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Items: 1 to 20 of 102

1.

Multiple liver lesions of unusual benign etiology mimicking metastatic disease.

Pais TP, Fernandes S, Fraga J.

Gastroenterology. 2014 Aug;147(2):e10-1. doi: 10.1053/j.gastro.2014.03.039. Epub 2014 Jun 25. No abstract available.

PMID:
24973686
2.

The role of iron in nonalcoholic fatty liver disease: the story continues.

Kowdley KV.

Gastroenterology. 2010 Mar;138(3):817-9. doi: 10.1053/j.gastro.2010.01.023. Epub 2010 Jan 28. No abstract available.

PMID:
20116466
3.

A patient with a rare cause of elevated troponin I.

Kilias A, Klingel K, Gawaz M, Kramer U, Seizer P.

Clin Res Cardiol. 2015 Sep;104(9):794-7. doi: 10.1007/s00392-015-0864-x. Epub 2015 Apr 28. No abstract available.

PMID:
25916738
4.

Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosis.

Valenti L, Maggioni P, Piperno A, Rametta R, Pelucchi S, Mariani R, Dongiovanni P, Fracanzani AL, Fargion S.

World J Gastroenterol. 2012 Jun 14;18(22):2813-20. doi: 10.3748/wjg.v18.i22.2813.

5.

HFE genotyping: maximising the value for hemochromatosis patients and families.

Bassett ML.

J Gastroenterol Hepatol. 2010 Jul;25(7):1186-8. doi: 10.1111/j.1440-1746.2010.06387.x. No abstract available.

PMID:
20594244
6.

Multifocal nodular fatty infiltration of the liver mimicking metastatic liver tumors: diagnosis using the liver-specific late phase of Levovist-enhanced sonography.

Tamai H, Shingaki N, Oka M, Shiraki T, Inoue I, Magari H, Fujishiro M, Iguchi M, Yanaoka K, Arii K, Shimizu Y, Ichinose M.

J Ultrasound Med. 2006 Mar;25(3):403-6. No abstract available.

PMID:
16495505
7.

HFE genotype, parenchymal iron accumulation, and liver fibrosis in patients with nonalcoholic fatty liver disease.

Valenti L, Fracanzani AL, Bugianesi E, Dongiovanni P, Galmozzi E, Vanni E, Canavesi E, Lattuada E, Roviaro G, Marchesini G, Fargion S.

Gastroenterology. 2010 Mar;138(3):905-12. doi: 10.1053/j.gastro.2009.11.013. Epub 2009 Nov 18.

8.

Usefulness of Magnetic Resonance Imaging for the Diagnosis of Hemochromatosis with Severe Hepatic Steatosis in Nonalcoholic Fatty Liver Disease.

Nozaki Y, Sato N, Tajima T, Hasuo K, Kojima Y, Umemoto K, Mishima S, Mikami S, Nakayama T, Igari T, Akiyama J, Imamura M, Masaki N, Yanase M.

Intern Med. 2016;55(17):2413-7. doi: 10.2169/internalmedicine.55.6650. Epub 2016 Sep 1.

9.

[Heterozygosis H63D in patients with steatohepatitis and chronic hepatitis C].

Pulvirenti D, Neri S, Bertino G, Cutuli N, Ignaccolo L, Misseri M, Tsami A, Caruso L.

Clin Ter. 2006 Nov-Dec;157(6):485-8. Italian.

PMID:
17228846
10.

Iron overload and HFE gene mutations in Polish patients with liver cirrhosis.

Sikorska K, Romanowski T, Stalke P, Iżycka-Świeszewska E, Bielawski KP.

Hepatobiliary Pancreat Dis Int. 2011 Jun;10(3):270-5.

PMID:
21669570
11.

[Hereditary hemochromatosis].

Niederau C.

Med Klin (Munich). 2009 Dec 15;104(12):931-46. doi: 10.1007/s00063-009-1192-6. Review. German.

PMID:
20039160
12.

Case report of a patient with non-alcoholic fatty liver disease, moderate iron overload who is homozygous for the S65C mutation in the HFE1 gene.

Bernard PH, Ged C, Faivre E, Legac G, Bioulac-Sage P, Cassaigne A, de Verneuil H.

Eur J Med Genet. 2005 Apr-Jun;48(2):195-8. Epub 2005 Feb 12. No abstract available.

PMID:
16053912
13.

An unusual case of hemochromatosis in an African-American man: case report and review of the literature.

Labowitz DA, Bontreger J, Min AD.

Dig Dis Sci. 2007 Dec;52(12):3519-20. Epub 2007 Apr 10. No abstract available.

PMID:
17420932
14.

HFE mutations analysis of Turkish patients with nonalcoholic steatohepatitis.

Simsek H, Balaban YH, Sümer H, Yilmaz E, Tatar G.

Dig Dis Sci. 2006 Oct;51(10):1723-4. No abstract available.

PMID:
16964543
15.

[Liver pathology in patients with primary hemochromatosis--homozygous carriers of C282Y mutation ].

Smirnov OA, Shneĭder OV, Radchenko VG, Nilova VK, Okon EE, Kudriavtsev BN, Saburova GS, Mitrofanov NA, Stanzhevskiĭ AA.

Arkh Patol. 2003 Jul-Aug;65(4):51-5. Russian.

PMID:
14518196
16.

Increased susceptibility to nonalcoholic fatty liver disease in heterozygotes for the mutation responsible for hereditary hemochromatosis.

Valenti L, Dongiovanni P, Fracanzani AL, Santorelli G, Fatta E, Bertelli C, Taioli E, Fiorelli G, Fargion S.

Dig Liver Dis. 2003 Mar;35(3):172-8.

PMID:
12779071
17.

HFE mutations in nonalcoholic fatty liver disease.

Valenti L, Dongiovanni P, Fracanzani AL, Fargion S.

Hepatology. 2008 May;47(5):1794-5; author reply 1795-6. doi: 10.1002/hep.22059. No abstract available.

PMID:
18438784
18.

Significance of H63D homozygosity in a Basque population with hemochromatosis.

Castiella A, Zapata E, de Juan MD, Otazua P, Fernandez J, Zubiaurre L, Arriola JA; Gipuzkoa Hemochromatosis Group.

J Gastroenterol Hepatol. 2010 Jul;25(7):1295-8. doi: 10.1111/j.1440-1746.2010.06247.x.

PMID:
20594259
19.

Duration of hepatic iron exposure increases the risk of significant fibrosis in hereditary hemochromatosis: a new role for magnetic resonance imaging.

Olynyk JK, St Pierre TG, Britton RS, Brunt EM, Bacon BR.

Am J Gastroenterol. 2005 Apr;100(4):837-41.

PMID:
15784029
20.

Focal fatty change of the liver: cytologic findings in a radiographic mimic of metastases.

Layfield LJ.

Diagn Cytopathol. 1994 Dec;11(4):385-7; discussion 387-9.

PMID:
7895578

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