Similar articles for PMID: 12601343

Year	Number of Results
1998	2
2001	1
2002	2
2003	8
2004	4
2005	4
2006	6
2007	7
2008	8
2009	2
2010	1
2011	3
2012	1
2013	1
2014	1
2015	1
2021	1
2024	0

1

Genetic polymorphisms and the progression of liver fibrosis: a critical appraisal.

Bataller R, North KE, Brenner DA. Bataller R, et al. Hepatology. 2003 Mar;37(3):493-503. doi: 10.1053/jhep.2003.50127. Hepatology. 2003. PMID: 12601343 Review.

2

[Genetic risk factors for hepatic fibrosis in chronic liver diseases].

Wasmuth HE, Lammert F, Matern S. Wasmuth HE, et al. Med Klin (Munich). 2003 Dec 15;98(12):754-62. doi: 10.1007/s00063-003-1324-3. Med Klin (Munich). 2003. PMID: 14685677 Review. German.

3

Common heterozygous hemochromatosis gene mutations are risk factors for inflammation and fibrosis in chronic hepatitis C.

Geier A, Reugels M, Weiskirchen R, Wasmuth HE, Dietrich CG, Siewert E, Gartung C, Lorenzen J, Bosserhoff AK, Brügmann M, Gressner AM, Matern S, Lammert F. Geier A, et al. Liver Int. 2004 Aug;24(4):285-94. doi: 10.1111/j.1478-3231.2004.0928.x. Liver Int. 2004. PMID: 15287851

4

[Genetic polymorphisms and liver diseases].

Bataller R. Bataller R. Gastroenterol Hepatol. 2003 May;26(5):307-9. doi: 10.1016/s0210-5705(03)70363-x. Gastroenterol Hepatol. 2003. PMID: 12732105 Spanish. No abstract available.

5

[Genome-wide association studies in hepatology].

Weber S, Grünhage F, Hall R, Lammert F. Weber S, et al. Z Gastroenterol. 2010 Jan;48(1):56-64. doi: 10.1055/s-0028-1109982. Epub 2010 Jan 13. Z Gastroenterol. 2010. PMID: 20072997 Review. German.

6

The HFE gene heterozygosis H63D: a cofactor for liver damage in patients with steatohepatitis? Epidemiological and clinical considerations.

Neri S, Pulvirenti D, Signorelli S, Ignaccolo L, Tsami A, Mauceri B, Misseri M, Interlandi D, Cutuli N, Castellino P. Neri S, et al. Intern Med J. 2008 Apr;38(4):254-8. doi: 10.1111/j.1445-5994.2007.01474.x. Epub 2007 Oct 3. Intern Med J. 2008. PMID: 17916170

7

HFE mutations, hepatic iron, and fibrosis: ethnic-specific association of NASH with C282Y but not with fibrotic severity.

Chitturi S, Weltman M, Farrell GC, McDonald D, Kench J, Liddle C, Samarasinghe D, Lin R, Abeygunasekera S, George J. Chitturi S, et al. Hepatology. 2002 Jul;36(1):142-9. doi: 10.1053/jhep.2002.33892. Hepatology. 2002. PMID: 12085358

8

Hepatic iron overload in patients with chronic viral hepatitis: role of HFE gene mutations.

Piperno A, Vergani A, Malosio I, Parma L, Fossati L, Ricci A, Bovo G, Boari G, Mancia G. Piperno A, et al. Hepatology. 1998 Oct;28(4):1105-9. doi: 10.1002/hep.510280427. Hepatology. 1998. PMID: 9755249

9

HFE mutations in nonalcoholic fatty liver disease.

Valenti L, Dongiovanni P, Fracanzani AL, Fargion S. Valenti L, et al. Hepatology. 2008 May;47(5):1794-5; author reply 1795-6. doi: 10.1002/hep.22059. Hepatology. 2008. PMID: 18438784 No abstract available.

10

Heterozygosity for hereditary hemochromatosis is associated with more fibrosis in chronic hepatitis C.

Smith BC, Gorve J, Guzail MA, Day CP, Daly AK, Burt AD, Bassendine MF. Smith BC, et al. Hepatology. 1998 Jun;27(6):1695-9. doi: 10.1002/hep.510270631. Hepatology. 1998. PMID: 9620344

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