Weiss KH - Search Results

1

Wilson's disease and other neurological copper disorders.

Bandmann O, Weiss KH, Kaler SG. Bandmann O, et al. Among authors: weiss kh. Lancet Neurol. 2015 Jan;14(1):103-13. doi: 10.1016/S1474-4422(14)70190-5. Lancet Neurol. 2015. PMID: 25496901 Free PMC article. Review.

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

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.

4

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.

5

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.

6

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

7

Truncating mutations in the Wilson disease gene ATP7B are associated with very low serum ceruloplasmin oxidase activity and an early onset of Wilson disease.

Merle U, Weiss KH, Eisenbach C, Tuma S, Ferenci P, Stremmel W. Merle U, et al. Among authors: weiss kh. BMC Gastroenterol. 2010 Jan 18;10:8. doi: 10.1186/1471-230X-10-8. BMC Gastroenterol. 2010. PMID: 20082719 Free PMC article.

8

Genetic analysis of BIRC4/XIAP as a putative modifier gene of Wilson disease.

Weiss KH, Runz H, Noe B, Gotthardt DN, Merle U, Ferenci P, Stremmel W, Füllekrug J. Weiss KH, et al. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S233-40. doi: 10.1007/s10545-010-9123-5. Epub 2010 Jun 2. J Inherit Metab Dis. 2010. PMID: 20517649

9

Evaluation of the symptomatic treatment of residual neurological symptoms in Wilson disease.

Hölscher S, Leinweber B, Hefter H, Reuner U, Günther P, Weiss KH, Oertel WH, Möller JC. Hölscher S, et al. Among authors: weiss kh. Eur Neurol. 2010;64(2):83-7. doi: 10.1159/000316066. Epub 2010 Jul 6. Eur Neurol. 2010. PMID: 20606453

10

Alterations of lipid metabolism in Wilson disease.

Seessle J, Gohdes A, Gotthardt DN, Pfeiffenberger J, Eckert N, Stremmel W, Reuner U, Weiss KH. Seessle J, et al. Among authors: weiss kh. Lipids Health Dis. 2011 May 19;10:83. doi: 10.1186/1476-511X-10-83. Lipids Health Dis. 2011. PMID: 21595966 Free PMC article.

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