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Morphologic Findings in Progressive Familial Intrahepatic Cholestasis 2 (PFIC2): Correlation With Genetic and Immunohistochemical Studies

K Evason, KE Bove, MJ Finegold… - … American journal of …, 2011 - journals.lww.com
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Bile Acid Signaling in Fetal Tissues: Implications for Intrahepatic Cholestasis of Pregnancy

C Williamson, M Miragoli… - Digestive …, 2011 - content.karger.com
Background/Aims: Intrahepatic cholestasis of pregnancy (ICP) is complicated by spontaneous
preterm labor, fetal anoxia and unexplained fetal death. We aim to evaluate the mechanisms
by which raised fetal bile acids cause placental abnormalities and fetal cardiac pathology. ...
Related articles - All 2 versions

Progressive Familial Intrahepatic Cholestasis (PFIC) Type 1, 2, and 3: A Review of the Liver Pathology Findings

RA Morotti, FJ Suchy… - Seminars in liver disease, 2011 - thieme-connect.com
Progressive familial intrahepatic cholestatic diseases encompass a group of autosomal recessive
hereditary diseases, which usually present in infancy or childhood, with cholestasis of hepatocellular
origin. The currently preferred nomenclature for the three PFIC disorders that have been ...
Cited by 1 - Related articles - All 3 versions

Primary Dermatologic Findings With Early-Onset Intrahepatic Cholestasis of Pregnancy

TT Chao… - Obstetrics & Gynecology, 2011 - journals.lww.com
Wolters Kluwer Health may email you for journal alerts and information, but is committed to maintaining
your privacy and will not share your personal information without your express consent. For more
information, please refer to our Privacy Policy. ... Skip Navigation Links Home > February ...
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A new Caucasian case of neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD): A clinical, molecular, and functional study

G Fiermonte, G Parisi, D Martinelli… - Molecular Genetics and …, 2011 - Elsevier
Citrin is the liver-specific isoform of the mitochondrial aspartate/glutamate carrier (AGC2). AGC2
deficiency is an autosomal recessive disorder with two age related phenotypes: neonatal intrahepatic
cholestasis (NICCD, OMIM#605814) and adult-onset type II citrullinemia (CTLN2, OMIM# ...

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