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22. Lhermitte-Duclos disease caused by a novel germline PTEN mutation R173P in a patient presenting with psychosis. Kirches E; Steiner J; Schneider T; Vorwerk CK; Scherlach C; Holtkamp N; Keilhoff G; Eng C; Mawrin C Neuropathol Appl Neurobiol; 2010 Feb; 36(1):86-9. PubMed ID: 19719509 [No Abstract] [Full Text] [Related]
23. KILLIN gene discovery stirs up research on Cowden syndrome cancers. Schmidt C J Natl Cancer Inst; 2011 Mar; 103(5):362-4. PubMed ID: 21357597 [No Abstract] [Full Text] [Related]
24. Multiple keratotic papules and plaques on the trunk in Cowden's disease with MALT lymphoma. Mizuno S; Takeichi T; Sato J; Nakamura M; Goto H; Sugiura K; Akiyama M J Dermatol; 2018 Feb; 45(2):238-240. PubMed ID: 28391632 [No Abstract] [Full Text] [Related]
25. 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. PubMed ID: 18594467 [TBL] [Abstract][Full Text] [Related]
26. Identification of a novel PTEN mutation (L139X) in a patient with Cowden disease and Sjögren's syndrome. Raizis AM; Ferguson MM; Robinson BA; Atkinson CH; George PM Mol Pathol; 1998 Dec; 51(6):339-41. PubMed ID: 10193515 [TBL] [Abstract][Full Text] [Related]
27. The spectrum of vascular anomalies in patients with PTEN mutations: implications for diagnosis and management. Tan WH; Baris HN; Burrows PE; Robson CD; Alomari AI; Mulliken JB; Fishman SJ; Irons MB J Med Genet; 2007 Sep; 44(9):594-602. PubMed ID: 17526801 [TBL] [Abstract][Full Text] [Related]
28. Cowden syndrome: a rare, but recognisable cancer predisposition disorder. Adlard JW Clin Oncol (R Coll Radiol); 2005 Aug; 17(5):393. PubMed ID: 16097574 [No Abstract] [Full Text] [Related]
29. Association of multiple vertebral hemangiomas and severe paraparesis in a patient with a PTEN hamartoma tumor syndrome. Case report. Jenny B; Radovanovic I; Haenggeli CA; Delavelle J; Rüfenacht D; Kaelin A; Blouin JL; Bottani A; Rilliet B J Neurosurg; 2007 Oct; 107(4 Suppl):307-13. PubMed ID: 17941496 [TBL] [Abstract][Full Text] [Related]
30. Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease. Arch EM; Goodman BK; Van Wesep RA; Liaw D; Clarke K; Parsons R; McKusick VA; Geraghty MT Am J Med Genet; 1997 Sep; 71(4):489-93. PubMed ID: 9286463 [TBL] [Abstract][Full Text] [Related]
36. A novel PTEN mutation in Cowden syndrome is associated with a mixed degenerative-erosive arthritic process: potential molecular pathogenic mechanisms. Pinzone JJ; Eng C; Paik J; Brindle KA; Ringel MD; Katz JD Am J Med Genet A; 2007 Jul; 143A(13):1522-7. PubMed ID: 17568419 [No Abstract] [Full Text] [Related]
37. A longitudinally extensive myelopathy associated with multiple spinal arteriovenous fistulas in a patient with Cowden syndrome: a case report. Barreras P; Gailloud P; Pardo CA Spine J; 2018 Jan; 18(1):e1-e5. PubMed ID: 26795104 [TBL] [Abstract][Full Text] [Related]
38. PTEN and inherited hamartoma-cancer syndromes. Eng C; Peacocke M Nat Genet; 1998 Jul; 19(3):223. PubMed ID: 9662392 [No Abstract] [Full Text] [Related]
39. Variant manifestation of Cowden disease in Japan: hamartomatous polyposis of the digestive tract with mutation of the PTEN gene. Kurose K; Araki T; Matsunaka T; Takada Y; Emi M Am J Hum Genet; 1999 Jan; 64(1):308-10. PubMed ID: 9915974 [No Abstract] [Full Text] [Related]
40. Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTEN. Celebi JT; Tsou HC; Chen FF; Zhang H; Ping XL; Lebwohl MG; Kezis J; Peacocke M J Med Genet; 1999 May; 36(5):360-4. PubMed ID: 10353779 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]