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

Year Number of Results
1987 3
1988 8
1989 9
1990 23
1991 23
1992 55
1993 58
1994 61
1995 63
1996 82
1997 76
1998 77
1999 101
2000 76
2001 85
2002 96
2003 63
2004 88
2005 81
2006 97
2007 91
2008 105
2009 83
2010 98
2011 97
2012 83
2013 89
2014 109
2015 105
2016 106
2017 101
2018 96
2019 103
2020 118
2021 109
2022 127
2023 110
2024 40

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2,758 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 …
CONTEXT.-: Familial adenomatous polyposis (FAP) is a rare genetic disorder with autosomal dominant inheritance, …
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. ...Some lesions (skull and mandible osteomas, dental abnormalities, and fibromas on …
Familial adenomatous polyposis (FAP) is characterized by the development of many tens to thousands of adenomas i …
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. ...No consensus is reached on the right type and timing of colectomy. As patients w …
Familial adenomatous polyposis (FAP) and MUTYH-associated polyposis (MAP) are rare inherited polyposis …
Genomic and transcriptomic profiling of carcinogenesis in patients with familial adenomatous polyposis.
Li J, Wang R, Zhou X, Wang W, Gao S, Mao Y, Wu X, Guo L, Liu H, Wen L, Fu W, Tang F. Li J, et al. Gut. 2020 Jul;69(7):1283-1293. doi: 10.1136/gutjnl-2019-319438. Epub 2019 Nov 19. Gut. 2020. PMID: 31744909 Free PMC article.
OBJECTIVE: Familial adenomatous polyposis (FAP) is characterised by the development of hundreds to thousands of adenomas at different evolutionary stages in the colon and rectum that will inevitably progress to adenocarcinomas if left untreated. ...CON …
OBJECTIVE: Familial adenomatous polyposis (FAP) is characterised by the development of hundreds to thousands of …
The genetics of familial adenomatous polyposis (FAP) and MutYH-associated polyposis (MAP).
Claes K, Dahan K, Tejpar S, De Paepe A, Bonduelle M, Abramowicz M, Verellen C, Franchimont D, Van Cutsem E, Kartheuser A. Claes K, et al. Acta Gastroenterol Belg. 2011 Sep;74(3):421-6. Acta Gastroenterol Belg. 2011. PMID: 22103048 Free article. Review.
FAP is characterized by 100-1000s of adenomatous polyps in colon and rectum, and is in 70% of the patients associated with extracolonic manifestations. ...(A)FAP is caused by autosomal dominantly inherited mutations in the APC (Adenomatous polyposis …
FAP is characterized by 100-1000s of adenomatous polyps in colon and rectum, and is in 70% of the patients associated with ext …
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. ...Multiple colorectal adenomas can also be c …
Familial adenomatous polyposis (FAP) is an autosomal-dominant colorectal cancer syndrome, caused by a germline m …
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 los …
Familial adenomatous polyposis (FAP) is a genetic syndrome characterized by the presence of multiple polyps in t …
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.
Patients with FAP are guaranteed to have one major abdominal surgery in their life. ...A successful voyage calls for clinical cooperation between providers and patients, education and understanding, and expertise and experience. FAP patients and families should be i …
Patients with FAP are guaranteed to have one major abdominal surgery in their life. ...A successful voyage calls for clinical coopera …
Familial adenomatous polyposis.
Macrae F, du Sart D, Nasioulas S. Macrae F, et al. Best Pract Res Clin Gastroenterol. 2009;23(2):197-207. doi: 10.1016/j.bpg.2009.02.010. Best Pract Res Clin Gastroenterol. 2009. PMID: 19414146 Free article. Review.
A multimodal approach of complementary techniques targeting primarily truncating, deletion and rearrangement mutations provides a robust screening protocol that identifies the vast majority of pathogenic germline APC gene mutations in FAP patients. Patients in whom no muta …
A multimodal approach of complementary techniques targeting primarily truncating, deletion and rearrangement mutations provides a robust scr …
Familial adenomatous polyposis (FAP) and hereditary nonpolyposis colorectal cancer (HNPCC): a review of clinical, genetic and therapeutic aspects.
Soravia C, Bapat B, Cohen Z. Soravia C, et al. Schweiz Med Wochenschr. 1997 Apr 19;127(16):682-90. Schweiz Med Wochenschr. 1997. PMID: 9140167 Review.
Familial adenomatous polyposis (FAP) and hereditary nonpolyposis colorectal cancer (HNPCC) are two syndromes of colorectal cancer predisposition, inherited in an autosomal dominant fashion. They account for about 1% and 5-7% of all colorectal cancer ca …
Familial adenomatous polyposis (FAP) and hereditary nonpolyposis colorectal cancer (HNPCC) are two syndromes of …
2,758 results