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Items: 1 to 20 of 115

1.

Hyperbilirubinemia syndromes (Gilbert-Meulengracht, Crigler-Najjar, Dubin-Johnson, and Rotor syndrome).

Strassburg CP.

Best Pract Res Clin Gastroenterol. 2010 Oct;24(5):555-71. doi: 10.1016/j.bpg.2010.07.007. Review.

PMID:
20955959
2.

Inherited disorders of bilirubin clearance.

Memon N, Weinberger BI, Hegyi T, Aleksunes LM.

Pediatr Res. 2016 Mar;79(3):378-86. doi: 10.1038/pr.2015.247. Epub 2015 Nov 23. Review.

3.

Hereditary hyperbilirubinemias.

Radlović N.

Srp Arh Celok Lek. 2014 Mar-Apr;142(3-4):257-60. Review.

4.

Nonhemolytic hyperbilirubinemias.

Hollander IJ.

Ann Clin Lab Sci. 1980 May-Jun;10(3):204-8. Review.

PMID:
6994579
5.

Congenital nonhemolytic hyperbilirubinemias.

Cichoz-Lach H, Celiński K, Słomka M.

Ann Univ Mariae Curie Sklodowska Med. 2004;59(1):449-52.

PMID:
16146029
6.

[Inherited disorders of bilirubin metabolism].

Rossi F, Francese M, Iodice RM, Falcone E, Vetrella S, Punzo F, De Vita S, Perrotta S.

Minerva Pediatr. 2005 Apr;57(2):53-63. Review. Italian.

PMID:
15985997
7.

Inherited disorders of bilirubin transport and conjugation: new insights into molecular mechanisms and consequences.

Erlinger S, Arias IM, Dhumeaux D.

Gastroenterology. 2014 Jun;146(7):1625-38. doi: 10.1053/j.gastro.2014.03.047. Epub 2014 Apr 1. Review.

PMID:
24704527
8.

[Gilbert disease and type I and II Crigler-Najjar syndrome due to mutations in the same UGT1A1 gene locus].

Kraemer D, Scheurlen M.

Med Klin (Munich). 2002 Sep 15;97(9):528-32. Review. German.

PMID:
12371080
9.

Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype.

Kadakol A, Ghosh SS, Sappal BS, Sharma G, Chowdhury JR, Chowdhury NR.

Hum Mutat. 2000 Oct;16(4):297-306. Review.

PMID:
11013440
10.

Gene replacement therapy for genetic hepatocellular jaundice.

van Dijk R, Beuers U, Bosma PJ.

Clin Rev Allergy Immunol. 2015 Jun;48(2-3):243-53. doi: 10.1007/s12016-014-8454-7. Review.

PMID:
25315738
11.

Genes for jaundice.

Hardikar W.

J Paediatr Child Health. 1999 Dec;35(6):522-4. Review.

PMID:
10620165
12.

Familial unconjugated hyperbilirubinemia syndromes.

Reichen J.

Semin Liver Dis. 1983 Feb;3(1):24-35.

PMID:
6836332
14.

[Congenital nonhemolytic hyperbilirubinemias].

Wehinger H.

Med Klin. 1977 Sep 16;72(37):1463-72. Review. German. No abstract available.

PMID:
409916
15.

Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome.

Maruo Y, Nakahara S, Yanagi T, Nomura A, Mimura Y, Matsui K, Sato H, Takeuchi Y.

J Gastroenterol Hepatol. 2016 Feb;31(2):403-8. doi: 10.1111/jgh.13071.

PMID:
26250421
16.

[A case of unconjugated hyperbilirubinemia: Gilbert's syndrome or type II Crigler-Najjar syndrome?].

Heredia Centeno ML, Gómez Rodríguez R, Hernández Guío C.

Rev Clin Esp. 1987 May;180(9):502-3. Spanish. No abstract available.

PMID:
3616040
17.

Gilbert-Meulengracht's syndrome and pharmacogenetics: is jaundice just the tip of the iceberg?

Strassburg CP.

Drug Metab Rev. 2010 Feb;42(1):168-81. doi: 10.3109/03602530903209429.

PMID:
20070246
18.
19.

Inherited disorders of bilirubin metabolism.

Bosma PJ.

J Hepatol. 2003 Jan;38(1):107-17. Review. No abstract available.

PMID:
12480568
20.

Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes.

Sampietro M, Iolascon A.

Haematologica. 1999 Feb;84(2):150-7. Review.

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