with special reference to immunoglobulin G4-related disease-case report-.
    Osawa S, Ogawa Y, Watanabe M, Tominaga T.
    Neurol Med Chir (Tokyo); 2009 Dec 01; 49(12):622-5. PubMed ID: 20035143
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  • 5. Anti-pituitary antibodies against corticotrophs in IgG4-related hypophysitis.
    Iwata N, Iwama S, Sugimura Y, Yasuda Y, Nakashima K, Takeuchi S, Hagiwara D, Ito Y, Suga H, Goto M, Banno R, Caturegli P, Koike T, Oshida Y, Arima H.
    Pituitary; 2017 Jun 01; 20(3):301-310. PubMed ID: 27896569
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  • 6. IgG4-related hypophysitis in adolescence.
    Arya VB, El-Gasim SA, Das S, Reisz Z, Zebian B, D'Cruz D, King A, Hampton T, Aylwin SJB, Kapoor RR, Buchanan CR.
    J Pediatr Endocrinol Metab; 2021 Mar 26; 34(3):395-399. PubMed ID: 33675204
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  • 7. Prednisolone markedly reduced serum IgG4 levels along with the improvement of pituitary mass and anterior pituitary function in a patient with IgG4-related infundibulo-hypophysitis.
    Iseda I, Hida K, Tone A, Tenta M, Shibata Y, Matsuo K, Yamadori I, Hashimoto K.
    Endocr J; 2014 Mar 26; 61(2):195-203. PubMed ID: 24335007
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  • 8. Hypophysitis due to IgG4-related disease responding to treatment with azathioprine: an alternative to corticosteroid therapy.
    Caputo C, Bazargan A, McKelvie PA, Sutherland T, Su CS, Inder WJ.
    Pituitary; 2014 Jun 26; 17(3):251-6. PubMed ID: 23794123
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  • 9. Concurrent IgG4-related hypophysitis and clinically nonfunctioning gonadotroph pituitary neuroendocrine tumor.
    Tahara S, Osamura RY, Hattori Y, Ishisaka E, Inomoto C, Sugihara H, Teramoto A, Morita A.
    BMC Endocr Disord; 2023 May 04; 23(1):96. PubMed ID: 37143052
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  • 10. Mikulicz's Disease with hypophysitis - a new IgG4-mediated disorder.
    Bhagwat NM, Tayde PS, Dalwadi PP, Sorabjee J, Varthakavi PK.
    Endokrynol Pol; 2016 May 04; 67(6):622-626. PubMed ID: 28042654
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  • 11. IgG4-related hypophysitis: a new addition to the hypophysitis spectrum.
    Leporati P, Landek-Salgado MA, Lupi I, Chiovato L, Caturegli P.
    J Clin Endocrinol Metab; 2011 Jul 04; 96(7):1971-80. PubMed ID: 21593109
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  • 12. The prevalence of IgG4-positive plasma cells in hypophysitis: a possible relationship to IgG4-related disease.
    Tauziede-Espariat A, Polivka M, Bouazza S, Decq P, Robert G, Laloi-Michelin M, Adle-Biassette H.
    Clin Neuropathol; 2015 Jul 04; 34(4):181-92. PubMed ID: 25828777
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  • 13. Disease heterogeneity in IgG4-related hypophysitis: report of two histopathologically proven cases and review of the literature.
    Uccella S, Amaglio C, Brouland JP, Bianconi E, Ippolito S, Messerer M, Rouiller N, Tanda ML, Sessa F, La Rosa S.
    Virchows Arch; 2019 Sep 04; 475(3):373-381. PubMed ID: 30911814
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  • 15. Long-term clinical course of IgG4-related systemic disease accompanied by hypophysitis.
    Hori M, Makita N, Andoh T, Takiyama H, Yajima Y, Sakatani T, Fukumoto S, Iiri T, Fujita T.
    Endocr J; 2010 Sep 04; 57(6):485-92. PubMed ID: 20371985
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  • 16. IgG4-related Hypophysitis with Subtle Hypopituitarism in an Elderly Diabetic Patient: Is Treatment or Observation Preferable?
    Kawasaki M, Tsujino M, Sato F, Sakurada M, Nishida K, Kise T, Hijioka Y, Ishizawa M, Enatsu K, Ogawa Y.
    Intern Med; 2017 Oct 15; 56(20):2733-2738. PubMed ID: 28924128
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  • 17. Pituitary and stalk lesions (infundibulo-hypophysitis) associated with immunoglobulin G4-related systemic disease: an emerging clinical entity.
    Shimatsu A, Oki Y, Fujisawa I, Sano T.
    Endocr J; 2009 Oct 15; 56(9):1033-41. PubMed ID: 19926920
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  • 18. Central Diabetes Insipidus Due to IgG4-related Hypophysitis That Required over One Year to Reach the Final Diagnosis Due to Symptoms Being Masked by Sialadenitis.
    Iwamoto Y, Mori S, Tatsumi F, Sugisaki T, Dan K, Katakura Y, Kimura T, Shimoda M, Nakanishi S, Mune T, Kaneto H.
    Intern Med; 2022 Dec 01; 61(23):3541-3545. PubMed ID: 35569983
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  • 19. Bilateral dacryoadenitis complicated by lymphocytic hypophysitis.
    Baoke H, Shihui W, Maonian Z, Zhaohui L, Zhitong Z, Zhigang S, Yan H.
    J Neuroophthalmol; 2009 Sep 01; 29(3):214-8. PubMed ID: 19726944
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  • 20. A diagnostic pitfall in IgG4-related hypophysitis: infiltration of IgG4-positive cells in the pituitary of granulomatosis with polyangiitis.
    Bando H, Iguchi G, Fukuoka H, Taniguchi M, Kawano S, Saitoh M, Yoshida K, Matsumoto R, Suda K, Nishizawa H, Takahashi M, Morinobu A, Kohmura E, Ogawa W, Takahashi Y.
    Pituitary; 2015 Oct 01; 18(5):722-30. PubMed ID: 25822111
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