Weiss KH - Search Results

1

Iron metabolism and the role of HFE gene polymorphisms in Wilson disease.

Pfeiffenberger J, Gotthardt DN, Herrmann T, Seessle J, Merle U, Schirmacher P, Stremmel W, Weiss KH. Pfeiffenberger J, et al. Among authors: weiss kh. Liver Int. 2012 Jan;32(1):165-70. doi: 10.1111/j.1478-3231.2011.02661.x. Epub 2011 Oct 17. Liver Int. 2012. PMID: 22098612

2

Copper toxicosis gene MURR1 is not changed in Wilson disease patients with normal blood ceruloplasmin levels.

Weiss KH, Merle U, Schaefer M, Ferenci P, Fullekrug J, Stremmel W. Weiss KH, et al. World J Gastroenterol. 2006 Apr 14;12(14):2239-42. doi: 10.3748/wjg.v12.i14.2239. World J Gastroenterol. 2006. PMID: 16610028 Free PMC article.

3

Prophylaxis and treatment of recurrent viral hepatitis after liver transplantation.

Riediger C, Berberat PO, Sauer P, Gotthardt D, Weiss KH, Mehrabi A, Merle U, Stremmel W, Encke J. Riediger C, et al. Among authors: weiss kh. Nephrol Dial Transplant. 2007 Sep;22 Suppl 8:viii37-viii46. doi: 10.1093/ndt/gfm655. Nephrol Dial Transplant. 2007. PMID: 17890261 Review.

4

Fulminant hepatic failure: etiology and indications for liver transplantation.

Gotthardt D, Riediger C, Weiss KH, Encke J, Schemmer P, Schmidt J, Sauer P. Gotthardt D, et al. Among authors: weiss kh. Nephrol Dial Transplant. 2007 Sep;22 Suppl 8:viii5-viii8. doi: 10.1093/ndt/gfm650. Nephrol Dial Transplant. 2007. PMID: 17890263 Review.

5

Liver transplantation for metabolic liver diseases in adults: indications and outcome.

Weiss KH, Gotthardt D, Schmidt J, Schemmer P, Encke J, Riediger C, Stremmel W, Sauer P, Merle U. Weiss KH, et al. Nephrol Dial Transplant. 2007 Sep;22 Suppl 8:viii9-viii12. doi: 10.1093/ndt/gfm658. Nephrol Dial Transplant. 2007. PMID: 17890269 Review.

6

Wilson protein expression, copper excretion and sweat production in sweat glands of Wilson disease patients and controls.

Schaefer M, Schellenberg M, Merle U, Weiss KH, Stremmel W. Schaefer M, et al. Among authors: weiss kh. BMC Gastroenterol. 2008 Jul 17;8:29. doi: 10.1186/1471-230X-8-29. BMC Gastroenterol. 2008. PMID: 18637198 Free PMC article.

7

Localization of the Wilson disease protein in murine intestine.

Weiss KH, Wurz J, Gotthardt D, Merle U, Stremmel W, Füllekrug J. Weiss KH, et al. J Anat. 2008 Sep;213(3):232-40. doi: 10.1111/j.1469-7580.2008.00954.x. Epub 2008 Jul 25. J Anat. 2008. PMID: 18673401 Free PMC article.

8

A mutation in the canalicular phospholipid transporter gene, ABCB4, is associated with cholestasis, ductopenia, and cirrhosis in adults.

Gotthardt D, Runz H, Keitel V, Fischer C, Flechtenmacher C, Wirtenberger M, Weiss KH, Imparato S, Braun A, Hemminki K, Stremmel W, Rüschendorf F, Stiehl A, Kubitz R, Burwinkel B, Schirmacher P, Knisely AS, Zschocke J, Sauer P. Gotthardt D, et al. Among authors: weiss kh. Hepatology. 2008 Oct;48(4):1157-66. doi: 10.1002/hep.22485. Hepatology. 2008. PMID: 18781607

9

Copper-induced translocation of the Wilson disease protein ATP7B independent of Murr1/COMMD1 and Rab7.

Weiss KH, Lozoya JC, Tuma S, Gotthardt D, Reichert J, Ehehalt R, Stremmel W, Füllekrug J. Weiss KH, et al. Am J Pathol. 2008 Dec;173(6):1783-94. doi: 10.2353/ajpath.2008.071134. Epub 2008 Oct 30. Am J Pathol. 2008. PMID: 18974300 Free PMC article.

10

Serum ceruloplasmin oxidase activity is a sensitive and highly specific diagnostic marker for Wilson's disease.

Merle U, Eisenbach C, Weiss KH, Tuma S, Stremmel W. Merle U, et al. Among authors: weiss kh. J Hepatol. 2009 Nov;51(5):925-30. doi: 10.1016/j.jhep.2009.06.022. Epub 2009 Jul 30. J Hepatol. 2009. PMID: 19720421

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