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Hereditäres non-polypöses kolorektales Karzinom (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hereditäres non-polypöses kolorektales Karzinom" in German language version.

refsWebsite
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5doi.org
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4nih.gov
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2zdb-katalog.de
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2omim.org
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2aerzteblatt.de
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2aacrjournals.org
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1mgz-muenchen.de
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1hnpcc.de
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1web.archive.org
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1nejm.org
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aacrjournals.org

cebp.aacrjournals.org

aacrjournals.org

  • John Mathers et al.: Cancer Prevention with Resistant Starch in Lynch Syndrome Patients in the CAPP2-Randomized Placebo Controlled Trial: Planned 10-Year Follow-up. Cancer Prevention Research (25. Juli 2022)[2](Link zum PDF)

aerzteblatt.de

doi.org

  • S. Shiovitz, W. K. Copeland, M. N. Passarelli, A. N. Burnett-Hartman, W. M. Grady, J. D. Potter, S. Gallinger, D. D. Buchanan, C. Rosty, A. K. Win, M. Jenkins, S. N. Thibodeau, R. Haile, J. A. Baron, L. L. Marchand, P. A. Newcomb, N. M. Lindor: Characterisation of familial colorectal cancer Type X, Lynch syndrome, and non-familial colorectal cancer. In: British Journal of Cancer. Band 111, Nummer 3, Juli 2014, S. 598–602, doi:10.1038/bjc.2014.309, PMID 24918813, PMC 4119982 (freier Volltext).
  • Caren G. Solomon, Frank A. Sinicrope: Lynch Syndrome–Associated Colorectal Cancer. In: New England Journal of Medicine. 379, 2018, S. 764, doi:10.1056/NEJMcp1714533.
  • Robert J. MacInnis, John L. Hopper, Polly A. Newcomb, Noralane M. Lindor, Yingye Zheng: Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer. In: Cancer Epidemiology and Prevention Biomarkers. Band 26, Nr. 3, 1. März 2017, ISSN 1538-7755, S. 404–412, doi:10.1158/1055-9965.EPI-16-0693, PMID 27799157, PMC 5336409 (freier Volltext) – (aacrjournals.org [abgerufen am 30. Dezember 2018]).
  • Verena Steinke, Christoph Engel, Reinhard Büttner, Hans Konrad Schackert, Wolff H Schmiegel: Hereditary Nonpolyposis Colorectal Cancer (HNPCC)/Lynch Syndrome. In: Deutsches Ärzteblatt International. Band 110, Nr. 3, Januar 2013, ISSN 1866-0452, S. 32–38, doi:10.3238/arztebl.2013.0032, PMID 23413378, PMC 3566622 (freier Volltext).
  • D. Ingham, C. P. Diggle, I. Berry, C. A. Bristow, B. E. Hayward, N. Rahman, A. F. Markham, E. G. Sheridan, D. T. Bonthron, I. M. Carr: Simple detection of germline microsatellite instability for diagnosis of constitutional mismatch repair cancer syndrome. In: Human Mutation. Band 34, Nummer 6, Juni 2013, S. 847–852, doi:10.1002/humu.22311, PMID 23483711.

hnpcc.de

mgz-muenchen.de

nejm.org

  • John D. Burn et al.: Effect of Aspirin or Resistant Starch on Colorectal Neoplasia in the Lynch Syndrome. New England Journal of Medicine 359 (11. Dezembver 2008), S. 2567–2578 [1]

nih.gov

ncbi.nlm.nih.gov

  • S. Shiovitz, W. K. Copeland, M. N. Passarelli, A. N. Burnett-Hartman, W. M. Grady, J. D. Potter, S. Gallinger, D. D. Buchanan, C. Rosty, A. K. Win, M. Jenkins, S. N. Thibodeau, R. Haile, J. A. Baron, L. L. Marchand, P. A. Newcomb, N. M. Lindor: Characterisation of familial colorectal cancer Type X, Lynch syndrome, and non-familial colorectal cancer. In: British Journal of Cancer. Band 111, Nummer 3, Juli 2014, S. 598–602, doi:10.1038/bjc.2014.309, PMID 24918813, PMC 4119982 (freier Volltext).
  • Robert J. MacInnis, John L. Hopper, Polly A. Newcomb, Noralane M. Lindor, Yingye Zheng: Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer. In: Cancer Epidemiology and Prevention Biomarkers. Band 26, Nr. 3, 1. März 2017, ISSN 1538-7755, S. 404–412, doi:10.1158/1055-9965.EPI-16-0693, PMID 27799157, PMC 5336409 (freier Volltext) – (aacrjournals.org [abgerufen am 30. Dezember 2018]).
  • Verena Steinke, Christoph Engel, Reinhard Büttner, Hans Konrad Schackert, Wolff H Schmiegel: Hereditary Nonpolyposis Colorectal Cancer (HNPCC)/Lynch Syndrome. In: Deutsches Ärzteblatt International. Band 110, Nr. 3, Januar 2013, ISSN 1866-0452, S. 32–38, doi:10.3238/arztebl.2013.0032, PMID 23413378, PMC 3566622 (freier Volltext).
  • D. Ingham, C. P. Diggle, I. Berry, C. A. Bristow, B. E. Hayward, N. Rahman, A. F. Markham, E. G. Sheridan, D. T. Bonthron, I. M. Carr: Simple detection of germline microsatellite instability for diagnosis of constitutional mismatch repair cancer syndrome. In: Human Mutation. Band 34, Nummer 6, Juni 2013, S. 847–852, doi:10.1002/humu.22311, PMID 23483711.

omim.org

web.archive.org

  • W. Schmiegel u. a.: S3-Leitlinie "Kolorektales Karzinom". In: Zeitschrift für Gastroenterologie. 2008, 46, S. 1–73 (Archivlink (Memento vom 29. Dezember 2009 im Internet Archive))

zdb-katalog.de

  • Robert J. MacInnis, John L. Hopper, Polly A. Newcomb, Noralane M. Lindor, Yingye Zheng: Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer. In: Cancer Epidemiology and Prevention Biomarkers. Band 26, Nr. 3, 1. März 2017, ISSN 1538-7755, S. 404–412, doi:10.1158/1055-9965.EPI-16-0693, PMID 27799157, PMC 5336409 (freier Volltext) – (aacrjournals.org [abgerufen am 30. Dezember 2018]).
  • Verena Steinke, Christoph Engel, Reinhard Büttner, Hans Konrad Schackert, Wolff H Schmiegel: Hereditary Nonpolyposis Colorectal Cancer (HNPCC)/Lynch Syndrome. In: Deutsches Ärzteblatt International. Band 110, Nr. 3, Januar 2013, ISSN 1866-0452, S. 32–38, doi:10.3238/arztebl.2013.0032, PMID 23413378, PMC 3566622 (freier Volltext).