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

Year Number of Results
1975 1
1979 1
1981 1
1983 2
1987 3
1988 2
1989 4
1990 2
1991 4
1992 3
1993 10
1994 8
1995 15
1996 16
1997 11
1998 15
1999 23
2000 25
2001 22
2002 33
2003 36
2004 31
2005 28
2006 20
2007 28
2008 18
2009 15
2010 18
2011 14
2012 23
2013 32
2014 18
2015 17
2016 23
2017 20
2018 14
2019 7
2020 11
2021 9
2022 12
2023 11
2024 2

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565 results

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Page 1
Hereditary and familial colon cancer.
Jasperson KW, Tuohy TM, Neklason DW, Burt RW. Jasperson KW, et al. Gastroenterology. 2010 Jun;138(6):2044-58. doi: 10.1053/j.gastro.2010.01.054. Gastroenterology. 2010. PMID: 20420945 Free PMC article. Review.
Between 2% to 5% of all colon cancers arise in the setting of well-defined inherited syndromes, including Lynch syndrome, familial adenomatous polyposis, MUTYH-associated polyposis, and certain hamartomatous polyposis conditions. ...This …
Between 2% to 5% of all colon cancers arise in the setting of well-defined inherited syndromes, including Lynch syndrome, familial …
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.
Colorectal cancer (CRC) accounts for over 8% of all deaths annually worldwide. Between 2 and 5% of all CRCs occur due to inherited syndromes, including Lynch syndrome, familial adenomatous polyposis, MUTYH-associated polyposis, Peutz-Jeghers syn …
Colorectal cancer (CRC) accounts for over 8% of all deaths annually worldwide. Between 2 and 5% of all CRCs occur due to inherited sy …
Main genetic entities associated with supernumerary teeth.
Cammarata-Scalisi F, Avendaño A, Callea M. Cammarata-Scalisi F, et al. Arch Argent Pediatr. 2018 Dec 1;116(6):437-444. doi: 10.5546/aap.2018.eng.437. Arch Argent Pediatr. 2018. PMID: 30457727 Free article. Review. English, Spanish.
Supernumerary teeth represent a common human dental anomaly, defined as presence of extra teeth-more than the normal number foreseen in primary or permanent dentition. The prevalence has been reported between 0.2 to 3%, and is more frequent in males than females. The etiol …
Supernumerary teeth represent a common human dental anomaly, defined as presence of extra teeth-more than the normal number foreseen in prim …
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.
The initial assessment is the collection of a family history of cancers and premalignant gastrointestinal conditions and should provide enough information to develop a preliminary determination of the risk of a familial predisposition to cancer. Age at diagnosis and lineag …
The initial assessment is the collection of a family history of cancers and premalignant gastrointestinal conditions and should provide enou …
MutYH-associated polyposis.
Toboeva MK, Shelygin YA, Frolov SA, Kuzminov MA, Tsukanov AS. Toboeva MK, et al. Ter Arkh. 2019 Mar 18;91(2):97-100. doi: 10.26442/00403660.2019.02.000124. Ter Arkh. 2019. PMID: 31094179 Review.
MutYH-associated polyposis is the only polyposis syndrome with an autosomal recessive type of inheritance, often phenotypically similar to a weakened form of familial adenomatous polyposis. For the development of the disease mutations in both al …
MutYH-associated polyposis is the only polyposis syndrome with an autosomal recessive type of inheritance, often phenotypicall …
Aggressive fibromatosis.
Fisher C, Thway K. Fisher C, et al. Pathology. 2014 Feb;46(2):135-40. doi: 10.1097/PAT.0000000000000045. Pathology. 2014. PMID: 24378386 Review.
In sporadic cases there are somatic mutations in the beta-catenin (CTNNB1) gene on 3p21, resulting in immunohistochemically demonstrable overexpression in nuclei. Fibromatosis in patients with familial adenomatous polyposis (FAP) harbours inactivating germlin …
In sporadic cases there are somatic mutations in the beta-catenin (CTNNB1) gene on 3p21, resulting in immunohistochemically demonstrable ove …
Hereditary gastrointestinal cancer.
Hata K, Yamamoto Y, Kiyomatsu T, Tanaka T, Kazama S, Nozawa H, Kawai K, Tanaka J, Nishikawa T, Otani K, Yasuda K, Kishikawa J, Nagai Y, Anzai H, Shinagawa T, Arakawa K, Yamaguchi H, Ishihara S, Sunami E, Kitayama J, Watanabe T. Hata K, et al. Surg Today. 2016 Oct;46(10):1115-22. doi: 10.1007/s00595-015-1283-3. Epub 2015 Dec 16. Surg Today. 2016. PMID: 26676416 Review.
A substantial proportion of patients with GI cancer have a familial history, and several causative genes have been identified. ...In this review, we provide an overview and discuss the diagnosis, genetic testing, and management of four major hereditary GI cancers: famil …
A substantial proportion of patients with GI cancer have a familial history, and several causative genes have been identified. ...In …
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 …
Familial adenomatous polyposis (FAP) is an autosomal-dominant colorectal cancer syndrome, caused by a germline mutation …
MUTYH-associated polyposis.
Sampson JR, Jones N. Sampson JR, et al. Best Pract Res Clin Gastroenterol. 2009;23(2):209-18. doi: 10.1016/j.bpg.2009.03.006. Best Pract Res Clin Gastroenterol. 2009. PMID: 19414147 Review.
MUTYH-associated polyposis (MAP) is an autosomal recessive disorder characterised by adenomatous polyps of the colorectum and a very high risk of colorectal cancer. It appears to be at least as prevalent as autosomal dominant familial adenomatous po …
MUTYH-associated polyposis (MAP) is an autosomal recessive disorder characterised by adenomatous polyps of the colorectum and …
565 results