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Items: 1 to 20 of 91

1.

More than just skin deep: faciocutaneous clues to genetic syndromes with malignancies.

Shen Z, Hoffman JD, Hao F, Pier E.

Oncologist. 2012;17(7):930-6. doi: 10.1634/theoncologist.2012-0033. Epub 2012 Jun 15. Review.

2.

Dermatological manifestations of inherited cancer syndromes in children.

Karalis A, Tischkowitz M, Millington GW.

Br J Dermatol. 2011 Feb;164(2):245-56. doi: 10.1111/j.1365-2133.2010.10100.x. Review.

PMID:
20973772
3.

Lessons from the skin--cutaneous features of familial cancer.

Winship IM, Dudding TE.

Lancet Oncol. 2008 May;9(5):462-72. doi: 10.1016/S1470-2045(08)70126-8. Review.

PMID:
18452857
4.

Faciocutaneous cancer syndromes: spot the diagnosis.

Morrison PJ, Ryan PD.

Oncologist. 2012;17(7):886-7. doi: 10.1634/theoncologist.2012-0171. Epub 2012 Jun 15. No abstract available.

5.

Muir-Torre Syndrome and founder mismatch repair gene mutations: A long gone historical genetic challenge.

Ponti G, Manfredini M, Tomasi A, Pellacani G.

Gene. 2016 Sep 10;589(2):127-32. doi: 10.1016/j.gene.2015.06.078. Epub 2015 Jul 2. Review.

PMID:
26143115
6.

Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic loci.

Stratakis CA, Kirschner LS, Taymans SE, Tomlinson IP, Marsh DJ, Torpy DJ, Giatzakis C, Eccles DM, Theaker J, Houlston RS, Blouin JL, Antonarakis SE, Basson CT, Eng C, Carney JA.

J Clin Endocrinol Metab. 1998 Aug;83(8):2972-6.

PMID:
9709978
7.
8.
9.

Oral mucosal stigmata in hereditary-cancer syndromes: From germline mutations to distinctive clinical phenotypes and tailored therapies.

Ponti G, Tomasi A, Manfredini M, Pellacani G.

Gene. 2016 May 10;582(1):23-32. doi: 10.1016/j.gene.2016.01.053. Epub 2016 Feb 3. Review.

PMID:
26850131
10.

Endocrine tumors associated with neurofibromatosis type 1, Peutz-Jeghers syndrome and other familial neoplasia syndromes.

Kalkan E, Waguespack SG.

Front Horm Res. 2013;41:166-81. doi: 10.1159/000345676. Epub 2013 Mar 19. Review.

PMID:
23652677
11.

Cancer-associated genodermatoses: skin neoplasms as clues to hereditary tumor syndromes.

Ponti G, Pellacani G, Seidenari S, Pollio A, Muscatello U, Tomasi A.

Crit Rev Oncol Hematol. 2013 Mar;85(3):239-56. doi: 10.1016/j.critrevonc.2012.07.001. Epub 2012 Jul 21. Review.

PMID:
22823951
12.

Genetic testing for cancer predisposition.

Eng C, Hampel H, de la Chapelle A.

Annu Rev Med. 2001;52:371-400. Review. Erratum in: Annu Rev Med 2002;53:xi.

PMID:
11160785
13.

Genodermatoses with malignant potential.

Holman JD, Dyer JA.

Curr Opin Pediatr. 2007 Aug;19(4):446-54. Review.

PMID:
17630610
14.

Thyroid cancer of follicular cell origin in inherited tumor syndromes.

Nosé V.

Adv Anat Pathol. 2010 Nov;17(6):428-36. doi: 10.1097/PAP.0b013e3181f8b028. Review.

PMID:
20966648
15.

[Cutaneous lesions in genetic tumor syndromes].

Christen-Zaech S, Vernez M.

Rev Med Suisse. 2008 Apr 30;4(155):1095-102. Review. French.

PMID:
18610722
16.

Muir-Torre syndrome.

Cohen PR, Kohn SR, Davis DA, Kurzrock R.

Dermatol Clin. 1995 Jan;13(1):79-89. Review.

PMID:
7712655
17.

Cancer-associated genodermatoses: a personal history.

Burgdorf WH.

Exp Dermatol. 2006 Sep;15(9):653-66. Review.

PMID:
16881962
18.

Familial skin cancer syndromes: Increased risk of nonmelanotic skin cancers and extracutaneous tumors.

Jaju PD, Ransohoff KJ, Tang JY, Sarin KY.

J Am Acad Dermatol. 2016 Mar;74(3):437-51; quiz 452-4. doi: 10.1016/j.jaad.2015.08.073. Review.

PMID:
26892653
19.

Hereditary syndromes predisposing to endocrine tumors and their skin manifestations.

Stratakis CA.

Rev Endocr Metab Disord. 2016 Sep;17(3):381-388. Review.

20.

Morphologic characterization of hamartomatous gastrointestinal polyps in Cowden syndrome, Peutz-Jeghers syndrome, and juvenile polyposis syndrome.

Shaco-Levy R, Jasperson KW, Martin K, Samadder NJ, Burt RW, Ying J, Bronner MP.

Hum Pathol. 2016 Mar;49:39-48. doi: 10.1016/j.humpath.2015.10.002. Epub 2015 Oct 31.

PMID:
26826408

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