PubMed (cited) for id: 158320

Year	Number of Results
1967	1
1968	1
1973	1
1974	2
1976	2
1977	1
1980	1
1981	1
1982	1
1984	1
1985	1
1986	1
1990	1
1991	2
1992	1
1993	1
1994	2
1995	1
1996	2
1998	1
1999	1
2000	1
2001	1
2002	1
2004	2
2005	1
2014	1
2024	0

1

A clinical scoring system to identify patients with sebaceous neoplasms at risk for the Muir-Torre variant of Lynch syndrome.

Roberts ME, Riegert-Johnson DL, Thomas BC, Rumilla KM, Thomas CS, Heckman MG, Purcell JU, Hanson NB, Leppig KA, Lim J, Cappel MA. Roberts ME, et al. Genet Med. 2014 Sep;16(9):711-6. doi: 10.1038/gim.2014.19. Epub 2014 Mar 6. Genet Med. 2014. PMID: 24603434 Free article.

2

Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomas: role of clinical features, microsatellite instability, and immunohistochemistry.

Ponti G, Losi L, Di Gregorio C, Roncucci L, Pedroni M, Scarselli A, Benatti P, Seidenari S, Pellacani G, Lembo L, Rossi G, Marino M, Lucci-Cordisco E, Ponz de Leon M. Ponti G, et al. Cancer. 2005 Mar 1;103(5):1018-25. doi: 10.1002/cncr.20873. Cancer. 2005. PMID: 15662714 Free article.

3

A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome.

Mangold E, Pagenstecher C, Leister M, Mathiak M, Rütten A, Friedl W, Propping P, Ruzicka T, Kruse R. Mangold E, et al. J Med Genet. 2004 Jul;41(7):567-72. doi: 10.1136/jmg.2003.012997. J Med Genet. 2004. PMID: 15235030 Free PMC article. No abstract available.

4

Spectrum of genetic alterations in Muir-Torre syndrome is the same as in HNPCC.

Barana D, van der Klift H, Wijnen J, Longa ED, Radice P, Cetto GL, Fodde R, Oliani C. Barana D, et al. Am J Med Genet A. 2004 Mar 15;125A(3):318-9. doi: 10.1002/ajmg.a.20523. Am J Med Genet A. 2004. PMID: 14994245 No abstract available.

5

Loss of fragile histidine triad (FHIT) expression and microsatellite instability in periocular sebaceous gland carcinoma in patients with Muir-Torre syndrome.

Holbach LM, von Moller A, Decker C, Jünemann AG, Rummelt-Hofmann C, Ballhausen WG. Holbach LM, et al. Am J Ophthalmol. 2002 Jul;134(1):147-8. doi: 10.1016/s0002-9394(02)01434-4. Am J Ophthalmol. 2002. PMID: 12095833

6

"Second hit" in sebaceous tumors from Muir-Torre patients with germline mutations in MSH2: allele loss is not the preferred mode of inactivation.

Kruse R, Rütten A, Hosseiny-Malayeri HR, Bisceglia M, Friedl W, Propping P, Ruzicka T, Mangold E. Kruse R, et al. J Invest Dermatol. 2001 Mar;116(3):463-5. doi: 10.1046/j.1523-1747.2001.01265.x. J Invest Dermatol. 2001. PMID: 11231323 Free article.

7

Muir-Torre-like syndrome in Fhit-deficient mice.

Fong LY, Fidanza V, Zanesi N, Lock LF, Siracusa LD, Mancini R, Siprashvili Z, Ottey M, Martin SE, Druck T, McCue PA, Croce CM, Huebner K. Fong LY, et al. Proc Natl Acad Sci U S A. 2000 Apr 25;97(9):4742-7. doi: 10.1073/pnas.080063497. Proc Natl Acad Sci U S A. 2000. PMID: 10758156 Free PMC article.

8

Muir-Torre syndrome: case report of a patient with concurrent jejunal and ureteral cancer and a review of the literature.

Akhtar S, Oza KK, Khan SA, Wright J. Akhtar S, et al. J Am Acad Dermatol. 1999 Nov;41(5 Pt 1):681-6. doi: 10.1016/s0190-9622(99)70001-0. J Am Acad Dermatol. 1999. PMID: 10534628 Free article. Review.

9

Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria.

Kruse R, Rütten A, Lamberti C, Hosseiny-Malayeri HR, Wang Y, Ruelfs C, Jungck M, Mathiak M, Ruzicka T, Hartschuh W, Bisceglia M, Friedl W, Propping P. Kruse R, et al. Am J Hum Genet. 1998 Jul;63(1):63-70. doi: 10.1086/301926. Am J Hum Genet. 1998. PMID: 9634524 Free PMC article.

10

Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?

Kruse R, Lamberti C, Wang Y, Ruelfs C, Bruns A, Esche C, Lehmann P, Ruzicka T, Rütten A, Friedl W, Propping P. Kruse R, et al. Hum Genet. 1996 Dec;98(6):747-50. doi: 10.1007/s004390050298. Hum Genet. 1996. PMID: 8931714

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