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2025

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2008 2
2009 2
2010 1
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Page 1
Hereditary Colorectal Cancer.
Hampel H, Kalady MF, Pearlman R, Stanich PP. Hampel H, et al. Hematol Oncol Clin North Am. 2022 Jun;36(3):429-447. doi: 10.1016/j.hoc.2022.02.002. Epub 2022 May 13. Hematol Oncol Clin North Am. 2022. PMID: 35577708 Review.
Some of these variants are in cancer genes that are associated with colorectal cancer while others are not. The hereditary colorectal cancer syndromes can be divided into two major categories, the nonpolyposis and the polyposis conditions. The nonpolyposis co …
Some of these variants are in cancer genes that are associated with colorectal cancer while others are not. The hereditary colorectal …
Familial adenomatous polyposis.
Half E, Bercovich D, Rozen P. Half E, et al. Orphanet J Rare Dis. 2009 Oct 12;4:22. doi: 10.1186/1750-1172-4-22. Orphanet J Rare Dis. 2009. PMID: 19822006 Free PMC article. Review.
In a subset of individuals, a MUTYH mutation causes a recessively inherited polyposis condition, MUTYH-associated polyposis (MAP), which is characterized by a slightly increased risk of developing CRC and polyps/adenomas in both the upper and lower gastrointestinal …
In a subset of individuals, a MUTYH mutation causes a recessively inherited polyposis condition, MUTYH-associated polyposis (M …
Update on genetic predisposition to colorectal cancer and polyposis.
Valle L, de Voer RM, Goldberg Y, Sjursen W, Försti A, Ruiz-Ponte C, Caldés T, Garré P, Olsen MF, Nordling M, Castellvi-Bel S, Hemminki K. Valle L, et al. Mol Aspects Med. 2019 Oct;69:10-26. doi: 10.1016/j.mam.2019.03.001. Epub 2019 Mar 18. Mol Aspects Med. 2019. PMID: 30862463 Free article. Review.
The present article summarizes recent developments in the characterization of genetic predisposition to colorectal cancer (CRC). The main themes covered include new hereditary CRC and polyposis syndromes, non-CRC hereditary cancer genes found mutated i …
The present article summarizes recent developments in the characterization of genetic predisposition to colorectal cancer (CRC). The main th …
Hamartomatous polyposis syndromes.
Calva D, Howe JR. Calva D, et al. Surg Clin North Am. 2008 Aug;88(4):779-817, vii. doi: 10.1016/j.suc.2008.05.002. Surg Clin North Am. 2008. PMID: 18672141 Free PMC article. Review.
These syndromes include juvenile polyposis, Peutz-Jeghers syndrome, hereditary mixed polyposis syndrome, and the phosphatase and tensin homolog gene (PTEN) hamartoma tumor syndromes (Cowden and Bannayan-Riley-Ruvalcaba sy
These syndromes include juvenile polyposis, Peutz-Jeghers syndrome, hereditary mixed polyposis
Hamartomatous polyposis syndrome associated malignancies: Risk, pathogenesis and endoscopic surveillance.
Liu S, Ma Y, You W, Li J, Li JN, Qian JM. Liu S, et al. J Dig Dis. 2021 Aug;22(8):444-451. doi: 10.1111/1751-2980.13029. Epub 2021 Jul 8. J Dig Dis. 2021. PMID: 34145757 Review.
Hamartomatous polyposis syndromes (HPS) are a heterogeneous spectrum of diseases that are characterized by diffuse hamartomatous polyps lining the gastrointestinal (GI) tract together with extra-GI manifestations. Classical HPS includes juvenile polyposis
Hamartomatous polyposis syndromes (HPS) are a heterogeneous spectrum of diseases that are characterized by diffuse hamartomato …
Genomic landscape of colorectal carcinogenesis.
Kim JC, Bodmer WF. Kim JC, et al. J Cancer Res Clin Oncol. 2022 Mar;148(3):533-545. doi: 10.1007/s00432-021-03888-w. Epub 2022 Jan 20. J Cancer Res Clin Oncol. 2022. PMID: 35048197 Review.
Otherwise, recently verified FCRC can be particularly notable, for example, EPCAM-associated Lynch syndrome, polymerase proofreading-associated polyposis, RNF43-associated polyposis syndrome or NTHL1 tumour syndrome, and hereditary mix
Otherwise, recently verified FCRC can be particularly notable, for example, EPCAM-associated Lynch syndrome, polymerase proofreading- …
Hamartomatous polyposis syndromes: a review.
Jelsig AM, Qvist N, Brusgaard K, Nielsen CB, Hansen TP, Ousager LB. Jelsig AM, et al. Orphanet J Rare Dis. 2014 Jul 15;9:101. doi: 10.1186/1750-1172-9-101. Orphanet J Rare Dis. 2014. PMID: 25022750 Free PMC article. Review.
Hamartomatous Polyposis Syndromes (HPS) are genetic syndromes, which include Peutz-Jeghers syndrome, Juvenile polyposis syndrome, PTEN hamartoma tumour syndrome (Cowden Syndrom, Bannayan-Riley-Ruvalcaba and Proteus Syndro
Hamartomatous Polyposis Syndromes (HPS) are genetic syndromes, which include Peutz-Jeghers syndrome, Juvenile …
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.
BACKGROUND: Hereditary gastrointestinal polyposis syndromes account for about 1% of all cases of colorectal cancer and are associated with a broad spectrum of extracolonic tumors. ...Aside from the monogenic polyposes, there are many other types of polypos
BACKGROUND: Hereditary gastrointestinal polyposis syndromes account for about 1% of all cases of colorectal cancer and …
The hamartomatous polyposis syndromes: a clinical and molecular review.
Schreibman IR, Baker M, Amos C, McGarrity TJ. Schreibman IR, et al. Am J Gastroenterol. 2005 Feb;100(2):476-90. doi: 10.1111/j.1572-0241.2005.40237.x. Am J Gastroenterol. 2005. PMID: 15667510 Review.
Patients afflicted with these syndromes are also at significant risk for extraintestinal malignancies. Seven inherited hamartomatous polyposis syndromes have been described: familial juvenile polyposis syndrome, Cowden's syndrome, Bannaya …
Patients afflicted with these syndromes are also at significant risk for extraintestinal malignancies. Seven inherited hamartomatous …
23 results