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R Sampson

Showing results (491-500 of 518) with videos related to

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The British Journal of Surgery|May 9, 2024
Updated European guidelines for clinical management of familial adenomatous polyposis (FAP), MUTYH-associated polyposis (MAP), gastric adenocarcinoma, proximal polyposis of the stomach (GAPPS) and other rare adenomatous polyposis syndromes: a joint EHTG-ESCP revisionGloria Zaffaroni, Alessandro Mannucci, Laura Koskenvuo, et al.
Acta Neuropathologica Communications|June 2, 2016
Germline or somatic GPR101 duplication leads to X-linked acrogigantism: a clinico-pathological and genetic studyDonato Iacovazzo, Richard Caswell, Benjamin Bunce, et al.
Familial Cancer|September 19, 2009
Recommendations to improve identification of hereditary and familial colorectal cancer in EuropeH F A Vasen, G Möslein, A Alonso, et al.
Gut|December 15, 2015
Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome databasePål Møller, Toni Seppälä, Inge Bernstein, et al.
Gut|June 5, 2016
Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome databasePål Møller, Toni Seppälä, Inge Bernstein, et al.
Gastroenterology|November 1, 2020
Duodenal Adenomas and Cancer in MUTYH-associated Polyposis: An International Cohort Study, Laura E Thomas, Joanna J Hurley, et al.
Human Mutation|August 21, 2010
Leiden Open Variation Database of the MUTYH geneAstrid A Out, Carli M J Tops, Maartje Nielsen, et al.
Gut|February 15, 2013
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European expertsHans F A Vasen, Ignacio Blanco, Katja Aktan-Collan, et al.
Hereditary Cancer in Clinical Practice|October 20, 2017
Colorectal cancer incidence in <i>path_MLH1</i> carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database reportToni Seppälä, Kirsi Pylvänäinen, Dafydd Gareth Evans, et al.
Science (New York, N.Y.)|August 8, 1997
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34M van Slegtenhorst, R de Hoogt, C Hermans, et al.
Pageof 52

Showing results (491-500 of 518) with videos related to

Sort By:
Pageof 52
The British Journal of Surgery|May 9, 2024
Updated European guidelines for clinical management of familial adenomatous polyposis (FAP), MUTYH-associated polyposis (MAP), gastric adenocarcinoma, proximal polyposis of the stomach (GAPPS) and other rare adenomatous polyposis syndromes: a joint EHTG-ESCP revisionGloria Zaffaroni, Alessandro Mannucci, Laura Koskenvuo, et al.
Acta Neuropathologica Communications|June 2, 2016
Germline or somatic GPR101 duplication leads to X-linked acrogigantism: a clinico-pathological and genetic studyDonato Iacovazzo, Richard Caswell, Benjamin Bunce, et al.
Familial Cancer|September 19, 2009
Recommendations to improve identification of hereditary and familial colorectal cancer in EuropeH F A Vasen, G Möslein, A Alonso, et al.
Gut|December 15, 2015
Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome databasePål Møller, Toni Seppälä, Inge Bernstein, et al.
Gut|June 5, 2016
Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome databasePål Møller, Toni Seppälä, Inge Bernstein, et al.
Gastroenterology|November 1, 2020
Duodenal Adenomas and Cancer in MUTYH-associated Polyposis: An International Cohort Study, Laura E Thomas, Joanna J Hurley, et al.
Human Mutation|August 21, 2010
Leiden Open Variation Database of the MUTYH geneAstrid A Out, Carli M J Tops, Maartje Nielsen, et al.
Gut|February 15, 2013
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European expertsHans F A Vasen, Ignacio Blanco, Katja Aktan-Collan, et al.
Hereditary Cancer in Clinical Practice|October 20, 2017
Colorectal cancer incidence in <i>path_MLH1</i> carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database reportToni Seppälä, Kirsi Pylvänäinen, Dafydd Gareth Evans, et al.
Science (New York, N.Y.)|August 8, 1997
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34M van Slegtenhorst, R de Hoogt, C Hermans, et al.
Pageof 52