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4. 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; 475(3):373-381. PubMed ID: 30911814 [TBL] [Abstract][Full Text] [Related]
5. Rituximab was used to treat recurrent IgG4-related hypophysitis with ophthalmopathy as the initial presentation: A case report and literature review. Gu WJ; Zhang Q; Zhu J; Li J; Wei SH; Mu YM Medicine (Baltimore); 2017 Jun; 96(24):e6934. PubMed ID: 28614220 [TBL] [Abstract][Full Text] [Related]
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11. 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; 18(5):722-30. PubMed ID: 25822111 [TBL] [Abstract][Full Text] [Related]
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14. 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; 56(9):1033-41. PubMed ID: 19926920 [TBL] [Abstract][Full Text] [Related]
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16. 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; 57(6):485-92. PubMed ID: 20371985 [TBL] [Abstract][Full Text] [Related]
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20. Clinical course of IgG4-related hypophysitis presenting with focal seizure and relapsing lymphocytic hypophysitis. Ngaosuwan K; Trongwongsa T; Shuangshoti S BMC Endocr Disord; 2015 Oct; 15():64. PubMed ID: 26510826 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]