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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1954 1
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1958 10
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1961 11
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1963 30
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1966 27
1967 26
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1970 33
1971 34
1972 27
1973 26
1974 16
1975 27
1976 21
1977 18
1978 14
1979 17
1980 17
1981 5
1982 14
1983 10
1984 7
1985 7
1986 3
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1988 12
1989 1
1990 10
1991 9
1992 12
1993 12
1994 9
1995 4
1996 10
1997 12
1998 17
1999 14
2000 20
2001 13
2002 14
2003 13
2004 12
2005 15
2006 16
2007 12
2008 5
2009 9
2010 12
2011 9
2012 9
2013 10
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2015 11
2016 9
2017 12
2018 9
2019 12
2020 8
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992 results

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Page 1
Dubin-Johnson Syndrome.
Noe Del Cueto-Aguilera A, García-Compean D, Scharrer Cabello SI, González-González JA. Noe Del Cueto-Aguilera A, et al. Am J Gastroenterol. 2020 Sep;115(9):1386. doi: 10.14309/ajg.0000000000000519. Am J Gastroenterol. 2020. PMID: 32886872 No abstract available.
Dubin-Johnson syndrome.
Powell KC, Anderson RH, Shepherd AR, Wilkey IS, Cooke RA. Powell KC, et al. Med J Aust. 1970 May 9;1(19):957-8. doi: 10.5694/j.1326-5377.1970.tb116714.x. Med J Aust. 1970. PMID: 5422568 No abstract available.
[Dubin-Johnson syndrome].
Itoh S. Itoh S. Ryoikibetsu Shokogun Shirizu. 2001;(33):569-70. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462574 Review. Japanese. No abstract available.
Dubin-Johnson syndrome.
Nisa AU, Ahmad Z. Nisa AU, et al. J Coll Physicians Surg Pak. 2008 Mar;18(3):188-9. J Coll Physicians Surg Pak. 2008. PMID: 18460254
Clinical suspicion of Dubin-Johnson syndrome was raised. Liver biopsy showed diffuse deposition of coarse granular dark brown pigment in hepatocytes. Dubin-Johnson syndrome is a benign condition, which results from a hereditary defect in …
Clinical suspicion of Dubin-Johnson syndrome was raised. Liver biopsy showed diffuse deposition of coarse granular dark …
[Dubin-Johnson syndrome].
Tazuma S, Miura H, Nakanishi T, Kajiyama G. Tazuma S, et al. Ryoikibetsu Shokogun Shirizu. 1995;(8):424-6. Ryoikibetsu Shokogun Shirizu. 1995. PMID: 8581669 Review. Japanese. No abstract available.
[Dubin-Johnson syndrome].
Itoh S, Onishi S. Itoh S, et al. Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):267-70. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9645057 Review. Japanese. No abstract available.
[The Dubin-Johnson syndrome].
Schillinger H. Schillinger H. Med Klin. 1967 Feb 3;62(5):161-6. Med Klin. 1967. PMID: 4874101 Review. German. No abstract available.
Neonatal Dubin-Johnson syndrome: biochemical parameters, characteristics, and genetic variants study.
Fu H, Zhao R, Jia X, Li X, Li G, Yin C. Fu H, et al. Pediatr Res. 2022 May;91(6):1571-1578. doi: 10.1038/s41390-021-01583-7. Epub 2021 May 28. Pediatr Res. 2022. PMID: 34050268
BACKGROUND: The clinical characteristics and gene mutation characteristics of children with Dubin-Johnson syndrome (DJS) need in-depth study. METHODS: The clinical and genomic data of neonatal Dubin-Johnson syndrome (NDJS) and 155 cases w …
BACKGROUND: The clinical characteristics and gene mutation characteristics of children with Dubin-Johnson syndrome (DJS …
Dubin-Johnson Syndrome as Differential Diagnosis for Neonatal Cholestasis.
Junge N, Goldschmidt I, Wiegandt J, Leiskau C, Mutschler F, Laue T, Ohlendorf J, Stalke A, Hartleben B, Stindt J, Keitel V, Baumann U, Pfister ED. Junge N, et al. J Pediatr Gastroenterol Nutr. 2021 May 1;72(5):e105-e111. doi: 10.1097/MPG.0000000000003061. J Pediatr Gastroenterol Nutr. 2021. PMID: 33534365
OBJECTIVES: Dubin-Johnson syndrome (DJS) is an autosomal recessive disorder in which multidrug-resistance-associated protein 2 (MRP2) deficiency causes an excretion disorder of conjugated bilirubin from hepatocytes into bile canaliculi. ...
OBJECTIVES: Dubin-Johnson syndrome (DJS) is an autosomal recessive disorder in which multidrug-resistance-associated pr …
Dubin-Johnson syndrome as a laparoscopic finding.
Cebrián García A, Ruiz-Clavijo García D, Larrea Ramírez A, Arín Palacios B. Cebrián García A, et al. Rev Esp Enferm Dig. 2021 Aug;113(8):610-611. doi: 10.17235/reed.2021.7866/2021. Rev Esp Enferm Dig. 2021. PMID: 33657825 Free article.
We present the case of a 35-year-old female with a history of polycystic ovary syndrome, treated with oral contraceptives. She was under study due to nine months evolution of pain in the right iliac fossa, associated with hyporexia and mild hyperbilirubinemia with a predom …
We present the case of a 35-year-old female with a history of polycystic ovary syndrome, treated with oral contraceptives. She was un …
992 results