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

Year Number of Results
1993 1
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1998 36
1999 23
2000 26
2001 27
2002 15
2003 18
2004 19
2005 16
2006 25
2007 30
2008 25
2009 17
2010 33
2011 39
2012 49
2013 50
2014 48
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761 results
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Page 1
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, …
BACKGROUND: PTEN hamartoma tumor syndrome (PHTS) refers to a spectrum of disorders caused by mutations in the phosphata …
PTEN Hamartoma tumor syndrome in childhood: A review of the clinical literature.
Macken WL, Tischkowitz M, Lachlan KL. Macken WL, et al. Am J Med Genet C Semin Med Genet. 2019 Dec;181(4):591-610. doi: 10.1002/ajmg.c.31743. Epub 2019 Oct 14. Am J Med Genet C Semin Med Genet. 2019. PMID: 31609537 Review.
PTEN hamartoma tumor syndrome (PHTS) is a highly variable autosomal dominant condition associated with intellectual disability, overgrowth, and tumor predisposition phenotypes, which often overlap. PHTS incorporates a number of historical clinical presentatio …
PTEN hamartoma tumor syndrome (PHTS) is a highly variable autosomal dominant condition associated with intellectual dis …
WWP1 Gain-of-Function Inactivation of PTEN in Cancer Predisposition.
Lee YR, Yehia L, Kishikawa T, Ni Y, Leach B, Zhang J, Panch N, Liu J, Wei W, Eng C, Pandolfi PP. Lee YR, et al. N Engl J Med. 2020 May 28;382(22):2103-2116. doi: 10.1056/NEJMoa1914919. N Engl J Med. 2020. PMID: 32459922 Free PMC article.
BACKGROUND: Patients with PTEN hamartoma tumor syndrome (PHTS) have germline mutations in the tumor-suppressor gene encoding phosphatase and tensin homologue (PTEN). Such mutations have been associated with a hereditary predisposition to multiple …
BACKGROUND: Patients with PTEN hamartoma tumor syndrome (PHTS) have germline mutations in the tumor-suppressor gene enc …
Cowden Disease.
Garofola C, Jamal Z, Gross GP. Garofola C, et al. 2022 Jul 24. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2023 Jan–. 2022 Jul 24. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2023 Jan–. PMID: 30252240 Free Books & Documents.
Cowden disease, also known as Cowden syndrome or multiple hamartoma syndrome, is a genodermatosis originally described in 1963 by Lloyd and Dennis. ...Characteristically, patients with Cowden syndrome develop mucocuta …
Cowden disease, also known as Cowden syndrome or multiple hamartoma syndrome, is a genoderm …
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 locat …
PTEN hamartoma tumor syndrome (PTHS) includes diseases with germline pathogenic variants in the PTEN gene. Co …
High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome.
Bubien V, Bonnet F, Brouste V, Hoppe S, Barouk-Simonet E, David A, Edery P, Bottani A, Layet V, Caron O, Gilbert-Dussardier B, Delnatte C, Dugast C, Fricker JP, Bonneau D, Sevenet N, Longy M, Caux F; French Cowden Disease Network. Bubien V, et al. J Med Genet. 2013 Apr;50(4):255-63. doi: 10.1136/jmedgenet-2012-101339. Epub 2013 Jan 18. J Med Genet. 2013. PMID: 23335809 Free article.
BACKGROUND: PTEN hamartoma tumour syndrome (PHTS) encompasses several clinical syndromes with germline mutations in the PTEN tumour suppressor gene, including Cowden syndrome which is characterised by an increased risk of breast and thyro …
BACKGROUND: PTEN hamartoma tumour syndrome (PHTS) encompasses several clinical syndromes with germline mutations in the …
Germline mutation of the PTEN gene in a Japanese patient with Cowden's disease.
Kato N, Kimura K, Sugawara H, Aoyagi S, Ikeda T, Horii A. Kato N, et al. Int J Oncol. 2001 May;18(5):1017-22. doi: 10.3892/ijo.18.5.1017. Int J Oncol. 2001. PMID: 11295050 Review.
Cowden's disease (CD) is an autosomal dominant disorder which confers a high susceptibility to diverse benign and malignant tumors. ...Recently, germline mutations of this gene were also found in patients with CD, and it is now recognized as a gene responsible for t …
Cowden's disease (CD) is an autosomal dominant disorder which confers a high susceptibility to diverse benign and malignant tu …
PTEN in Hereditary and Sporadic Cancer.
Ngeow J, Eng C. Ngeow J, et al. Cold Spring Harb Perspect Med. 2020 Apr 1;10(4):a036087. doi: 10.1101/cshperspect.a036087. Cold Spring Harb Perspect Med. 2020. PMID: 31570378 Free PMC article. Review.
Germline pathogenic phosphatase and tensin homolog (PTEN) mutations cause PTEN hamartoma tumor syndrome (PHTS), characterized by various benign and malignant tumors of the thyroid, breast, endometrium, and other organs. ...In this review, we highlight …
Germline pathogenic phosphatase and tensin homolog (PTEN) mutations cause PTEN hamartoma tumor syndrome (PHTS), …
Gastrointestinal manifestations in PTEN hamartoma tumor syndrome.
D'Ermo G, Genuardi M. D'Ermo G, et al. Best Pract Res Clin Gastroenterol. 2022 Jun-Aug;58-59:101792. doi: 10.1016/j.bpg.2022.101792. Epub 2022 Mar 17. Best Pract Res Clin Gastroenterol. 2022. PMID: 35988965 Review.
The PTEN hamartoma tumor syndrome (PHTS) is a heterogeneous set of multisystem disorders caused by germline pathogenic variants in the PTEN tumor suppressor gene. ...Evidence of involvement of the GI tract has accrued over time, leading to the incorpor …
The PTEN hamartoma tumor syndrome (PHTS) is a heterogeneous set of multisystem disorders caused by germline pathogenic …
Brain 18F-FDG PET in Cowden Syndrome.
Grangeret J, Frismand S, Muller M, Renaud M, Verger A. Grangeret J, et al. Clin Nucl Med. 2022 Feb 1;47(2):e118-e119. doi: 10.1097/RLU.0000000000004025. Clin Nucl Med. 2022. PMID: 35006113
Cowden disease is associated with neurodevelopmental abnormalities such as macrocephaly, autism spectrum disorder, and developmental delay. ...Our current communication extends the neurological Cowden syndrome phenotype by using brain 18F-FDG PET/CT im …
Cowden disease is associated with neurodevelopmental abnormalities such as macrocephaly, autism spectrum disorder, and develop …
761 results