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

Year Number of Results
1948 1
1949 1
1950 2
1951 2
1952 4
1953 2
1954 1
1955 1
1956 3
1957 1
1959 1
1960 2
1961 1
1962 1
1963 4
1964 1
1965 2
1969 2
1970 1
1971 2
1972 2
1973 1
1974 5
1975 4
1976 5
1977 11
1978 12
1979 11
1980 14
1981 6
1982 5
1983 10
1984 19
1985 18
1986 20
1987 24
1988 17
1989 23
1990 22
1991 25
1992 36
1993 43
1994 49
1995 56
1996 36
1997 50
1998 80
1999 73
2000 74
2001 83
2002 52
2003 66
2004 60
2005 68
2006 68
2007 94
2008 74
2009 80
2010 110
2011 86
2012 108
2013 109
2014 115
2015 110
2016 96
2017 102
2018 93
2019 94
2020 105
2021 108
2022 119
2023 106
2024 89
2025 83

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2,825 results

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Page 1
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. ...Patients present benign and, malignant neoplasms in multiple organs, mostly breast and thyroid. The skin is the organ affected most consistently by …
PTEN hamartoma tumor syndrome (PTHS) includes diseases with germline pathogenic variants in the PTEN gene. ...Patients present …
Cowden's disease.
Bardenstein DS, McLean IW, Nerney J, Boatwright RS. Bardenstein DS, et al. Ophthalmology. 1988 Aug;95(8):1038-41. doi: 10.1016/s0161-6420(88)33066-6. Ophthalmology. 1988. PMID: 3068606 Review.
Cowden's disease, or multiple hamartoma syndrome, is a rare genodermatosis. Multiple facial trichilemmomas, acral keratoses, and oral papillomas are the most common mucocutaneous lesions in this disease. ...A case of Cowden'
Cowden's disease, or multiple hamartoma syndrome, is a rare genodermatosis. Multiple facial trichi
Thyroid disease associated with Cowden syndrome: A meta-analysis.
Hall JE, Abdollahian DJ, Sinard RJ. Hall JE, et al. Head Neck. 2013 Aug;35(8):1189-94. doi: 10.1002/hed.22971. Epub 2012 Mar 20. Head Neck. 2013. PMID: 22431287 Review.
BACKGROUND: We investigated the pathology and surgical management of thyroid disease in patients with Cowden syndrome (CS). METHODS: A query of the PubMed database between 2001 and January 2010 was performed using the terms "cowden syndrome OR …
BACKGROUND: We investigated the pathology and surgical management of thyroid disease in patients with Cowden syndrome ( …
Cowden disease: a review.
Uppal S, Mistry D, Coatesworth AP. Uppal S, et al. Int J Clin Pract. 2007 Apr;61(4):645-52. doi: 10.1111/j.1742-1241.2006.00896.x. Int J Clin Pract. 2007. PMID: 17394437 Review.
Cowden disease is a genetically inherited disorder presenting with multiple hamartomatous and neoplastic lesions in various organs and tissues. ...
Cowden disease is a genetically inherited disorder presenting with multiple hamartomatous and neoplastic lesions in var
Cowden's disease. A marker for malignancy.
Shapiro SD, Lambert WC, Schwartz RA. Shapiro SD, et al. Int J Dermatol. 1988 May;27(4):232-7. doi: 10.1111/j.1365-4362.1988.tb03214.x. Int J Dermatol. 1988. PMID: 3292446 Review. No abstract available.
Lhermitte-Duclos Disease Related With Cowden Syndrome Mimicking Metastatic Lung Cancer on FDG PET/CT.
Kesim S, Ozguven S, Oksuzoglu K, Erdil TY. Kesim S, et al. Clin Nucl Med. 2023 Feb 1;48(2):e99-e100. doi: 10.1097/RLU.0000000000004382. Epub 2022 Sep 6. Clin Nucl Med. 2023. PMID: 36607384
Cowden syndrome is characterized by multiple hamartomatous and neoplastic lesions including Lhermitte-Duclos disease, which is the main criterion for the diagnosis. ...Our case indicates that Cowden syndrome should be included as a differ
Cowden syndrome is characterized by multiple hamartomatous and neoplastic lesions including Lhermitte-Duclos disease
[Cowden disease].
Sawada T, Hamano N, Suzuki A, Okada T, Mabuchi H. Sawada T, et al. Nihon Rinsho. 2000 Jul;58(7):1479-83. Nihon Rinsho. 2000. PMID: 10921327 Review. Japanese.
Cowden disease is an autosomal dominant disorder associated with an increased risk of developing benign and malignant tumors in many organ systems including the breast, thyroid, skin, central nervous system and gastrointestinal tract. Recently, germline mutations in
Cowden disease is an autosomal dominant disorder associated with an increased risk of developing benign and malignant tumors i
Cowden disease.
Myung LK, Jo CS, Hyeok CJ, Moo YB, Baik HK, Hong KJ. Myung LK, et al. Gastrointest Endosc. 2006 Jan;63(1):151. doi: 10.1016/j.gie.2005.06.004. Gastrointest Endosc. 2006. PMID: 16377335 No abstract available.
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
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 establish …
BACKGROUND: PTEN hamartoma tumor syndrome (PHTS) refers to a spectrum of disorders caused by mutations in the phosphatase and …
2,825 results