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

Year Number of Results
1966 2
1968 2
1969 3
1970 2
1971 1
1972 1
1973 2
1974 3
1975 2
1976 6
1977 1
1978 1
1979 3
1980 6
1981 1
1982 3
1983 3
1984 1
1985 2
1986 1
1987 10
1988 15
1989 17
1990 11
1991 20
1992 16
1993 20
1994 24
1995 42
1996 36
1997 40
1998 27
1999 49
2000 50
2001 41
2002 45
2003 40
2004 39
2005 44
2006 44
2007 47
2008 28
2009 37
2010 31
2011 36
2012 33
2013 30
2014 28
2015 28
2016 34
2017 26
2018 12
2019 21
2020 33
2021 18
2022 30
2023 24
2024 4

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Search Results

1,121 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 manifestations have …
CONTEXT.-: Familial adenomatous polyposis (FAP) is a rare genetic disorder with autosomal dominant inheritance, defined by num …
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 rec
Genetic testing should be conducted in the context of pre- and post-test genetic counseling to ensure the patient's informed d
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). ...GAPPS is caused by germlin …
There are three major hereditable syndromes that affect primarily the stomach: hereditary diffuse gastric cancer (HDGC), gastric adenocarcin …
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 patients were …
Familial adenomatous polyposis (FAP) and MUTYH-associated polyposis (MAP) are rare inherited polyposis syndromes with a …
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.
Over the past three decades, molecular genetic studies have revealed some critical mutations underlying the pathogenesis of the sporadic and inherited forms of colorectal cancer (CRC). ...Much work remains to be done to fully understand the nature and significance of the i …
Over the past three decades, molecular genetic studies have revealed some critical mutations underlying the pathogenesis of the spora …
Pathology and genetics of hereditary colorectal cancer.
Ma H, Brosens LAA, Offerhaus GJA, Giardiello FM, de Leng WWJ, Montgomery EA. Ma H, et al. Pathology. 2018 Jan;50(1):49-59. doi: 10.1016/j.pathol.2017.09.004. Epub 2017 Nov 21. Pathology. 2018. PMID: 29169633 Review.
Between 2 and 5% of all CRCs occur due to inherited syndromes, including Lynch syndrome, familial adenomatous polyposis, MUTYH-associated polyposis, Peutz-Jeghers syndrome, juvenile polyposis and Cowden/PTEN hamartoma syndrome. In addition, serrated polypo
Between 2 and 5% of all CRCs occur due to inherited syndromes, including Lynch syndrome, familial adenomatous polyposis, MUTYH-associ …
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 …
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.
Whenever possible, the clinical diagnosis should be confirmed by genetic testing. When the APC mutation in the family has been identified, genetic testing of all first-degree relatives should be performed. Presymptomatic and prenatal (amniocentesis and chorionic vil …
Whenever possible, the clinical diagnosis should be confirmed by genetic testing. When the APC mutation in the family has been identi …
Peutz-Jeghers syndrome: a systematic review and recommendations for management.
Beggs AD, Latchford AR, Vasen HF, Moslein G, Alonso A, Aretz S, Bertario L, Blanco I, Bülow S, Burn J, Capella G, Colas C, Friedl W, Møller P, Hes FJ, Järvinen H, Mecklin JP, Nagengast FM, Parc Y, Phillips RK, Hyer W, Ponz de Leon M, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Tejpar S, Thomas HJ, Wijnen JT, Clark SK, Hodgson SV. Beggs AD, et al. Gut. 2010 Jul;59(7):975-86. doi: 10.1136/gut.2009.198499. Gut. 2010. PMID: 20581245
The proposed guidelines contained in this article have been produced as a consensus statement on behalf of a group of European experts who met in Mallorca in 2007 and who have produced guidelines on the clinical management of Lynch syndrome and familial adenomatous polyposis
The proposed guidelines contained in this article have been produced as a consensus statement on behalf of a group of European experts who m …
Cancer Genetics.
Van Cott C. Van Cott C. Surg Clin North Am. 2020 Jun;100(3):483-498. doi: 10.1016/j.suc.2020.02.012. Epub 2020 Apr 16. Surg Clin North Am. 2020. PMID: 32402295 Review.
Genetic testing provides a tool to determine those patients with a genetic mutation and to whom appropriate preventive care and treatment may be offered. It is imperative for general surgeons to understand the role genetics plays in the care of individual pat
Genetic testing provides a tool to determine those patients with a genetic mutation and to whom appropriate preventive care an
1,121 results