Familial and nonfamilial benign recurrent cholestiasis distinguished by plasma disappearance of indocyanine green but not cholylglycine.

Author:

van Berge-Henegouwen G P,Ferguson D R,Hofmann A F,De Pagter A G

Publisher

BMJ

Subject

Gastroenterology

Reference24 articles.

1. Plasma elimination of a tracer dose of cholyl (1-14C) glycine in liver disease;Barnes, S.; Thjodleifsson, B.; Billing, B.H.; Sherlock, S.;Clinical Science and Molecular Medicine,1976

2. Is an acute disturbance in hepatic transport of bile acids the primary cause of cholestasis in benign recurrent cholestasis?;van Berge-Henegouwen, G.P.; Brandt, K.-H.; de Pagter, A.G.F.;Lancet,1974

3. Studies of intestinal digestion and absorption in the human;Borgstrom, B.; Dahlqvist, A.; Lundh, G.; Sj6vall, J.;Journal of Clinical Investigation,1957

4. Development of a simple, safe, bile acid clearance test: The radio-cholate clearance test;Calcraft, B.; LaRusso, N.F.; Hofmann, A.F.; Belobaba, D.T.A.;Gastroenterology,1975

5. Serum bile acid concentrations in patients with liver disease;Fausa, O.; Gjone, E.;Scandinavian Journal of Gastroenterology,1976

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