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1. Homozygous haemoglobin O disease and conjugated hyperbilirubinaemia in a Sudanese family.

Authors: S A Ibrahim; D Mustafa; A O Mohamed; M B Mohed
Journal: BMJ Date: 1992-01-04

Review 2. Hepatic transport and metabolism of various organic anions in patients with congenital non-hemolytic hyperbilirubinemia, including constitutional indocyanine green excretory defect.

Authors: M Nambu; T Namihisa
Journal: J Gastroenterol Date: 1994-04 Impact factor: 7.527

3. Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2.

Authors: Lenka Slachtova; Ondrej Seda; Jana Behunova; Martin Mistrik; Pavel Martasek
Journal: Eur J Hum Genet Date: 2015-09-09 Impact factor: 4.246

Review 4. Gene replacement therapy for genetic hepatocellular jaundice.

Authors: Remco van Dijk; Ulrich Beuers; Piter J Bosma
Journal: Clin Rev Allergy Immunol Date: 2015-06 Impact factor: 8.667

5. Dubin-Johnson syndrome in a neonate.

Authors: F Nakata; K Oyanagi; M Fujiwara; H Sogawa; R Minami; K Horino; T Nakao; T Kondo
Journal: Eur J Pediatr Date: 1979 Impact factor: 3.183

6. Coproporphyrin I and 3 excretion in bile and urine.

Authors: N Kaplowitz; N Javitt; A Kappas
Journal: J Clin Invest Date: 1972-11 Impact factor: 14.808

7. Endogenous Coproporphyrin I and III are Altered in Multidrug Resistance-Associated Protein 2-Deficient (TR^-) Rats.

Authors: Jacqueline Bezençon; Chitra Saran; Janine Hussner; James J Beaudoin; Yueping Zhang; Hong Shen; John K Fallon; Philip C Smith; Henriette E Meyer Zu Schwabedissen; Kim L R Brouwer
Journal: J Pharm Sci Date: 2020-10-13 Impact factor: 3.534