Literature DB >> 3943418

Clinical features in familial polyposis coli. Results of the Danish Polyposis Register.

S Bülow.   

Abstract

Three hundred nineteen affected members of 94 Danish families with familial polyposis coli had been registered in the Danish Polyposis Register by the end of 1982. Of the 247 histologically verified cases, 168 were propositi and 79 were call-up patients. The frequency of colorectal cancer at the time of diagnosis of polyposis was 69 percent in propositi vs. 3 percent in call-up patients. The cumulative survival rate after ten years was 97 percent in call-up patients, as compared to 42 percent in propositi. The prognosis of polyposis patients has improved significantly since the establishment of the Danish Polyposis Register in 1971.

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Year:  1986        PMID: 3943418     DOI: 10.1007/bf02555389

Source DB:  PubMed          Journal:  Dis Colon Rectum        ISSN: 0012-3706            Impact factor:   4.585


  23 in total

Review 1.  [Carcinogenesis and hereditart colon cancers].

Authors:  F Kullmann
Journal:  Internist (Berl)       Date:  2003-03       Impact factor: 0.743

Review 2.  The history of familial adenomatous polyposis.

Authors:  Steffen Bülow; Terri Berk; Kay Neale
Journal:  Fam Cancer       Date:  2006       Impact factor: 2.375

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

Authors:  Constanze Pagenstecher; Dorothea Gadzicki; Dietlinde Stienen; Siegfried Uhlhaas; Elisabeth Mangold; Nils Rahner; Mine Arslan-Kirchner; Peter Propping; Waltraut Friedl; Stefan Aretz
Journal:  J Mol Diagn       Date:  2007-02       Impact factor: 5.568

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

Authors:  W Friedl; R Caspari; M Sengteller; S Uhlhaas; C Lamberti; M Jungck; M Kadmon; M Wolf; J Fahnenstich; J Gebert; G Möslein; E Mangold; P Propping
Journal:  Gut       Date:  2001-04       Impact factor: 23.059

5.  Familial adenomatous polyposis in a 5 year old child: a clinical, pathological, and molecular genetic study.

Authors:  S Distante; S Nasioulas; G R Somers; D J Cameron; M A Young; S M Forrest; R J Gardner
Journal:  J Med Genet       Date:  1996-02       Impact factor: 6.318

6.  Prevalence of skin lesions in familial adenomatous polyposis: a marker for presymptomatic diagnosis?

Authors:  Bettina Burger; Nadja Cattani; Swantje Trueb; Rosaria de Lorenzo; Mauro Albertini; Emanuele Bontognali; Christoph Itin; Nathalie Schaub; Peter H Itin; Karl Heinimann
Journal:  Oncologist       Date:  2011-12-01

7.  Diagnosis of familial adenomatous polyposis.

Authors:  S Bülow
Journal:  World J Surg       Date:  1991 Jan-Feb       Impact factor: 3.352

8.  APC mutation spectrum of Norwegian familial adenomatous polyposis families: high ratio of novel mutations.

Authors:  Per Arne Andresen; Ketil Heimdal; Kristin Aaberg; Katrine Eklo; Kristin Eklo; Sarah Ariansen; Alexandra Silye; Olav Fausa; Lars Aabakken; Stefan Aretz; Tor J Eide; Tobias Gedde-Dahl
Journal:  J Cancer Res Clin Oncol       Date:  2009-05-15       Impact factor: 4.553

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

Authors:  Waltraut Friedl; Stefan Aretz
Journal:  Hered Cancer Clin Pract       Date:  2005-09-15       Impact factor: 2.857

10.  Rectal and pouch recurrences after surgical treatment for familial adenomatous polyposis.

Authors:  Fabio Guilherme Campos; Antonio Rocco Imperiale; Víctor Edmond Seid; Rodrigo Oliva Perez; Afonso Henrique da Silva e Sousa; Desidério Roberto Kiss; Angelita Habr-Gama; Ivan Cecconello
Journal:  J Gastrointest Surg       Date:  2008-09-03       Impact factor: 3.452

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