Aretz S - Search Results

1

Early detection of duodenal cancer by upper gastrointestinal-endoscopy in Lynch syndrome.

Vangala DB, Ladigan-Badura S, Engel C, Hüneburg R, Perne C, Bucksch K, Nattermann J, Steinke-Lange V, Rahner N, Weitz J, Kloor M, Tomann J, Canbay A, Nguyen HP, Strassburg C, Möslein G, Morak M, Holinski-Feder E, Büttner R, Aretz S, Löffler M, Schmiegel W, Pox C, Schulmann K; German Consortium for Familial Intestinal Cancer. Vangala DB, et al. Among authors: aretz s. Int J Cancer. 2021 Dec 15;149(12):2052-2062. doi: 10.1002/ijc.33753. Epub 2021 Aug 7. Int J Cancer. 2021. PMID: 34331771

2

MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?

Mangold E, Rahner N, Friedrichs N, Buettner R, Pagenstecher C, Aretz S, Friedl W, Ruzicka T, Propping P, Rütten A, Kruse R. Mangold E, et al. Among authors: aretz s. Br J Dermatol. 2007 Jan;156(1):158-62. doi: 10.1111/j.1365-2133.2006.07607.x. Br J Dermatol. 2007. PMID: 17199584 No abstract available.

3

A complex rearrangement in the APC gene uncovered by multiplex ligation-dependent probe amplification.

Pagenstecher C, Gadzicki D, Stienen D, Uhlhaas S, Mangold E, Rahner N, Arslan-Kirchner M, Propping P, Friedl W, Aretz S. Pagenstecher C, et al. Among authors: aretz s. J Mol Diagn. 2007 Feb;9(1):122-6. doi: 10.2353/jmoldx.2007.060096. J Mol Diagn. 2007. PMID: 17251345 Free PMC article.

4

Nine novel pathogenic germline mutations in MLH1, MSH2, MSH6 and PMS2 in families with Lynch syndrome.

Rahner N, Friedrichs N, Wehner M, Steinke V, Aretz S, Friedl W, Buettner R, Mangold E, Propping P, Walldorf C. Rahner N, et al. Among authors: aretz s. Acta Oncol. 2007;46(6):763-9. doi: 10.1080/02841860701230217. Acta Oncol. 2007. PMID: 17653898

5

Association of familial colorectal cancer with variants in the E-cadherin (CDH1) and cyclin D1 (CCND1) genes.

Grünhage F, Jungck M, Lamberti C, Berg C, Becker U, Schulte-Witte H, Plassmann D, Rahner N, Aretz S, Friedrichs N, Buettner R, Sauerbruch T, Lammert F. Grünhage F, et al. Among authors: aretz s. Int J Colorectal Dis. 2008 Feb;23(2):147-54. doi: 10.1007/s00384-007-0388-6. Epub 2007 Oct 25. Int J Colorectal Dis. 2008. PMID: 17960397

6

Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndrome.

Rahner N, Friedrichs N, Steinke V, Aretz S, Friedl W, Buettner R, Mangold E, Propping P, Walldorf C. Rahner N, et al. Among authors: aretz s. J Pathol. 2008 Jan;214(1):10-6. doi: 10.1002/path.2263. J Pathol. 2008. PMID: 17973250

7

No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients.

Steinke V, Rahner N, Morak M, Keller G, Schackert HK, Görgens H, Schmiegel W, Royer-Pokora B, Dietmaier W, Kloor M, Engel C, Propping P, Aretz S; German HNPCC Consortium. Steinke V, et al. Among authors: aretz s. Eur J Hum Genet. 2008 May;16(5):587-92. doi: 10.1038/ejhg.2008.26. Epub 2008 Feb 27. Eur J Hum Genet. 2008. PMID: 18301448

8

Compound heterozygosity for two MSH6 mutations in a patient with early onset colorectal cancer, vitiligo and systemic lupus erythematosus.

Rahner N, Höefler G, Högenauer C, Lackner C, Steinke V, Sengteller M, Friedl W, Aretz S, Propping P, Mangold E, Walldorf C. Rahner N, et al. Among authors: aretz s. Am J Med Genet A. 2008 May 15;146A(10):1314-9. doi: 10.1002/ajmg.a.32210. Am J Med Genet A. 2008. PMID: 18409202 Review.

9

Contribution of common monoallelic MUTYH gene variants in German patients with familial colorectal cancer.

Grünhage F, Jungck M, Lamberti C, Schulte-Witte H, Plassmann D, Becker U, Rahner N, Aretz S, Friedrichs N, Buettner R, Sauerbruch T, Lammert F. Grünhage F, et al. Among authors: aretz s. Cancer Biomark. 2008;4(2):55-61. doi: 10.3233/cbm-2008-4201. Cancer Biomark. 2008. PMID: 18503156

10

Truncating mutations in Peutz-Jeghers syndrome are associated with more polyps, surgical interventions and cancers.

Salloch H, Reinacher-Schick A, Schulmann K, Pox C, Willert J, Tannapfel A, Heringlake S, Goecke TO, Aretz S, Stemmler S, Schmiegel W. Salloch H, et al. Among authors: aretz s. Int J Colorectal Dis. 2010 Jan;25(1):97-107. doi: 10.1007/s00384-009-0793-0. Epub 2009 Sep 2. Int J Colorectal Dis. 2010. PMID: 19727776

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