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

Year Number of Results
1979 1
1980 4
1981 1
1982 2
1983 2
1985 1
1986 3
1987 13
1988 21
1989 27
1990 20
1991 28
1992 30
1993 35
1994 58
1995 53
1996 62
1997 52
1998 48
1999 71
2000 70
2001 51
2002 61
2003 52
2004 60
2005 69
2006 49
2007 64
2008 57
2009 49
2010 37
2011 45
2012 41
2013 53
2014 36
2015 39
2016 38
2017 42
2018 27
2019 29
2020 34
2021 28
2022 41
2023 35
2024 3

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1,560 results

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Page 1
Familial Adenomatous Polyposis Syndrome: An Update and Review of Extraintestinal Manifestations.
Dinarvand P, Davaro EP, Doan JV, Ising ME, Evans NR, Phillips NJ, Lai J, Guzman MA. Dinarvand P, et al. Arch Pathol Lab Med. 2019 Nov;143(11):1382-1398. doi: 10.5858/arpa.2018-0570-RA. Epub 2019 May 9. Arch Pathol Lab Med. 2019. PMID: 31070935 Free article. Review.
CONTEXT.-: Familial adenomatous polyposis (FAP) is a rare genetic disorder with autosomal dominant inheritance, defined by numerous adenomatous polyps, which inevitably progress to colorectal carcinoma unless detected and managed early. ...These manifestation …
CONTEXT.-: Familial adenomatous polyposis (FAP) is a rare genetic disorder with autosomal dominant inheritance, defined by num …
Management of familial adenomatous polyposis and MUTYH-associated polyposis; new insights.
Aelvoet AS, Buttitta F, Ricciardiello L, Dekker E. Aelvoet AS, et al. Best Pract Res Clin Gastroenterol. 2022 Jun-Aug;58-59:101793. doi: 10.1016/j.bpg.2022.101793. Epub 2022 Mar 16. Best Pract Res Clin Gastroenterol. 2022. PMID: 35988966 Free article. Review.
Familial adenomatous polyposis (FAP) and MUTYH-associated polyposis (MAP) are rare inherited polyposis syndromes with a high colorectal cancer (CRC) risk. ...Whereas up until recently upper gastrointestinal surveillance was mostly diagnostic and patien …
Familial adenomatous polyposis (FAP) and MUTYH-associated polyposis (MAP) are rare inherited polyposis syndromes …
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.
Familial adenomatous polyposis (FAP) is characterized by the development of many tens to thousands of adenomas in the rectum and colon during the second decade of life. ...Classic FAP is inherited in an autosomal dominant manner and results from a germline mutation …
Familial adenomatous polyposis (FAP) is characterized by the development of many tens to thousands of adenomas in the rectum a …
Familial and hereditary gastric cancer, an overview.
Carneiro F. Carneiro F. Best Pract Res Clin Gastroenterol. 2022 Jun-Aug;58-59:101800. doi: 10.1016/j.bpg.2022.101800. Epub 2022 May 4. Best Pract Res Clin Gastroenterol. 2022. PMID: 35988963 Review.
There are three major hereditable syndromes that affect primarily the stomach: hereditary diffuse gastric cancer (HDGC), gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS) and familial intestinal gastric cancer (FIGC). ...Gastric cancer can also be observ …
There are three major hereditable syndromes that affect primarily the stomach: hereditary diffuse gastric cancer (HDGC), gastric adenocarcin …
Evolving strategies for management of desmoid tumor.
Riedel RF, Agulnik M. Riedel RF, et al. Cancer. 2022 Aug 15;128(16):3027-3040. doi: 10.1002/cncr.34332. Epub 2022 Jun 7. Cancer. 2022. PMID: 35670122 Free PMC article. Review.
Most DTs are sporadic, harboring somatic mutations in the gene that encodes for beta-catenin, whereas DTs occurring in patients with familial adenomatous polyposis have germline mutations in the APC gene, which encodes for a protein regulator of beta-catenin. ...
Most DTs are sporadic, harboring somatic mutations in the gene that encodes for beta-catenin, whereas DTs occurring in patients with familia …
Molecular genetics of colorectal cancer.
Fearon ER. Fearon ER. Annu Rev Pathol. 2011;6:479-507. doi: 10.1146/annurev-pathol-011110-130235. Annu Rev Pathol. 2011. PMID: 21090969 Review.
[Gastrointestinal polyposis syndromes].
Spier I, Hüneburg R, Aretz S. Spier I, et al. Internist (Berl). 2021 Feb;62(2):133-144. doi: 10.1007/s00108-020-00903-z. Internist (Berl). 2021. PMID: 33237439 Review. German.
MATERIALS AND METHODS: The present article is based on a literature search on gastrointestinal polyposis syndromes. RESULTS: In addition to familial adenomatous polyposis (FAP), there are further subtypes of adenomatous polyposis that can often …
MATERIALS AND METHODS: The present article is based on a literature search on gastrointestinal polyposis syndromes. RESULTS: In addit …
Oral manifestations in patients with familial adenomatous polyposis: A systematic review and meta-analysis.
Almeida FT, Pachêco-Pereira C, Porporatti AL, Flores-Mir C, Leite AF, De Luca Canto G, Guerra EN. Almeida FT, et al. J Gastroenterol Hepatol. 2016 Mar;31(3):527-40. doi: 10.1111/jgh.13149. J Gastroenterol Hepatol. 2016. PMID: 26331960 Review.
BACKGROUND AND AIM: The oral manifestations of familial adenomatous polyposis (FAP) have been reported in the recent literature. ...
BACKGROUND AND AIM: The oral manifestations of familial adenomatous polyposis (FAP) have been reported in the recent literatur …
Desmoid Tumors in Familial Adenomatous Polyposis.
DE Marchis ML, Tonelli F, Quaresmini D, Lovero D, Della-Morte D, Silvestris F, Guadagni F, Palmirotta R. DE Marchis ML, et al. Anticancer Res. 2017 Jul;37(7):3357-3366. doi: 10.21873/anticanres.11702. Anticancer Res. 2017. PMID: 28668823 Review.
Familial adenomatous polyposis (FAP) is a cancer syndrome caused by a germline mutation in the adenomatous polyposis coli (APC) gene. ...
Familial adenomatous polyposis (FAP) is a cancer syndrome caused by a germline mutation in the adenomatous polyposis
Familial adenomatous polyposis.
Church J. Church J. Surg Oncol Clin N Am. 2009 Oct;18(4):585-98. doi: 10.1016/j.soc.2009.07.002. Surg Oncol Clin N Am. 2009. PMID: 19793567 Free article. Review.
1,560 results