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OBJECTIVES: Type I autoimmune pancreatitis (AIP) and IgG4-related sclerosing cholangitis (IgG4-related SC) are now recognized as components of a multisystem IgG4-related disease (IgG4-RD). We aimed to define the clinical course and long-term outcomes in patients with AIP/IgG4-SC recruited from two large UK tertiary referral centers.

Original publication

DOI

10.1038/ajg.2014.223

Type

Journal article

Journal

The American journal of gastroenterology

Publication Date

01/10/2014

Volume

109

Pages

1675 - 1683