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©The Author(s) 2017.
World J Gastroenterol. Oct 21, 2017; 23(39): 7191-7197
Published online Oct 21, 2017. doi: 10.3748/wjg.v23.i39.7191
Published online Oct 21, 2017. doi: 10.3748/wjg.v23.i39.7191
Figure 3 Biochemical responses to ursodeoxycholic acid treatment.
A-D: Serum activities of aspartate aminotransferase (AST; solid lines) and alkaline phosphatase (ALP; dotted lines) showing good responses to ursodeoxycholic acid in patients 1-4.
- Citation: Shin S, Moh IH, Woo YS, Jung SW, Kim JB, Park JW, Suk KT, Kim HS, Hong M, Park SH, Lee MS. Evidence from a familial case suggests maternal inheritance of primary biliary cholangitis. World J Gastroenterol 2017; 23(39): 7191-7197
- URL: https://www.wjgnet.com/1007-9327/full/v23/i39/7191.htm
- DOI: https://dx.doi.org/10.3748/wjg.v23.i39.7191