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- W4237935781 endingPage "1301" @default.
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- W4237935781 abstract "Over the course of the last 2 decades our knowledge of autoimmune pancreatitis has increased exponentially. In this review, we summarize the clinical presentation, diagnosis and treatment of AIP, to better allow general gastroenterologists and primary care providers to consider AIP as a as a rare but important cause of painless obstructive jaundice and recurrent acute pancreatitis. While steroids remain the mainstay of first line therapy, a number of patients with type 1 AIP require immunomodulators or rituximab to maintain remission; recommendations on the management of relapses continue to evolve." @default.
- W4237935781 created "2022-05-12" @default.
- W4237935781 creator A5001178798 @default.
- W4237935781 creator A5007797661 @default.
- W4237935781 creator A5048460582 @default.
- W4237935781 date "2018-09-01" @default.
- W4237935781 modified "2023-10-14" @default.
- W4237935781 title "Autoimmune Pancreatitis" @default.
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- W4237935781 doi "https://doi.org/10.1038/s41395-018-0146-0" @default.
- W4237935781 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29910463" @default.
- W4237935781 hasPublicationYear "2018" @default.
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