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
2004 3
2005 2
2006 5
2007 9
2008 5
2009 2
2010 1
2011 3
2012 1
2013 1
2014 3
2016 1
2018 1
2021 1
2022 1
2023 1
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

37 results

Results by year

Filters applied: . Clear all
Page 1
Lynch syndrome and MYH-associated polyposis: review and testing strategy.
Goodenberger M, Lindor NM. Goodenberger M, et al. J Clin Gastroenterol. 2011 Jul;45(6):488-500. doi: 10.1097/MCG.0b013e318206489c. J Clin Gastroenterol. 2011. PMID: 21325953 Review.
Lynch syndrome caused by defects in DNA mismatch repair genes, and diagnostic testing for Lynch syndrome begins with microsatellite instability and immunohistochemical analysis on the tumor specimen followed by germline genetic testing and possibly further studies on the tumor. …
Lynch syndrome caused by defects in DNA mismatch repair genes, and diagnostic testing for Lynch syndrome begins with microsatellite instabil …
Inherited colorectal cancer syndromes.
Kastrinos F, Syngal S. Kastrinos F, et al. Cancer J. 2011 Nov-Dec;17(6):405-15. doi: 10.1097/PPO.0b013e318237e408. Cancer J. 2011. PMID: 22157284 Free PMC article. Review.
Most colorectal cancer cases diagnosed annually are due to sporadic events, but up to 5% are attributed to known monogenic disorders including Lynch syndrome, familial adenomatous polyposis, MYH-associated polyposis, and the rare hamartomatous polyposis syndr …
Most colorectal cancer cases diagnosed annually are due to sporadic events, but up to 5% are attributed to known monogenic disorders includi …
MYH polyposis syndrome: clinical findings, genetics issues and management.
Sereno M, Merino M, López-Gómez M, Gómez-Raposo C, Zambrana Tébar F, Moreno Rubio J, Espinós J, Martín-Algarra S, Casado Sáenz E. Sereno M, et al. Clin Transl Oncol. 2014 Aug;16(8):675-9. doi: 10.1007/s12094-014-1171-0. Epub 2014 Mar 19. Clin Transl Oncol. 2014. PMID: 24643704 Review.
In addition, some authors have indicated that the spectrum of extracolonic lesions in MYH associated polyposis (MAP) might be far different from that observed in FAP and could be more similar to Lynch syndrome spectrum. ...
In addition, some authors have indicated that the spectrum of extracolonic lesions in MYH associated polyposis (MAP) mi …
Hereditary colorectal cancer: MYH-associated polyposis and other newly identified disorders.
Lindor NM. Lindor NM. Best Pract Res Clin Gastroenterol. 2009;23(1):75-87. doi: 10.1016/j.bpg.2008.11.013. Best Pract Res Clin Gastroenterol. 2009. PMID: 19258188 Review.
In this paper, five topics relevant to genetic risk assessment for colorectal cancer are reviewed. These include the autosomal recessive MYH-associated polyposis, hyperplastic polyposis and serrated pathway syndrome, the association of autosomal dominant juve …
In this paper, five topics relevant to genetic risk assessment for colorectal cancer are reviewed. These include the autosomal recessive …
The "Studded" Rectum: Phenotypic Evidence of MYH-Associated Polyposis.
Church J, Kravochuck S. Church J, et al. Dis Colon Rectum. 2016 Jun;59(6):565-9. doi: 10.1097/DCR.0000000000000575. Dis Colon Rectum. 2016. PMID: 27145315 Clinical Trial.
BACKGROUND: MYH-associated polyposis is a recessively inherited syndrome of colorectal cancer predisposition attributed to biallelic germline mutations in the base excision repair gene MYH. Clinically it overlaps with attenuated familial adenomatous polyposis …
BACKGROUND: MYH-associated polyposis is a recessively inherited syndrome of colorectal cancer predisposition attributed …
Recently identified colon cancer predispositions: MYH and MSH6 mutations.
Kastrinos F, Syngal S. Kastrinos F, et al. Semin Oncol. 2007 Oct;34(5):418-24. doi: 10.1053/j.seminoncol.2007.07.005. Semin Oncol. 2007. PMID: 17920897 Free PMC article. Review.
However, additional syndromes continue to be defined and new predisposition genes are continuing to be identified. Most recently, MYH-associated polyposis (MAP) and an "atypical Lynch syndrome" related to the presence of MSH6 mutations have been linked to an …
However, additional syndromes continue to be defined and new predisposition genes are continuing to be identified. Most recently, MYH …
Colonic polyps in children and adolescents.
Durno CA. Durno CA. Can J Gastroenterol. 2007 Apr;21(4):233-9. doi: 10.1155/2007/401674. Can J Gastroenterol. 2007. PMID: 17431512 Free PMC article. Review.
Attenuated familial adenamatous polyposis (AFAP) can occur either by a mutation at the extreme ends of the adenomatous polyposis coli gene or by biallelic mutations in the mutY homologue (MYH) gene. The identification of MYH-associated polyposis as an autosom …
Attenuated familial adenamatous polyposis (AFAP) can occur either by a mutation at the extreme ends of the adenomatous polyposis coli gene o …
Prevalence of MYH-associated polyposis related to three recurrent mutations in Morocco.
Laarabi FZ, Cherkaoui Jaouad I, Benazzouz A, Squalli D, Sefiani A. Laarabi FZ, et al. Ann Hum Biol. 2011 May;38(3):360-3. doi: 10.3109/03014460.2010.521520. Epub 2010 Oct 13. Ann Hum Biol. 2011. PMID: 20939750
BACKGROUND: MYH-associated polyposis (MAP) is an autosomal recessive inherited disease. ...Recessively inherited mutations in the base excision repair gene MYH have recently been associated with predisposition to colorectal adenomas and cancer. The epidemiolo …
BACKGROUND: MYH-associated polyposis (MAP) is an autosomal recessive inherited disease. ...Recessively inherited mutati …
The multiple colorectal adenoma phenotype and MYH, a base excision repair gene.
Lipton L, Tomlinson I. Lipton L, et al. Clin Gastroenterol Hepatol. 2004 Aug;2(8):633-8. doi: 10.1016/s1542-3565(04)00286-1. Clin Gastroenterol Hepatol. 2004. PMID: 15290654 Review.
We summarize the genetic and clinical features of the colorectal adenomas and cancers that occur in MYH-associated polyposis (MAP). MAP results from biallelic germline mutations in the base excision repair gene, mutY homologue (MYH). ...
We summarize the genetic and clinical features of the colorectal adenomas and cancers that occur in MYH-associated polyposi …
Colorectal polyposes: from phenotype to diagnosis.
Jass JR. Jass JR. Pathol Res Pract. 2008;204(7):431-47. doi: 10.1016/j.prp.2008.03.008. Epub 2008 Jun 9. Pathol Res Pract. 2008. PMID: 18541388 Review.
The aim of this review is to highlight the principles and pitfalls in achieving a comprehensive description of the various types of colorectal polyposis, including classical FAP, attenuated FAP, MUTYH- (formerly MYH-) associated polyposis (MAP), other present …
The aim of this review is to highlight the principles and pitfalls in achieving a comprehensive description of the various types of colorect …
37 results