Caspari R - Search Results

1

E-cadherin expression is homogeneously reduced in adenoma from patients with familial adenomatous polyposis: an immunohistochemical study of E-cadherin, beta-catenin and cyclooxygenase-2 expression.

Jungck M, Grünhage F, Spengler U, Dernac A, Mathiak M, Caspari R, Friedl W, Sauerbruch T. Jungck M, et al. Among authors: caspari r. Int J Colorectal Dis. 2004 Sep;19(5):438-45. doi: 10.1007/s00384-003-0575-z. Epub 2004 Feb 21. Int J Colorectal Dis. 2004. PMID: 14986031

2

Arylamine N-acetyltransferase type 2 and glutathione S-transferases M1 and T1 polymorphisms in familial adenomatous polyposis.

Lamberti C, Jungck M, Laarmann M, Knapp M, Caspari R, Friedl W, Sauerbruch T, Propping P, Kruse R. Lamberti C, et al. Among authors: caspari r. Pharmacogenetics. 2002 Jan;12(1):49-54. doi: 10.1097/00008571-200201000-00007. Pharmacogenetics. 2002. PMID: 11773864

3

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: caspari r. Eur J Hum Genet. 2004 Jan;12(1):52-8. doi: 10.1038/sj.ejhg.5201088. Eur J Hum Genet. 2004. PMID: 14523376

4

Familial adenomatous polyposis: mutation at codon 1309 and early onset of colon cancer.

Caspari R, Friedl W, Mandl M, Möslein G, Kadmon M, Knapp M, Jacobasch KH, Ecker KW, Kreissler-Haag D, Timmermanns G, et al. Caspari R, et al. Lancet. 1994 Mar 12;343(8898):629-32. doi: 10.1016/s0140-6736(94)92634-4. Lancet. 1994. PMID: 7906810

5

Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposis.

Mandl M, Paffenholz R, Friedl W, Caspari R, Sengteller M, Propping P. Mandl M, et al. Among authors: caspari r. Hum Mol Genet. 1994 Jan;3(1):181-4. doi: 10.1093/hmg/3.1.181. Hum Mol Genet. 1994. PMID: 8162022

6

[Diagnosis of familial adenomatosis polyposis].

Friedl W, Caspari R, Propping P. Friedl W, et al. Among authors: caspari r. Dtsch Med Wochenschr. 1994 Jan 7;119(1-2):27-30. doi: 10.1055/s-2008-1058657. Dtsch Med Wochenschr. 1994. PMID: 8281879 Review. German. No abstract available.

7

Familial adenomatous polyposis: a submicroscopic deletion at the APC locus in a family with mentally normal patients.

Mandl M, Caspari R, Jauch A, Böker T, Raschke H, Sengteller M, Propping P, Friedl W. Mandl M, et al. Among authors: caspari r. Hum Genet. 1996 Feb;97(2):204-8. doi: 10.1007/BF02265266. Hum Genet. 1996. PMID: 8566954

8

Microsatellite instability-a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with colorectal cancer.

Lamberti C, Kruse R, Ruelfs C, Caspari R, Wang Y, Jungck M, Mathiak M, Malayeri HR, Friedl W, Sauerbruch T, Propping P. Lamberti C, et al. Among authors: caspari r. Gut. 1999 Jun;44(6):839-43. doi: 10.1136/gut.44.6.839. Gut. 1999. PMID: 10323887 Free PMC article.

9

[Therapy and after-care of familial adenomatous polyposis and hereditary colorectal carcinoma without polyposis].

Lamberti C, Jungck M, Caspari R, Schmidt-Wolf I, Sauerbruch T. Lamberti C, et al. Among authors: caspari r. Dtsch Med Wochenschr. 2000 Feb 18;125(7):189-91. doi: 10.1055/s-2007-1024018. Dtsch Med Wochenschr. 2000. PMID: 10719394 German. No abstract available.

10

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. Among authors: caspari r. Gut. 2001 Apr;48(4):515-21. doi: 10.1136/gut.48.4.515. Gut. 2001. PMID: 11247896 Free PMC article.

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