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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 1
2005 2
2007 1
2010 1
2011 1
2012 4
2014 1
2015 2
2017 1
2018 1
2019 3
2022 3
2023 4
2024 0

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Page 1
ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
Syngal S, Brand RE, Church JM, Giardiello FM, Hampel HL, Burt RW; American College of Gastroenterology. Syngal S, et al. Am J Gastroenterol. 2015 Feb;110(2):223-62; quiz 263. doi: 10.1038/ajg.2014.435. Epub 2015 Feb 3. Am J Gastroenterol. 2015. PMID: 25645574 Free PMC article. Review.
Genetic testing should be conducted in the context of pre- and post-test genetic counseling to ensure the patient's informed decision making. Patients who meet clinical criteria for a syndrome as well as those with identified pathogenic germline mutations should receive ap …
Genetic testing should be conducted in the context of pre- and post-test genetic counseling to ensure the patient's informed decision making …
Genetic Predisposition to Colorectal Cancer: How Many and Which Genes to Test?
Rebuzzi F, Ulivi P, Tedaldi G. Rebuzzi F, et al. Int J Mol Sci. 2023 Jan 21;24(3):2137. doi: 10.3390/ijms24032137. Int J Mol Sci. 2023. PMID: 36768460 Free PMC article. Review.
Colorectal cancer is one of the most common tumors, and genetic predisposition is one of the key risk factors in the development of this malignancy. Lynch syndrome and familial adenomatous polyposis are the best-known genetic diseases associated with hereditary colo …
Colorectal cancer is one of the most common tumors, and genetic predisposition is one of the key risk factors in the development of this mal …
Hamartomatous polyps: Diagnosis, surveillance, and management.
Gorji L, Albrecht P. Gorji L, et al. World J Gastroenterol. 2023 Feb 28;29(8):1304-1314. doi: 10.3748/wjg.v29.i8.1304. World J Gastroenterol. 2023. PMID: 36925460 Free PMC article. Review.
Hereditary polyposis syndrome can be divided into three categories: Ade-nomatous, serrated, and hamartomatous polyps. ...These syndromes exhibit hamartomatous gastrointestinal polyps in conjunction to extra-intestinal manifestations, which require conscientious and …
Hereditary polyposis syndrome can be divided into three categories: Ade-nomatous, serrated, and hamartomatous polyps. ...These …
Updates in the diagnosis and management of non-ampullary small-bowel polyposis.
Lucaciu L, Yano T, Saurin JC. Lucaciu L, et al. Best Pract Res Clin Gastroenterol. 2023 Jun-Aug;64-65:101852. doi: 10.1016/j.bpg.2023.101852. Epub 2023 Jul 22. Best Pract Res Clin Gastroenterol. 2023. PMID: 37652652 Review.
Advances in endoscopic instruments and techniques changed the strategy of diagnosis and management for non-ampullary small-bowel polyposis. In patients with Peutz-Jeghers syndrome, gastrointestinal surveillance using capsule endoscopy should commence no later than e …
Advances in endoscopic instruments and techniques changed the strategy of diagnosis and management for non-ampullary small-bowel polyposi …
Diagnosis and Management of Cancer Risk in the Gastrointestinal Hamartomatous Polyposis Syndromes: Recommendations From the US Multi-Society Task Force on Colorectal Cancer.
Boland CR, Idos GE, Durno C, Giardiello FM, Anderson JC, Burke CA, Dominitz JA, Gross S, Gupta S, Jacobson BC, Patel SG, Shaukat A, Syngal S, Robertson DJ. Boland CR, et al. Gastroenterology. 2022 Jun;162(7):2063-2085. doi: 10.1053/j.gastro.2022.02.021. Epub 2022 Apr 26. Gastroenterology. 2022. PMID: 35487791
They include Peutz-Jeghers syndrome, juvenile polyposis syndrome, the PTEN hamartoma tumor syndrome (including Cowden's syndrome and Bannayan-Riley-Ruvalcaba syndrome), and hereditary mixed polyposis syndrome. ...Pati …
They include Peutz-Jeghers syndrome, juvenile polyposis syndrome, the PTEN hamartoma tumor syndrome (incl …
The differential diagnosis and surveillance of hereditary gastrointestinal polyposis syndromes.
