Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1966 1
1974 1
1975 1
1978 2
1984 1
1986 1
1987 3
1988 1
1989 2
1990 1
1991 1
1992 1
1993 1
1994 5
1995 6
1996 4
1997 4
1998 2
1999 10
2000 8
2001 6
2002 2
2003 4
2004 6
2005 8
2006 6
2007 6
2008 6
2009 5
2010 7
2011 10
2012 7
2013 5
2014 6
2015 9
2016 9
2017 11
2018 3
2019 7
2020 8
2021 7
2022 8
2023 5
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

196 results

Results by year

Filters applied: . Clear all
Page 1
Hereditary Colorectal Cancer.
Hampel H, Kalady MF, Pearlman R, Stanich PP. Hampel H, et al. Hematol Oncol Clin North Am. 2022 Jun;36(3):429-447. doi: 10.1016/j.hoc.2022.02.002. Epub 2022 May 13. Hematol Oncol Clin North Am. 2022. PMID: 35577708 Review.
The hereditary colorectal cancer syndromes can be divided into two major categories, the nonpolyposis and the polyposis conditions. The nonpolyposis conditions can be divided into those that lead to colorectal tumors with defective mismatch repair and those that do not. Th …
The hereditary colorectal cancer syndromes can be divided into two major categories, the nonpolyposis and the polyposis conditions. T …
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. ...
Between 2% to 5% of all colon cancers arise in the setting of well-defined inherited syndromes, including Lynch syndrome, familial adenomato …
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.
This guideline specifically discusses genetic testing and management of Lynch syndrome, familial adenomatous polyposis (FAP), attenuated familial adenomatous polyposis (AFAP), MUTYH-associated polyposis (MAP), Peutz-Jeghers syndrome, juvenile polyposis
This guideline specifically discusses genetic testing and management of Lynch syndrome, familial adenomatous polyposis (FAP), attenua …
Peutz-Jeghers syndrome.
Tacheci I, Kopacova M, Bures J. Tacheci I, et al. Curr Opin Gastroenterol. 2021 May 1;37(3):245-254. doi: 10.1097/MOG.0000000000000718. Curr Opin Gastroenterol. 2021. PMID: 33591027 Review.
PURPOSE OF REVIEW: Peutz-Jeghers syndrome is a rare, autosomal dominant, hereditary polyposis syndrome defined by gastrointestinal hamartomas and mucocutaneous pigmentations, caused by a germline mutation in the serine/ threonine kinase 11 or liver kinase B1 (STK11/LKB1) g …
PURPOSE OF REVIEW: Peutz-Jeghers syndrome is a rare, autosomal dominant, hereditary polyposis syndrome defined by gastrointestinal ha …
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 …
Between 2 and 5% of all CRCs occur due to inherited syndromes, including Lynch syndrome, familial adenomatous polyposis, MUTYH-associ …
Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Familial Tumor Syndromes.
Nosé V, Lazar AJ. Nosé V, et al. Head Neck Pathol. 2022 Mar;16(1):143-157. doi: 10.1007/s12105-022-01414-z. Epub 2022 Mar 21. Head Neck Pathol. 2022. PMID: 35312981 Free PMC article. Review.
This review highlights the important findings within these syndromes, especially on the update on syndromes with tumors involving the head and neck region, as Gorlin syndrome/nevoid basal cell carcinoma syndrome associated with odontogenic keratocysts; Brooke-Spiegler syndrome/fa …
This review highlights the important findings within these syndromes, especially on the update on syndromes with tumors involving the head a …
Clinical Guidelines for Diagnosis and Management of Peutz-Jeghers Syndrome in Children and Adults.
Yamamoto H, Sakamoto H, Kumagai H, Abe T, Ishiguro S, Uchida K, Kawasaki Y, Saida Y, Sano Y, Takeuchi Y, Tajika M, Nakajima T, Banno K, Funasaka Y, Hori S, Yamaguchi T, Yoshida T, Ishikawa H, Iwama T, Okazaki Y, Saito Y, Matsuura N, Mutoh M, Tomita N, Akiyama T, Yamamoto T, Ishida H, Nakayama Y. Yamamoto H, et al. Digestion. 2023;104(5):335-347. doi: 10.1159/000529799. Epub 2023 Apr 13. Digestion. 2023. PMID: 37054692 Free article. Review.
BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare disease characterized by the presence of hamartomatous polyposis throughout the gastrointestinal tract, except for the esophagus, along with characteristic mucocutaneous pigmentation. ...Some patients with PJS devel …
BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare disease characterized by the presence of hamartomatous polyposis throughout …
Pathology of Gastrointestinal Polyposis Disorders.
Rosty C, Brosens LAA. Rosty C, et al. Gastroenterol Clin North Am. 2024 Mar;53(1):179-200. doi: 10.1016/j.gtc.2023.09.006. Epub 2023 Oct 20. Gastroenterol Clin North Am. 2024. PMID: 38280747 Review.
Adenomatous polyposis syndromes comprise the prototypical familial adenomatous polyposis syndrome and other recently identified genetic conditions inherited in a dominant or recessive manner. Serrated polyposis syndrome is defined by arbitrary clinical criter …
Adenomatous polyposis syndromes comprise the prototypical familial adenomatous polyposis syndrome and other recently identifie …
[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.
In hamartomatous polyposis syndromes, the clinical overlaps often cause differential diagnostic problems. Serratated polyposis syndrome is possibly the most frequent polyposis syndrome, although its cause is currently largely unexplained. ...
In hamartomatous polyposis syndromes, the clinical overlaps often cause differential diagnostic problems. Serratated polypo
The hamartomatous polyposis syndromes: a clinical and molecular review.
Schreibman IR, Baker M, Amos C, McGarrity TJ. Schreibman IR, et al. Am J Gastroenterol. 2005 Feb;100(2):476-90. doi: 10.1111/j.1572-0241.2005.40237.x. Am J Gastroenterol. 2005. PMID: 15667510 Review.
The hamartomatous polyposis syndromes are characterized by an overgrowth of cells native to the area in which they normally occur. ...Hereditary mixed polyposis syndrome is a variant of juvenile polyposis characterized by both hamartomatous and …
The hamartomatous polyposis syndromes are characterized by an overgrowth of cells native to the area in which they normally oc …
196 results