Friedl W - Search Results

1

Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?

Aretz S, Koch A, Uhlhaas S, Friedl W, Propping P, von Schweinitz D, Pietsch T. Aretz S, et al. Among authors: friedl w. Pediatr Blood Cancer. 2006 Nov;47(6):811-8. doi: 10.1002/pbc.20698. Pediatr Blood Cancer. 2006. PMID: 16317745

2

Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis.

Aretz S, Uhlhaas S, Caspari R, Mangold E, Pagenstecher C, Propping P, Friedl W. Aretz S, et al. Among authors: friedl w. Eur J Hum Genet. 2004 Jan;12(1):52-8. doi: 10.1038/sj.ejhg.5201088. Eur J Hum Genet. 2004. PMID: 14523376

3

Familial adenomatous polyposis: aberrant splicing due to missense or silent mutations in the APC gene.

Aretz S, Uhlhaas S, Sun Y, Pagenstecher C, Mangold E, Caspari R, Möslein G, Schulmann K, Propping P, Friedl W. Aretz S, et al. Among authors: friedl w. Hum Mutat. 2004 Nov;24(5):370-80. doi: 10.1002/humu.20087. Hum Mutat. 2004. PMID: 15459959

4

MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype.

Aretz S, Uhlhaas S, Goergens H, Siberg K, Vogel M, Pagenstecher C, Mangold E, Caspari R, Propping P, Friedl W. Aretz S, et al. Among authors: friedl w. Int J Cancer. 2006 Aug 15;119(4):807-14. doi: 10.1002/ijc.21905. Int J Cancer. 2006. PMID: 16557584

5

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: friedl w. J Mol Diagn. 2007 Feb;9(1):122-6. doi: 10.2353/jmoldx.2007.060096. J Mol Diagn. 2007. PMID: 17251345 Free PMC article.

6

Somatic APC mosaicism: a frequent cause of familial adenomatous polyposis (FAP).

Aretz S, Stienen D, Friedrichs N, Stemmler S, Uhlhaas S, Rahner N, Propping P, Friedl W. Aretz S, et al. Among authors: friedl w. Hum Mutat. 2007 Oct;28(10):985-92. doi: 10.1002/humu.20549. Hum Mutat. 2007. PMID: 17486639

7

Analysis of rare APC variants at the mRNA level: six pathogenic mutations and literature review.

Kaufmann A, Vogt S, Uhlhaas S, Stienen D, Kurth I, Hameister H, Mangold E, Kötting J, Kaminsky E, Propping P, Friedl W, Aretz S. Kaufmann A, et al. Among authors: friedl w. J Mol Diagn. 2009 Mar;11(2):131-9. doi: 10.2353/jmoldx.2009.080129. Epub 2009 Feb 5. J Mol Diagn. 2009. PMID: 19196998 Free PMC article. Review.

8

Familial adenomatous polyposis: experience from a study of 1164 unrelated german polyposis patients.

Friedl W, Aretz S. Friedl W, et al. Hered Cancer Clin Pract. 2005 Sep 15;3(3):95-114. doi: 10.1186/1897-4287-3-3-95. Hered Cancer Clin Pract. 2005. PMID: 20223039 Free PMC article.

9

Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families.

Friedl W, Caspari R, Sengteller M, Uhlhaas S, Lamberti C, Jungck M, Kadmon M, Wolf M, Fahnenstich J, Gebert J, Möslein G, Mangold E, Propping P. Friedl W, et al. Gut. 2001 Apr;48(4):515-21. doi: 10.1136/gut.48.4.515. Gut. 2001. PMID: 11247896 Free PMC article.

10

Analysis of germline mutations in the APC gene in familial adenomatous polyposis patients.

Liu XR, Shan XN, Friedl W, Uhlhaas S, Propping P, Wang YP. Liu XR, et al. Among authors: friedl w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Jun;22(3):261-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15952110

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

250 results

Search Page

Filters