K Evason, KE Bove, MJ Finegold… - … American journal of …, 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 > Current ... Cited by 2 - Related articles - All 3 versions
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
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
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 ... Related articles - All 3 versions
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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