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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 5

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1,562 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 …
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 …
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 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.
Molecular Pathways of Carcinogenesis in Familial Adenomatous Polyposis.
Ditonno I, Novielli D, Celiberto F, Rizzi S, Rendina M, Ierardi E, Di Leo A, Losurdo G. Ditonno I, et al. Int J Mol Sci. 2023 Mar 16;24(6):5687. doi: 10.3390/ijms24065687. Int J Mol Sci. 2023. PMID: 36982759 Free PMC article. Review.
Familial adenomatous polyposis (FAP) is a genetic syndrome characterized by the presence of multiple polyps in the gastrointestinal tract and a wide range of systemic extra-intestinal manifestations. ...The pathogenesis of the disease is based on a loss of function …
Familial adenomatous polyposis (FAP) is a genetic syndrome characterized by the presence of multiple polyps in the gastrointes …
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.
Familial adenomatous polyposis.
Galiatsatos P, Foulkes WD. Galiatsatos P, et al. Am J Gastroenterol. 2006 Feb;101(2):385-98. doi: 10.1111/j.1572-0241.2006.00375.x. Am J Gastroenterol. 2006. PMID: 16454848 Review.
Familial adenomatous polyposis (FAP) is an autosomal-dominant colorectal cancer syndrome, caused by a germline mutation in the adenomatous polyposis coli (APC) gene, on chromosome 5q21. It is characterized by hundreds of adenomatous color …
Familial adenomatous polyposis (FAP) is an autosomal-dominant colorectal cancer syndrome, caused by a germline mutation in the …
Hereditary colorectal, gastric, and pancreatic cancer: comprehensive review.
Seppälä TT, Burkhart RA, Katona BW. Seppälä TT, et al. BJS Open. 2023 May 5;7(3):zrad023. doi: 10.1093/bjsopen/zrad023. BJS Open. 2023. PMID: 37165697 Free PMC article. Review.
METHODS: A narrative review based on recent relevant literature was conducted. RESULTS: Lynch syndrome, formerly known as hereditary non-polyposis colorectal cancer, increases the risk of several abdominal cancers, with the highest population prevalence. Familial adenom …
METHODS: A narrative review based on recent relevant literature was conducted. RESULTS: Lynch syndrome, formerly known as hereditary non- …
1,562 results