Related Articles by Review for PMID: 31747203

Year	Number of Results
1994	1
1999	1
2000	1
2002	2
2003	1
2005	2
2006	1
2007	1
2009	2
2010	1
2013	1
2014	3
2015	3
2016	1
2017	2
2018	1
2023	1
2025	1

1

Singh A, Koritala T, Jialal I. Singh A, et al. 2023 Feb 20. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2023 Feb 20. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 31747203 Free Books & Documents.

2

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. Kadakol A, et al. Hum Mutat. 2000 Oct;16(4):297-306. doi: 10.1002/1098-1004(200010)16:4<297::AID-HUMU2>3.0.CO;2-Z. Hum Mutat. 2000. PMID: 11013440 Review.

3

Gene replacement therapy for genetic hepatocellular jaundice.

van Dijk R, Beuers U, Bosma PJ. van Dijk R, et al. Clin Rev Allergy Immunol. 2015 Jun;48(2-3):243-53. doi: 10.1007/s12016-014-8454-7. Clin Rev Allergy Immunol. 2015. PMID: 25315738 Review.

4

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

Sampietro M, Iolascon A. Sampietro M, et al. Haematologica. 1999 Feb;84(2):150-7. Haematologica. 1999. PMID: 10091414 Review.

5

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

Erlinger S, Arias IM, Dhumeaux D. Erlinger S, et al. Gastroenterology. 2014 Jun;146(7):1625-38. doi: 10.1053/j.gastro.2014.03.047. Epub 2014 Apr 1. Gastroenterology. 2014. PMID: 24704527 Review.

6

Metalloporphyrins for treatment of unconjugated hyperbilirubinemia in neonates.

Suresh GK, Martin CL, Soll RF. Suresh GK, et al. Cochrane Database Syst Rev. 2003;(2):CD004207. doi: 10.1002/14651858.CD004207. Cochrane Database Syst Rev. 2003. PMID: 12804504 Review.

7

Inherited disorders of bilirubin clearance.

Memon N, Weinberger BI, Hegyi T, Aleksunes LM. Memon N, et al. Pediatr Res. 2016 Mar;79(3):378-86. doi: 10.1038/pr.2015.247. Epub 2015 Nov 23. Pediatr Res. 2016. PMID: 26595536 Free PMC article. Review.

8

[Inherited disorders of bilirubin metabolism].

Rossi F, Francese M, Iodice RM, Falcone E, Vetrella S, Punzo F, De Vita S, Perrotta S. Rossi F, et al. Minerva Pediatr. 2005 Apr;57(2):53-63. Minerva Pediatr. 2005. PMID: 15985997 Review. Italian.

9

[From gene to disease; unconjugated hyperbilirubinemia: Gilbert's syndrome and Crigler-Najjar types I and II].

Drenth JP, Peters WH, Jansen JB. Drenth JP, et al. Ned Tijdschr Geneeskd. 2002 Aug 10;146(32):1488-90. Ned Tijdschr Geneeskd. 2002. PMID: 12198827 Review. Dutch.

10

Diagnostic criteria and contributors to Gilbert's syndrome.

Wagner KH, Shiels RG, Lang CA, Seyed Khoei N, Bulmer AC. Wagner KH, et al. Crit Rev Clin Lab Sci. 2018 Mar;55(2):129-139. doi: 10.1080/10408363.2018.1428526. Epub 2018 Feb 1. Crit Rev Clin Lab Sci. 2018. PMID: 29390925 Free article. Review.

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