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Results: 1 to 20 of 164

Similar articles for PubMed (Select 21822720)

1.

Acinic cell carcinoma of the retromolar trigone region: expanding the tumor phenotype in Cowden syndrome?

Villeneuve H, Tremblay S, Galiatsatos P, Hamel N, Guertin L, Morency R, Tischkowitz M.

Fam Cancer. 2011 Dec;10(4):691-4. doi: 10.1007/s10689-011-9472-8.

PMID:
21822720
2.

Male breast cancer in Cowden syndrome patients with germline PTEN mutations.

Fackenthal JD, Marsh DJ, Richardson AL, Cummings SA, Eng C, Robinson BG, Olopade OI.

J Med Genet. 2001 Mar;38(3):159-64.

3.

First report of ovarian dysgerminoma in Cowden syndrome with germline PTEN mutation and PTEN-related 10q loss of tumor heterozygosity.

Cho MY, Kim HS, Eng C, Kim DS, Kang SJ, Eom M, Yi SY, Bronner MP.

Am J Surg Pathol. 2008 Aug;32(8):1258-64. doi: 10.1097/PAS.0b013e31816be8b7.

PMID:
18594467
4.

Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation.

Marsh DJ, Coulon V, Lunetta KL, Rocca-Serra P, Dahia PL, Zheng Z, Liaw D, Caron S, Duboué B, Lin AY, Richardson AL, Bonnetblanc JM, Bressieux JM, Cabarrot-Moreau A, Chompret A, Demange L, Eeles RA, Yahanda AM, Fearon ER, Fricker JP, Gorlin RJ, Hodgson SV, Huson S, Lacombe D, Eng C, et al.

Hum Mol Genet. 1998 Mar;7(3):507-15.

5.

Germline PTEN mutations in Cowden syndrome-like families.

Marsh DJ, Dahia PL, Caron S, Kum JB, Frayling IM, Tomlinson IP, Hughes KS, Eeles RA, Hodgson SV, Murday VA, Houlston R, Eng C.

J Med Genet. 1998 Nov;35(11):881-5.

6.

Two distinct thyroid tumours in a patient with Cowden syndrome carrying both a 10q23 and a mitochondrial DNA germline deletion.

Pradella LM, Zuntini R, Magini P, Ceccarelli C, Neri I, Cerasoli S, Graziano C, Gasparre G, Turchetti D.

J Med Genet. 2011 Nov;48(11):779-82. doi: 10.1136/jmedgenet-2011-100152. Epub 2011 Sep 16.

PMID:
21926107
7.

Germline mutations in PTEN and SDHC in a woman with epithelial thyroid cancer and carotid paraganglioma.

Zbuk KM, Patocs A, Shealy A, Sylvester H, Miesfeldt S, Eng C.

Nat Clin Pract Oncol. 2007 Oct;4(10):608-12.

PMID:
17898811
8.

Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis.

Lynch ED, Ostermeyer EA, Lee MK, Arena JF, Ji H, Dann J, Swisshelm K, Suchard D, MacLeod PM, Kvinnsland S, Gjertsen BT, Heimdal K, Lubs H, Møller P, King MC.

Am J Hum Genet. 1997 Dec;61(6):1254-60.

9.

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome.

Liaw D, Marsh DJ, Li J, Dahia PL, Wang SI, Zheng Z, Bose S, Call KM, Tsou HC, Peacocke M, Eng C, Parsons R.

Nat Genet. 1997 May;16(1):64-7.

PMID:
9140396
10.

Cowden syndrome.

Gustafson S, Zbuk KM, Scacheri C, Eng C.

Semin Oncol. 2007 Oct;34(5):428-34. Review.

PMID:
17920899
11.

Analysis of PTEN gene mutations in Korean patients with Cowden syndrome and polyposis syndrome.

Kim DK, Myung SJ, Yang SK, Hong SS, Kim KJ, Byeon JS, Lee GH, Kim JH, Min YI, Lee SM, Jeong JY, Song K, Jung SA.

Dis Colon Rectum. 2005 Sep;48(9):1714-22.

PMID:
16007494
12.

Two novel mutations of PTEN gene in Japanese patients with Cowden syndrome.

Sawada T, Okada T, Miwa K, Satoh H, Asano A, Mabuchi H.

Am J Med Genet A. 2004 Jul 1;128A(1):12-4.

PMID:
15211648
13.

Evaluation of germline PTEN mutations in endometrial cancer patients.

Black D, Bogomolniy F, Robson ME, Offit K, Barakat RR, Boyd J.

Gynecol Oncol. 2005 Jan;96(1):21-4.

PMID:
15589575
14.

Germline mutations and variants in the succinate dehydrogenase genes in Cowden and Cowden-like syndromes.

Ni Y, Zbuk KM, Sadler T, Patocs A, Lobo G, Edelman E, Platzer P, Orloff MS, Waite KA, Eng C.

Am J Hum Genet. 2008 Aug;83(2):261-8. doi: 10.1016/j.ajhg.2008.07.011.

15.

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.

Marsh DJ, Kum JB, Lunetta KL, Bennett MJ, Gorlin RJ, Ahmed SF, Bodurtha J, Crowe C, Curtis MA, Dasouki M, Dunn T, Feit H, Geraghty MT, Graham JM Jr, Hodgson SV, Hunter A, Korf BR, Manchester D, Miesfeldt S, Murday VA, Nathanson KL, Parisi M, Pober B, Romano C, Eng C, et al.

Hum Mol Genet. 1999 Aug;8(8):1461-72.

16.

Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease.

Nelen MR, van Staveren WC, Peeters EA, Hassel MB, Gorlin RJ, Hamm H, Lindboe CF, Fryns JP, Sijmons RH, Woods DG, Mariman EC, Padberg GW, Kremer H.

Hum Mol Genet. 1997 Aug;6(8):1383-7.

17.

[Cowden syndrome, or multiple hamartomatous tumor syndrome, in clinical endocrinology].

Sardinoux M, Raingeard I, Bessis D, Coupier I, Renard E, Bringer J.

Ann Endocrinol (Paris). 2010 Sep;71(4):264-73. doi: 10.1016/j.ando.2010.04.001. French.

PMID:
20627233
18.

Skin abnormalities in individuals with macrocephaly: Cowden disease from a dermatologist's point of view.

van der Velden JJ, Vreeburg M, Smeets EE, Schrander-Stumpel CT, van Steensel MA.

Int J Dermatol. 2008 Nov;47 Suppl 1:45-8. doi: 10.1111/j.1365-4632.2008.03960.x.

PMID:
18986487
19.

Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome clinical features.

Pilarski R, Stephens JA, Noss R, Fisher JL, Prior TW.

J Med Genet. 2011 Aug;48(8):505-12. doi: 10.1136/jmg.2011.088807. Epub 2011 Jun 9.

PMID:
21659347
20.

Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in primary breast carcinomas.

Rhei E, Kang L, Bogomolniy F, Federici MG, Borgen PI, Boyd J.

Cancer Res. 1997 Sep 1;57(17):3657-9.

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