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

Year Number of Results
1971 1
1976 1
1977 1
1978 3
1985 2
1986 1
1987 2
1988 7
1989 3
1990 4
1991 4
1992 9
1993 10
1994 16
1995 11
1996 8
1997 7
1998 13
1999 16
2000 12
2001 23
2002 15
2003 9
2004 17
2005 12
2006 16
2007 13
2008 13
2009 18
2010 11
2011 12
2012 18
2013 15
2014 17
2015 23
2016 18
2017 17
2018 7
2019 20
2020 22
2021 18
2022 10
2023 7
2024 4

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456 results

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Page 1
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 po …
Between 2 and 5% of all CRCs occur due to inherited syndromes, including Lynch syndrome, familial adenomatous polyposis, MUTYH-associ …
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.
Genetic testing should be conducted in the context of pre- and post-test genetic counseling to ensure the patient's informed decision making. Patients who meet clinical criteria for a syndrome as well as those with identified pathogenic germline mutations should receive ap …
Genetic testing should be conducted in the context of pre- and post-test genetic counseling to ensure the patient's informed decision making …
Cowden syndrome and the PTEN hamartoma tumor syndrome: systematic review and revised diagnostic criteria.
Pilarski R, Burt R, Kohlman W, Pho L, Shannon KM, Swisher E. Pilarski R, et al. J Natl Cancer Inst. 2013 Nov 6;105(21):1607-16. doi: 10.1093/jnci/djt277. Epub 2013 Oct 17. J Natl Cancer Inst. 2013. PMID: 24136893 Review.
BACKGROUND: PTEN hamartoma tumor syndrome (PHTS) refers to a spectrum of disorders caused by mutations in the phosphatase and tensin homolog (PTEN) gene. Diagnostic criteria for Cowden syndrome, the principal PTEN-related disorder, were first established in 1 …
BACKGROUND: PTEN hamartoma tumor syndrome (PHTS) refers to a spectrum of disorders caused by mutations in the phosphatase and …
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-Spiegl …
This review highlights the important findings within these syndromes, especially on the update on syndromes with tumors involving the head a …
An update on the CNS manifestations of neurofibromatosis type 2.
Coy S, Rashid R, Stemmer-Rachamimov A, Santagata S. Coy S, et al. Acta Neuropathol. 2020 Apr;139(4):643-665. doi: 10.1007/s00401-019-02029-5. Epub 2019 Jun 4. Acta Neuropathol. 2020. PMID: 31161239 Free PMC article. Review.
Neurofibromatosis type II (NF2) is a tumor predisposition syndrome characterized by the development of distinctive nervous system lesions. ...NF2 has a highly variable clinical course, with some patients exhibiting a severe phenotype and development of multiple tumo …
Neurofibromatosis type II (NF2) is a tumor predisposition syndrome characterized by the development of distinctive nervous system les …
Cowden syndrome.
Farooq A, Walker LJ, Bowling J, Audisio RA. Farooq A, et al. Cancer Treat Rev. 2010 Dec;36(8):577-83. doi: 10.1016/j.ctrv.2010.04.002. Epub 2010 May 23. Cancer Treat Rev. 2010. PMID: 20580873 Review.
Cowden syndrome (CS) is a rare inherited condition characterised by multiple hamartomas in a variety of tissues from all three embryonic layers. It is a cancer predisposition syndrome with an increased risk of developing malignancy in many tissues but especia …
Cowden syndrome (CS) is a rare inherited condition characterised by multiple hamartomas in a variety of tissues from all three …
Cowden Disease: A Review.
Magaña M, Landeta-Sa AP, López-Flores Y. Magaña M, et al. Am J Dermatopathol. 2022 Oct 1;44(10):705-717. doi: 10.1097/DAD.0000000000002234. Am J Dermatopathol. 2022. PMID: 36122333 Review.
PTEN hamartoma tumor syndrome (PTHS) includes diseases with germline pathogenic variants in the PTEN gene. Cowden syndrome is included in this syndrome . PTEN (phosphatase and tensin homolog) is a tumor suppressor gene located on chromosome 10q22-23; n …
PTEN hamartoma tumor syndrome (PTHS) includes diseases with germline pathogenic variants in the PTEN gene. Cowden syndrome …
Cowden syndrome.
Gustafson S, Zbuk KM, Scacheri C, Eng C. Gustafson S, et al. Semin Oncol. 2007 Oct;34(5):428-34. doi: 10.1053/j.seminoncol.2007.07.009. Semin Oncol. 2007. PMID: 17920899 Review.
Germline PTEN mutations also are associated with syndromes that have not been historically connected to an increase in risk for malignancy. These disorders include Bannayan-Riley-Ruvalcaba syndrome (BRRS), Proteus syndrome (PS), and Proteus-like syndrome (PSL …
Germline PTEN mutations also are associated with syndromes that have not been historically connected to an increase in risk for malignancy. …
Hamartomatous polyps: Diagnosis, surveillance, and management.
Gorji L, Albrecht P. Gorji L, et al. World J Gastroenterol. 2023 Feb 28;29(8):1304-1314. doi: 10.3748/wjg.v29.i8.1304. World J Gastroenterol. 2023. PMID: 36925460 Free PMC article. Review.
Hereditary polyposis syndrome can be divided into three categories: Ade-nomatous, serrated, and hamartomatous polyps. ...These syndromes exhibit hamartomatous gastrointestinal polyps in conjunction to extra-intestinal manifestations, which require conscientious and diligen …
Hereditary polyposis syndrome can be divided into three categories: Ade-nomatous, serrated, and hamartomatous polyps. ...These syndro …
Cowden syndrome.
Hanssen AM, Fryns JP. Hanssen AM, et al. J Med Genet. 1995 Feb;32(2):117-9. doi: 10.1136/jmg.32.2.117. J Med Genet. 1995. PMID: 7760320 Free PMC article. Review.
Cowden syndrome, or the multiple hamartoma syndrome, is a familial cancer syndrome with involvement of various organ systems. ...Progressive macrocephaly, scrotal tongue, and mild to moderate mental retardation are important signs indicating the …
Cowden syndrome, or the multiple hamartoma syndrome, is a familial cancer syndrome with involvement of va …
456 results