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
1989 1
1990 3
1991 2
1996 2
1999 1
2000 1
2001 1
2002 1
2003 3
2005 4
2006 4
2007 2
2008 2
2009 4
2010 2
2011 7
2012 3
2013 4
2014 7
2015 6
2016 6
2017 6
2018 10
2019 4
2020 5
2021 10
2022 7
2023 4
2024 4

Text availability

Article attribute

Article type

Publication date

Search Results

103 results

Results by year

Filters applied: . Clear all
Page 1
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. ...Patients with progressive tumors and unresectable disease may respond or …
A less aggressive variant of FAP, attenuated FAP (AFAP), is characterized by fewer colorectal adenomatous polyps (usually 10 to 100), …
Desmoid-Type Fibromatosis.
Garcia-Ortega DY, Martín-Tellez KS, Cuellar-Hubbe M, Martínez-Said H, Álvarez-Cano A, Brener-Chaoul M, Alegría-Baños JA, Martínez-Tlahuel JL. Garcia-Ortega DY, et al. Cancers (Basel). 2020 Jul 9;12(7):1851. doi: 10.3390/cancers12071851. Cancers (Basel). 2020. PMID: 32660036 Free PMC article. Review.
Desmoid tumors represent a rare entity of monoclonal origin characterized by locally aggressive behavior and inability to metastasize. ...This is a narrative review of this uncommon disease; we present current knowledge about molecular pathogenesis, diagnosis
Desmoid tumors represent a rare entity of monoclonal origin characterized by locally aggressive behavior and inability to meta
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.
The initiative of the 5th edition of the WHO classification of the Head and Neck Tumours establishing a new section dedicated to familial/heritable tumor syndromes with tumors and lesions in the head and neck region was much needed to better understand the tumours, diseases
The initiative of the 5th edition of the WHO classification of the Head and Neck Tumours establishing a new section dedicated to familial/he …
Management of Desmoid Disease in Familial Adenomatous Polyposis.
Sommovilla J, Shepard D, Liska D. Sommovilla J, et al. Clin Colon Rectal Surg. 2023 Jul 25;37(3):185-190. doi: 10.1055/s-0043-1770731. eCollection 2024 May. Clin Colon Rectal Surg. 2023. PMID: 38606047 Free PMC article. Review.
Desmoid disease impacts approximately 30% of FAP patients, with several known risk factors. ...Desmoid disease-directed therapy is individualized and impacted by desmoid stage, severity, postsurgical anatomy, and consequences of disease.
Desmoid disease impacts approximately 30% of FAP patients, with several known risk factors. ...Desmoid disease-d
Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.
Eccles DM, van der Luijt R, Breukel C, Bullman H, Bunyan D, Fisher A, Barber J, du Boulay C, Primrose J, Burn J, Fodde R. Eccles DM, et al. Am J Hum Genet. 1996 Dec;59(6):1193-201. Am J Hum Genet. 1996. PMID: 8940264 Free PMC article.
Here, we report hereditary desmoid disease (HDD), a novel autosomal dominant trait with 100% penetrance affecting a three-generation kindred. ...In general, one or more members in approximately 10% of the FAP families manifest desmoid tumors. Affected …
Here, we report hereditary desmoid disease (HDD), a novel autosomal dominant trait with 100% penetrance affecting a thr …
Desmoid tumors: diagnostic and therapeutic considerations.
Brener-Chaoul M, Cervantes-Gutiérrez Ó, Padilla-Longoria R, Martín-Téllez KS. Brener-Chaoul M, et al. Gac Med Mex. 2020;156(5):439-445. doi: 10.24875/GMM.M20000440. Gac Med Mex. 2020. PMID: 33372933 Review. English.
A literature review on desmoid tumors was carried out, which are tumors that affect soft tissues with a locally aggressive behavior and are unable to metastasize. Sporadic cases are located on the extremities and chest wall; hereditary cases have an intra-abd …
A literature review on desmoid tumors was carried out, which are tumors that affect soft tissues with a locally aggressive beh …
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.
Associated features include upper gastrointestinal tract polyps, congenital hypertrophy of the retinal pigment epithelium, desmoid tumors, and other extracolonic malignancies. Gardner syndrome is more of a historical subdivision of FAP, characterized by osteomas, dental an …
Associated features include upper gastrointestinal tract polyps, congenital hypertrophy of the retinal pigment epithelium, desmoid tu …
Hereditary desmoid disease in a family with a germline Alu I repeat mutation of the APC gene.
Halling KC, Lazzaro CR, Honchel R, Bufill JA, Powell SM, Arndt CA, Lindor NM. Halling KC, et al. Hum Hered. 1999 Mar;49(2):97-102. doi: 10.1159/000022852. Hum Hered. 1999. PMID: 10077730
We subsequently identified an Amish family with autosomal dominantly inherited desmoid tumors. Genetic analysis performed on one family member, a 47-year-old man with multiple desmoid tumors and no colon polyps, revealed a protein truncating mutation in the middle o …
We subsequently identified an Amish family with autosomal dominantly inherited desmoid tumors. Genetic analysis performed on one fami …
Chemoprevention in familial adenomatous polyposis: past, present and future.
Kemp Bohan PM, Mankaney G, Vreeland TJ, Chick RC, Hale DF, Cindass JL, Hickerson AT, Ensley DC, Sohn V, Clifton GT, Peoples GE, Burke CA. Kemp Bohan PM, et al. Fam Cancer. 2021 Jan;20(1):23-33. doi: 10.1007/s10689-020-00189-y. Epub 2020 Jun 8. Fam Cancer. 2021. PMID: 32507936 Free PMC article. Review.
However, colectomy is associated with morbidity and fails to prevent extra-colonic disease manifestations, including gastric polyposis, duodenal polyposis and cancer, thyroid cancer, and desmoid disease. Substantial research has investigated chemoprevention m …
However, colectomy is associated with morbidity and fails to prevent extra-colonic disease manifestations, including gastric polyposi …
Desmoid Tumor and Multiple Colon Adenomas.
Erickson LA, Chen B. Erickson LA, et al. Mayo Clin Proc. 2022 Jan;97(1):193-195. doi: 10.1016/j.mayocp.2021.11.025. Mayo Clin Proc. 2022. PMID: 34996557 No abstract available.
103 results