1. Studies of chronic familial non-hemolytic jaundice with conjugated bilirubin in the serum with and without an unidentified pigment in the liver cells;Arias, I.M.;American Journal of Medicine,1961
2. Inheritable and congenital hyperbilirubinemia. Models for the study of drug metabolism;Arias, I.M.;New England Journal of Medicine,1971
3. Familial Dubin-Johnson syndrome;Beker, S.; Read, A.E.;Gastroenterology,1958
4. 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 ofMedicine,1970
5. Studies of chronic idiopathic jaundice (Dubin-Johnson syndrome). II. Evaluation of a large family with the trait;Butt, H.R.; Anderson, V.E.; Foulk, W.T.; Baggenstoss, A.H.; Schoenfield, L.J.; Dickson, E.R.;Gastroenterology,1966