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Items: 1 to 20 of 429

1.

Peutz-Jeghers syndrome with intermittent upper intestinal obstruction: A case report and review of the literature.

Duan SX, Wang GH, Zhong J, Ou WH, Fu MX, Wang FS, Ma SH, Li JH.

Medicine (Baltimore). 2017 Apr;96(17):e6538. doi: 10.1097/MD.0000000000006538. Review.

2.

Mosaic Disorders of the PI3K/PTEN/AKT/TSC/mTORC1 Signaling Pathway.

Nathan N, Keppler-Noreuil KM, Biesecker LG, Moss J, Darling TN.

Dermatol Clin. 2017 Jan;35(1):51-60. doi: 10.1016/j.det.2016.07.001. Review.

PMID:
27890237
3.

Cowden Syndrome: Serendipitous Diagnosis in Patients with Significant Breast Disease. Case Series and Literature Review.

Heaney RM, Farrell M, Stokes M, Gorey T, Murray D.

Breast J. 2017 Jan;23(1):90-94. doi: 10.1111/tbj.12691. Epub 2016 Nov 25. Review.

PMID:
27886412
4.

Overgrowth syndromes with vascular malformations.

Hagen SL, Hook KP.

Semin Cutan Med Surg. 2016 Sep;35(3):161-9. doi: 10.12788/j.sder.2016.049. Review.

PMID:
27607325
5.

Heritable Gastrointestinal Cancer Syndromes.

Stoffel EM.

Gastroenterol Clin North Am. 2016 Sep;45(3):509-27. doi: 10.1016/j.gtc.2016.04.008. Review.

PMID:
27546846
6.

Multi-organ benign and malignant tumors: recognizing Cowden syndrome: a case report and review of the literature.

Gosein MA, Narinesingh D, Nixon CA, Goli SR, Maharaj P, Sinanan A.

BMC Res Notes. 2016 Aug 4;9:388. doi: 10.1186/s13104-016-2195-z. Review.

7.

Testing for Hereditary Predisposition in Patients with Gynecologic Cancers, Quo Vadis?

Mitchell G, Schrader KA.

Surg Pathol Clin. 2016 Jun;9(2):301-6. doi: 10.1016/j.path.2016.01.009. Epub 2016 Apr 11. Review.

PMID:
27241110
8.

Gynecologic Manifestations of Less Commonly Encountered Hereditary Syndromes.

DeLair DF, Soslow RA.

Surg Pathol Clin. 2016 Jun;9(2):269-87. doi: 10.1016/j.path.2016.01.008. Epub 2016 Apr 11. Review.

PMID:
27241108
9.

Cutaneous manifestations of breast cancer.

Tan AR.

Semin Oncol. 2016 Jun;43(3):331-4. doi: 10.1053/j.seminoncol.2016.02.030. Epub 2016 Feb 23. Review.

PMID:
27178684
10.

Proliferative lesion of anogenital mammary-like glands in the setting of Cowden syndrome: case report and review of the literature.

Hedayat AA, Pettus JR, Marotti JD, Tafe LJ, Holubar SD, Lisovsky M.

J Cutan Pathol. 2016 Aug;43(8):707-10. doi: 10.1111/cup.12721. Epub 2016 May 9. Review.

PMID:
27090873
11.

[Rare hereditary syndromes associated with polyposis and the development of malignant tumors].

Kazubskaya TP, Kozlova VM, Filippova MG, Тrofimov EI, Belev NF, Sokolova IN, Tamrazov RI, Pavlovskaya AI, Kondratyeva TT.

Arkh Patol. 2016 Mar-Apr;78(2):10-18. doi: 10.17116/patol201678210-18. Review. Russian.

PMID:
27070770
12.

Low-Flow Vascular Malformation Pitfalls: From Clinical Examination to Practical Imaging Evaluation--Part 2, Venous Malformation Mimickers.

Olivieri B, White CL, Restrepo R, McKeon B, Karakas SP, Lee EY.

AJR Am J Roentgenol. 2016 May;206(5):952-62. doi: 10.2214/AJR.15.15794. Epub 2016 Mar 21. Review.

PMID:
26999647
13.
14.

Managing patients at genetic risk of breast cancer.

Pederson HJ, Padia SA, May M, Grobmyer S.

Cleve Clin J Med. 2016 Mar;83(3):199-206. doi: 10.3949/ccjm.83a.14057. Review.

15.

Hereditary non-BRCA gynecological tumors.

Vellone VG, Paudice M, Varesco L.

Minerva Ginecol. 2016 Oct;68(5):579-86. Epub 2016 Mar 1. Review.

PMID:
26930387
16.

Cutaneous and ocular manifestations of neurocutaneous syndromes.

Chernoff KA, Schaffer JV.

Clin Dermatol. 2016 Mar-Apr;34(2):183-204. doi: 10.1016/j.clindermatol.2015.11.003. Epub 2015 Nov 22. Review.

PMID:
26903185
17.

Clinical and molecular features of young-onset colorectal cancer.

Ballester V, Rashtak S, Boardman L.

World J Gastroenterol. 2016 Feb 7;22(5):1736-44. doi: 10.3748/wjg.v22.i5.1736. Review.

18.

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
19.

Inherited PTEN mutations and the prediction of phenotype.

Leslie NR, Longy M.

Semin Cell Dev Biol. 2016 Apr;52:30-8. doi: 10.1016/j.semcdb.2016.01.030. Epub 2016 Jan 28. Review.

20.

The spectrum of nephrocutaneous diseases and associations: Genetic causes of nephrocutaneous disease.

Wofford J, Fenves AZ, Jackson JM, Kimball AB, Menter A.

J Am Acad Dermatol. 2016 Feb;74(2):231-44; quiz 245-6. doi: 10.1016/j.jaad.2015.05.039. Review.

PMID:
26775773

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