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Quoted phrase not found in phrase index: "Hypercholanemia, familial 1"
Page 1
Recognition of asymptomatic hypercholanemia of pregnancy: Different clinical features, fetal outcomes and bile acids metabolism from intrahepatic cholestasis of pregnancy.
He Y, Zhang X, Shao Y, Xu B, Cui Y, Chen X, Chen H, Luo C, Ding M. He Y, et al. Biochim Biophys Acta Mol Basis Dis. 2022 Jan 1;1868(1):166269. doi: 10.1016/j.bbadis.2021.166269. Epub 2021 Sep 17. Biochim Biophys Acta Mol Basis Dis. 2022. PMID: 34537368 Free article.

RESULTS: The risk of adverse fetal outcomes in AHP (28.3%) was significantly higher than that in normal pregnancies (8.9%, p < 0.001), but lower than that in ICP group (52.1%, p < 0.001). Multivariate statistics analysis indicated a distinctive serum BAs metabolic pr

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RESULTS: The risk of adverse fetal outcomes in AHP (28.3%) was significantly higher than that in normal pregnancies (8.9%, p < 0.001), bu

…
ATP8B1 and ATP11C: Two Lipid Flippases Important for Hepatocyte Function.
Naik J, de Waart DR, Utsunomiya K, Duijst S, Mok KH, Oude Elferink RP, Bosma PJ, Paulusma CC. Naik J, et al. Dig Dis. 2015;33(3):314-8. doi: 10.1159/000371665. Epub 2015 May 27. Dig Dis. 2015. PMID: 26045263
Mutation of ATP8B1 cause progressive familial Intrahepatic Cholestasis type 1 (PFIC1)and benign recurrent intrahepatic cholestasis type 1 (BRIC 1). ...
Mutation of ATP8B1 cause progressive familial Intrahepatic Cholestasis type 1 (PFIC1)and benign recurrent intrahepatic cholestasis ty …