Gilbert's syndrome: evidence of morphological heterogeneity.

Author:

Dawson J,Carr-Locke D L,Talbot I C,Rosenthal F D

Publisher

BMJ

Subject

Gastroenterology

Reference30 articles.

1. Chronic unconjugated hyperbilirubinemia without overt signs of hemolysis in adolescents and adults;Arias, I.M.;Journal of Clinical Investigation,1962

2. Bilirubin and paranitrophenol glucuronyl transferase activities of the liver in patients with Gilbert's syndrome. An attempt at a biochemical breakdown of the Gilbert's syndrome;Auclair, C.; Hakim, J.; Boivin, P.; Troube, H.; Boucherot, J.;Enzyme,1976

3. Hyperbilirubinemia of fasting;Barrett, P.V.D.;Journal of the American Medical Association,1971

4. Excess lipofuscin accumulation in constitutional hepatic dysfunction (Gilbert's syndrome) light and electron microscopic observations;Barth, R.F.; Grimley, P.M.; Berk, P.D.; Bloomer, J.R.; Howe, R.B.;Archives of Pathology,1971

5. Constitutional hepatic dysfunction (Gilbert's syndrome). A new definition based on kinetic studies with unconjugated radiobilirubin;Berk, P.D.; Bloomer, J.R.; Howe, R.B.; Berlin, N.I.;American Journal of Medicine,1970

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