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Journal Abstract Search

138 related items for PubMed ID: 16632275

  • 1. Cowden syndrome: report of a case with immunohistochemical analysis and review of the literature.
    Scheper MA, Nikitakis NG, Sarlani E, Sauk JJ, Meiller TF.
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2006 May; 101(5):625-31. PubMed ID: 16632275
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  • 2. Cowden syndrome: report of two cases with immunohistochemical analysis for PTEN expression.
    Zabetian S, Mehregan D.
    Am J Dermatopathol; 2012 Aug; 34(6):632-4. PubMed ID: 22481496
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  • 3. [Cowden disease].
    Sawada T, Hamano N, Suzuki A, Okada T, Mabuchi H.
    Nihon Rinsho; 2000 Jul; 58(7):1479-83. PubMed ID: 10921327
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  • 6. Esophageal cancer in a family with hamartomatous tumors and germline PTEN frameshift and SMAD7 missense mutations.
    Sherman SK, Maxwell JE, Qian Q, Bellizzi AM, Braun TA, Iannettoni MD, Darbro BW, Howe JR.
    Cancer Genet; 2015 Jul; 208(1-2):41-6. PubMed ID: 25554686
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  • 8. Multiple sclerotic fibromas of the skin: an important clue for the diagnosis of Cowden syndrome.
    Kieselova K, Santiago F, Henrique M, Cunha MF.
    BMJ Case Rep; 2017 Aug 28; 2017():. PubMed ID: 28847996
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  • 9. Novel Germline PTEN Mutation Associated with Cowden Syndrome and Osteosarcoma.
    Lopez C, Abuel-Haija M, Pena L, Coppola D.
    Cancer Genomics Proteomics; 2018 Aug 28; 15(2):115-120. PubMed ID: 29496690
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  • 14. 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 01; 57(17):3657-9. PubMed ID: 9288766
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  • 18. Cowden syndrome.
    Farooq A, Walker LJ, Bowling J, Audisio RA.
    Cancer Treat Rev; 2010 Dec 01; 36(8):577-83. PubMed ID: 20580873
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  • 19. PTEN hamartoma tumor syndrome.
    Mester J, Charis E.
    Handb Clin Neurol; 2015 Dec 01; 132():129-37. PubMed ID: 26564076
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  • 20. 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 01; 16(1):64-7. PubMed ID: 9140396
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