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
1983 2
1988 2
1990 3
1991 2
1992 2
1993 2
1994 3
1995 4
1996 19
1997 4
1998 10
1999 6
2000 9
2001 6
2002 10
2003 4
2004 10
2005 18
2006 11
2007 6
2008 8
2009 12
2010 12
2011 6
2012 21
2013 12
2014 6
2015 13
2016 11
2017 18
2018 8
2019 9
2020 10
2021 7
2022 9
2023 8
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

284 results

Results by year

Filters applied: . Clear all
Page 1
[Lynch syndrome: What is new?].
Pellat A, Netter J, Perkins G, Cohen R, Coulet F, Parc Y, Svrcek M, Duval A, André T. Pellat A, et al. Bull Cancer. 2019 Jul-Aug;106(7-8):647-655. doi: 10.1016/j.bulcan.2018.10.009. Epub 2018 Dec 4. Bull Cancer. 2019. PMID: 30527816 Free article. Review. French.
Therefore, it is characterized by the predisposition to a spectrum of cancers, primarily colorectal cancer (CRC) and endometrial cancer (EC). Lynch syndrome-related CRC accounts for 3% of all CRC. Lynch syndrome also accounts for 2% of all EC. I …
Therefore, it is characterized by the predisposition to a spectrum of cancers, primarily colorectal cancer (CRC) and endometrial canc …
Identification of Lynch Syndrome.
Maratt JK, Stoffel E. Maratt JK, et al. Gastrointest Endosc Clin N Am. 2022 Jan;32(1):45-58. doi: 10.1016/j.giec.2021.09.002. Gastrointest Endosc Clin N Am. 2022. PMID: 34798986 Review.
Lynch syndrome (LS) is an autosomal dominant hereditary cancer syndrome caused by pathogenic germline variants (PGV) in any of the 4 DNA mismatch repair (MMR) genes, MLH1, MSH2, MSH6, and PMS2, or deletions in EPCAM. LS leads to an increased ris
Lynch syndrome (LS) is an autosomal dominant hereditary cancer syndrome caused by pathogenic germline variants (
Cystic Lung Diseases: Algorithmic Approach.
Raoof S, Bondalapati P, Vydyula R, Ryu JH, Gupta N, Raoof S, Galvin J, Rosen MJ, Lynch D, Travis W, Mehta S, Lazzaro R, Naidich D. Raoof S, et al. Chest. 2016 Oct;150(4):945-965. doi: 10.1016/j.chest.2016.04.026. Epub 2016 May 13. Chest. 2016. PMID: 27180915 Free PMC article. Review.
Multifocal/diffuse cysts can occur with lymphoid interstitial pneumonia, Birt-Hogg-Dube syndrome, tracheobronchial papillomatosis, or primary and metastatic cancers. ...
Multifocal/diffuse cysts can occur with lymphoid interstitial pneumonia, Birt-Hogg-Dube syndrome, tracheobronchial papillomatosis, or …
Mismatch Repair-Deficient Colorectal Cancer: Building on Checkpoint Blockade.
Jin Z, Sinicrope FA. Jin Z, et al. J Clin Oncol. 2022 Aug 20;40(24):2735-2750. doi: 10.1200/JCO.21.02691. Epub 2022 Jun 1. J Clin Oncol. 2022. PMID: 35649217 Free PMC article. Review.
Colorectal cancer (CRC) with deficient DNA mismatch repair (dMMR) is characterized by hypermutation leading to abundant neoantigens that activate an antitumor immune response in the tumor microenvironment. ...Accordingly, single-agent pembrolizumab represents a new standar
Colorectal cancer (CRC) with deficient DNA mismatch repair (dMMR) is characterized by hypermutation leading to abundant neoantigens t
Deficient mismatch repair/microsatellite unstable colorectal cancer: Diagnosis, prognosis and treatment.
Taieb J, Svrcek M, Cohen R, Basile D, Tougeron D, Phelip JM. Taieb J, et al. Eur J Cancer. 2022 Nov;175:136-157. doi: 10.1016/j.ejca.2022.07.020. Epub 2022 Sep 14. Eur J Cancer. 2022. PMID: 36115290 Review.
Nearly 30% of MSI CRCs occur in a context of constitutional mutation of the MMR system (Lynch syndrome). Others are sporadic cancers linked to a hypermethylation of the MLH-1 promoter. ...Indeed, recent data from prospective cohorts and randomised trials have shown …
Nearly 30% of MSI CRCs occur in a context of constitutional mutation of the MMR system (Lynch syndrome). Others are sporadic c …
Midbrain, Pons, and Medulla: Anatomy and Syndromes.
Sciacca S, Lynch J, Davagnanam I, Barker R. Sciacca S, et al. Radiographics. 2019 Jul-Aug;39(4):1110-1125. doi: 10.1148/rg.2019180126. Radiographics. 2019. PMID: 31283463 Review.
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.
A less aggressive variant of FAP, attenuated FAP (AFAP), is characterized by fewer colorectal adenomatous polyps (usually 10 to 100), later age of adenoma appearance and a lower cancer risk. ...Differential diagnoses include other disorders causing multiple polyps (such as …
A less aggressive variant of FAP, attenuated FAP (AFAP), is characterized by fewer colorectal adenomatous polyps (usually 10 to 100), …
AGA Clinical Practice Update on Pancreas Cancer Screening in High-Risk Individuals: Expert Review.
Aslanian HR, Lee JH, Canto MI. Aslanian HR, et al. Gastroenterology. 2020 Jul;159(1):358-362. doi: 10.1053/j.gastro.2020.03.088. Epub 2020 May 19. Gastroenterology. 2020. PMID: 32416142 Review.
BEST PRACTICE ADVICE 2: Pancreas cancer screening should be considered in patients with genetic syndromes associated with an increased risk of pancreas cancer, including all patients with Peutz-Jeghers syndrome, hereditary pancreatitis, patients with CDKN2A gene mut …
BEST PRACTICE ADVICE 2: Pancreas cancer screening should be considered in patients with genetic syndromes associated with an increased risk …
Lynch Syndrome and Endometrial Cancer.
Singh S, Resnick KE. Singh S, et al. South Med J. 2017 Apr;110(4):265-269. doi: 10.14423/SMJ.0000000000000633. South Med J. 2017. PMID: 28376523 Review.
In patients with Lynch syndrome, gynecologic cancer often can be the first presenting malignancy. In this review, we summarize the genetics of Lynch syndrome and review the various modalities of identifying patients at risk for this syndrome. .. …
In patients with Lynch syndrome, gynecologic cancer often can be the first presenting malignancy. In this review, we summarize …
An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy.
Kurland G, Deterding RR, Hagood JS, Young LR, Brody AS, Castile RG, Dell S, Fan LL, Hamvas A, Hilman BC, Langston C, Nogee LM, Redding GJ; American Thoracic Society Committee on Childhood Interstitial Lung Disease (chILD) and the chILD Research Network. Kurland G, et al. Am J Respir Crit Care Med. 2013 Aug 1;188(3):376-94. doi: 10.1164/rccm.201305-0923ST. Am J Respir Crit Care Med. 2013. PMID: 23905526 Free PMC article. Review.
These guidelines: (1) describe the clinical characteristics of neonates and infants (<2 yr of age) with diffuse lung disease (DLD); (2) list the common causes of DLD that should be eliminated during the evaluation of neonates and infants with DLD; (3) recommend methods for fur …
These guidelines: (1) describe the clinical characteristics of neonates and infants (<2 yr of age) with diffuse lung disease (DLD); (2) l …
284 results