Aretz S. Aretz S. Dtsch Arztebl Int. 2010 Mar;107(10):163-73. doi: 10.3238/arztebl.2010.0163. Epub 2010 Mar 12. Dtsch Arztebl Int. 2010. PMID: 20358032 Free PMC article. Review.
In recent years, the rate of detection of mutations has risen by 10% to 30%, and clinically relevant genotype-phenotype correlations have been described for juvenile polyposis syndrome. Except in cases of mild adenomatous polyposis, phenotypic overlap …
In recent years, the rate of detection of mutations has risen by 10% to 30%, and clinically relevant genotype-phenotype correlations have be …
Management of small bowel polyps: A literature review.
de Latour RA, Kilaru SM, Gross SA. de Latour RA, et al. Best Pract Res Clin Gastroenterol. 2017 Aug;31(4):401-408. doi: 10.1016/j.bpg.2017.06.003. Epub 2017 Jun 27. Best Pract Res Clin Gastroenterol. 2017. PMID: 28842049 Review.
Benign small bowel lesions include lipomas, lymphangiomas, leiomyomas, neurofibromas, nodular lymphoid hyperplasia and adenomas, many of which are precursors to malignant lesions. Several polyposis syndromes are associated with small bowel polyps as well, including familia …
Benign small bowel lesions include lipomas, lymphangiomas, leiomyomas, neurofibromas, nodular lymphoid hyperplasia and adenomas, many of whi …
Hereditary colorectal cancer: risk assessment and management.
Hampel H, Peltomaki P. Hampel H, et al. Clin Genet. 2000 Aug;58(2):89-97. doi: 10.1034/j.1399-0004.2000.580201.x. Clin Genet. 2000. PMID: 11005140 Review.
There are at least nine major cancer susceptibility syndromes that infer an increased risk for colorectal cancer and/or colorectal polyposis; hereditary nonpolyposis colorectal cancer syndrome, Muir-Torre syndrome, Turcot syndrome, the I1307K polymorph …
There are at least nine major cancer susceptibility syndromes that infer an increased risk for colorectal cancer and/or colorectal polypo …
Hereditary gastrointestinal carcinomas and their precursors: An algorithm for genetic testing.
Spoto CPE, Gullo I, Carneiro F, Montgomery EA, Brosens LAA. Spoto CPE, et al. Semin Diagn Pathol. 2018 May;35(3):170-183. doi: 10.1053/j.semdp.2018.01.004. Epub 2018 Jan 31. Semin Diagn Pathol. 2018. PMID: 29397239 Review.
This review recapitulates the clinical, pathological and molecular aspects of Hereditary Diffuse Gastric Cancer and Gastric Adenocarcinoma and Proximal Polyposis of the Stomach, as well as hereditary colorectal cancer syndromes such as Lynch syndrome and gastrointes …
This review recapitulates the clinical, pathological and molecular aspects of Hereditary Diffuse Gastric Cancer and Gastric Adenocarcinoma a …
Hereditary Gastrointestinal Cancer Syndromes: Role of Imaging in Screening, Diagnosis, and Management.
Katabathina VS, Menias CO, Khanna L, Murphy L, Dasyam AK, Lubner MG, Prasad SR. Katabathina VS, et al. Radiographics. 2019 Sep-Oct;39(5):1280-1301. doi: 10.1148/rg.2019180185. Epub 2019 Aug 2. Radiographics. 2019. PMID: 31373866 Review.
Hereditary gastrointestinal (GI) cancer syndromes due to specific germline mutations are characterized by an increased risk of GI tract malignancies, extra-GI tract cancers, and benign abnormalities. These syndromes include Lynch syndrome, familial adenomatous polyposis …
Hereditary gastrointestinal (GI) cancer syndromes due to specific germline mutations are characterized by an increased risk of GI tract mali …
23 results