Similar articles for PMID: 31582009

Year	Number of Results
1987	1
1989	1
1990	1
1995	1
1996	2
1997	3
1998	4
1999	2
2000	1
2001	2
2002	3
2004	5
2005	5
2006	2
2007	2
2008	4
2009	2
2010	5
2011	1
2012	3
2013	2
2014	2
2015	5
2016	3
2017	6
2018	4
2019	1
2020	2
2021	3
2022	1
2024	0

1

Genetic Causes of Liver Disease: When to Suspect a Genetic Etiology, Initial Lab Testing, and the Basics of Management.

Schonfeld EA, Brown RS Jr. Schonfeld EA, et al. Med Clin North Am. 2019 Nov;103(6):991-1003. doi: 10.1016/j.mcna.2019.07.003. Med Clin North Am. 2019. PMID: 31582009 Review.

2

Genetic Testing in Liver Disease: What to Order, in Whom, and When.

Schonfeld EA, Brown RS Jr. Schonfeld EA, et al. Clin Liver Dis. 2017 Nov;21(4):673-686. doi: 10.1016/j.cld.2017.06.001. Epub 2017 Jul 29. Clin Liver Dis. 2017. PMID: 28987255 Review.

3

Characterization of mutations in ATP8B1 associated with hereditary cholestasis.

Klomp LW, Vargas JC, van Mil SW, Pawlikowska L, Strautnieks SS, van Eijk MJ, Juijn JA, Pabón-Peña C, Smith LB, DeYoung JA, Byrne JA, Gombert J, van der Brugge G, Berger R, Jankowska I, Pawlowska J, Villa E, Knisely AS, Thompson RJ, Freimer NB, Houwen RH, Bull LN. Klomp LW, et al. Hepatology. 2004 Jul;40(1):27-38. doi: 10.1002/hep.20285. Hepatology. 2004. PMID: 15239083

4

Progressive familial intrahepatic cholestasis and benign recurrent intrahepatic cholestasis: a review.

Strubbe B, Geerts A, Van Vlierberghe H, Colle I. Strubbe B, et al. Acta Gastroenterol Belg. 2012 Dec;75(4):405-10. Acta Gastroenterol Belg. 2012. PMID: 23402083 Free article. Review.

5

[Diagnosis and therapy of inheritable liver diseases: hemochromatisis, Wilson's disease and alpha-1-antitrypsin deficiency].

Strassburg ChP. Strassburg ChP. Praxis (Bern 1994). 2005 Jan 19;94(3):73-81. doi: 10.1024/0369-8394.94.3.73. Praxis (Bern 1994). 2005. PMID: 15719801 German.

6

[Benign recurrent intrahepatic cholestasis type-II--a rare cause of direct hyperbilirubinemia exacerbations with hepatic fibrosis].

Mizrahi M, Lalazar G, Horwich Y, Adar T, Safadi R. Mizrahi M, et al. Harefuah. 2008 May;147(5):381-3, 480. Harefuah. 2008. PMID: 18770956 Hebrew.

7

Progressive familial intrahepatic cholestasis.

Cavestro GM, Frulloni L, Cerati E, Ribeiro LA, Corrente V, Sianesi M, Franzè A, Di Mario F. Cavestro GM, et al. Acta Biomed. 2002;73(3-4):53-6. Acta Biomed. 2002. PMID: 12596388 Review.

8

Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11.

van Mil SW, van der Woerd WL, van der Brugge G, Sturm E, Jansen PL, Bull LN, van den Berg IE, Berger R, Houwen RH, Klomp LW. van Mil SW, et al. Gastroenterology. 2004 Aug;127(2):379-84. doi: 10.1053/j.gastro.2004.04.065. Gastroenterology. 2004. PMID: 15300568

9

Familial cholestasis: progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy.

van der Woerd WL, van Mil SW, Stapelbroek JM, Klomp LW, van de Graaf SF, Houwen RH. van der Woerd WL, et al. Best Pract Res Clin Gastroenterol. 2010 Oct;24(5):541-53. doi: 10.1016/j.bpg.2010.07.010. Best Pract Res Clin Gastroenterol. 2010. PMID: 20955958 Review.

10

Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region.

Carlton VE, Knisely AS, Freimer NB. Carlton VE, et al. Hum Mol Genet. 1995 Jun;4(6):1049-53. doi: 10.1093/hmg/4.6.1049. Hum Mol Genet. 1995. PMID: 7655458

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