Heinimann K - Search Results

1

Detection of APC germ line mosaicism in patients with de novo familial adenomatous polyposis: a plea for the protein truncation test.

Necker J, Kovac M, Attenhofer M, Reichlin B, Heinimann K. Necker J, et al. Among authors: heinimann k. J Med Genet. 2011 Aug;48(8):526-9. doi: 10.1136/jmg.2011.089474. Epub 2011 Jun 7. J Med Genet. 2011. PMID: 21653199

2

Identification of a modifier gene locus on chromosome 1p35-36 in familial adenomatous polyposis.

Dobbie Z, Heinimann K, Bishop DT, Müller H, Scott RJ. Dobbie Z, et al. Among authors: heinimann k. Hum Genet. 1997 May;99(5):653-7. doi: 10.1007/s004390050423. Hum Genet. 1997. PMID: 9150735

3

Association of extracolonic manifestations of familial adenomatous polyposis with acetylation phenotype in a large FAP kindred.

Scott RJ, Taeschner W, Heinimann K, Müller H, Dobbie Z, Morgenthaler S, Hoffmann F, Peterli B, Meyer UA. Scott RJ, et al. Among authors: heinimann k. Eur J Hum Genet. 1997 Jan-Feb;5(1):43-9. Eur J Hum Genet. 1997. PMID: 9156320

4

Phenotypic differences in familial adenomatous polyposis based on APC gene mutation status.

Heinimann K, Müllhaupt B, Weber W, Attenhofer M, Scott RJ, Fried M, Martinoli S, Müller H, Dobbie Z. Heinimann K, et al. Gut. 1998 Nov;43(5):675-9. doi: 10.1136/gut.43.5.675. Gut. 1998. PMID: 9824350 Free PMC article.

5

Influence of selection criteria on mutation detection in patients with hereditary nonpolyposis colorectal cancer.

Heinimann K, Scott RJ, Buerstedde JM, Weber W, Siebold K, Attenhofer M, Müller H, Dobbie Z. Heinimann K, et al. Cancer. 1999 Jun 15;85(12):2512-8. doi: 10.1002/(sici)1097-0142(19990615)85:12<2512::aid-cncr4>3.0.co;2-g. Cancer. 1999. PMID: 10375096

6

[Early diagnosis of familial adenomatous polyposis based on multiple osteomas of the facial skull].

Heinimann K, Kunz C, Farine E, Rey JP, Müller H, Dobbie Z. Heinimann K, et al. Schweiz Med Wochenschr. 1999 May 1;129(17):665-9. Schweiz Med Wochenschr. 1999. PMID: 10407937 German.

7

Nontruncating APC germ-line mutations and mismatch repair deficiency play a minor role in APC mutation-negative polyposis.

Heinimann K, Thompson A, Locher A, Furlanetto T, Bader E, Wolf A, Meier R, Walter K, Bauerfeind P, Marra G, Müller H, Foernzler D, Dobbie Z. Heinimann K, et al. Cancer Res. 2001 Oct 15;61(20):7616-22. Cancer Res. 2001. PMID: 11606402

8

Expression of COX-2 and Wnt pathway genes in adenomas of familial adenomatous polyposis patients treated with meloxicam.

Dobbie Z, Muller PY, Heinimann K, Albrecht C, D'Orazio D, Bendik I, Müller H, Bauerfeind P. Dobbie Z, et al. Among authors: heinimann k. Anticancer Res. 2002 Jul-Aug;22(4):2215-20. Anticancer Res. 2002. PMID: 12174906

9

Overexpression of Wnt target genes in adenomas of familial adenomatous polyposis patients.

D'Orazio D, Muller PY, Heinimann K, Albrecht C, Bendik I, Herzog U, Tondelli P, Bauerfeind P, Müller H, Dobbie Z. D'Orazio D, et al. Among authors: heinimann k. Anticancer Res. 2002 Nov-Dec;22(6A):3409-14. Anticancer Res. 2002. PMID: 12530096

10

Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH.

Sieber OM, Lipton L, Crabtree M, Heinimann K, Fidalgo P, Phillips RK, Bisgaard ML, Orntoft TF, Aaltonen LA, Hodgson SV, Thomas HJ, Tomlinson IP. Sieber OM, et al. Among authors: heinimann k. N Engl J Med. 2003 Feb 27;348(9):791-9. doi: 10.1056/NEJMoa025283. N Engl J Med. 2003. PMID: 12606733 Free article.

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