273 related articles for article (PubMed ID: 8673088)
1. Localization of the gene for Cowden disease to chromosome 10q22-23.
Nelen MR; Padberg GW; Peeters EA; Lin AY; van den Helm B; Frants RR; Coulon V; Goldstein AM; van Reen MM; Easton DF; Eeles RA; Hodgsen S; Mulvihill JJ; Murday VA; Tucker MA; Mariman EC; Starink TM; Ponder BA; Ropers HH; Kremer H; Longy M; Eng C
Nat Genet; 1996 May; 13(1):114-6. PubMed ID: 8673088
[TBL] [Abstract][Full Text] [Related]
2. Cowden disease or multiple hamartoma syndrome--cutaneous clue to internal malignancy.
Fistarol SK; Anliker MD; Itin PH
Eur J Dermatol; 2002; 12(5):411-21. PubMed ID: 12370126
[TBL] [Abstract][Full Text] [Related]
3. Lhermitte-Duclos disease and Cowden disease: a single phakomatosis.
Padberg GW; Schot JD; Vielvoye GJ; Bots GT; de Beer FC
Ann Neurol; 1991 May; 29(5):517-23. PubMed ID: 1859181
[TBL] [Abstract][Full Text] [Related]
4. Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome.
Marsh DJ; Roth S; Lunetta KL; Hemminki A; Dahia PL; Sistonen P; Zheng Z; Caron S; van Orsouw NJ; Bodmer WF; Cottrell SE; Dunlop MG; Eccles D; Hodgson SV; Järvinen H; Kellokumpu I; Markie D; Neale K; Phillips R; Rozen P; Syngal S; Vijg J; Tomlinson IP; Aaltonen LA; Eng C
Cancer Res; 1997 Nov; 57(22):5017-21. PubMed ID: 9371495
[TBL] [Abstract][Full Text] [Related]
5. [Acral keratoses and inverted follicular keratosis presenting Cowden disease].
Larumbe A; Iglesias ME; Illarramendi JJ; Córdoba A; Gállego M
Actas Dermosifiliogr; 2007; 98(6):425-9. PubMed ID: 17663933
[TBL] [Abstract][Full Text] [Related]
6. Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinomas.
Marsh DJ; Zheng Z; Zedenius J; Kremer H; Padberg GW; Larsson C; Longy M; Eng C
Cancer Res; 1997 Feb; 57(3):500-3. PubMed ID: 9012481
[TBL] [Abstract][Full Text] [Related]
7. Cowden syndrome (multiple hamartoma syndrome).
Mallory SB
Dermatol Clin; 1995 Jan; 13(1):27-31. PubMed ID: 7712647
[TBL] [Abstract][Full Text] [Related]
8. Association between Cowden syndrome and Lhermitte-Duclos disease: report of two cases and review of the literature.
Derrey S; Proust F; Debono B; Langlois O; Layet A; Layet V; Longy M; Fréger P; Laquerrière A
Surg Neurol; 2004 May; 61(5):447-54; discussion 454. PubMed ID: 15120218
[TBL] [Abstract][Full Text] [Related]
9. Lhermitte-Duclos type cerebellum hamartoma and Cowden disease.
Vital A; Vital C; Martin-Negrier ML; McGrogan G; Bioulac P; Trojani M; Loiseau H; Rougier A
Clin Neuropathol; 1994; 13(4):229-31. PubMed ID: 7955671
[TBL] [Abstract][Full Text] [Related]
10. Cowden syndrome.
Ravi Prakash SM; Suma GN; Goel S
Indian J Dent Res; 2010; 21(3):439-42. PubMed ID: 20930359
[TBL] [Abstract][Full Text] [Related]
11. Multiple colon carcinomas in a patient with Cowden syndrome.
Bosserhoff AK; Grussendorf-Conen EI; Rübben A; Rudnik-Schöneborn S; Zerres K; Buettner R; Merkelbach-Bruse S
Int J Mol Med; 2006 Oct; 18(4):643-7. PubMed ID: 16964417
[TBL] [Abstract][Full Text] [Related]
12. [Cowden syndrome: clinical case presentation with oral lesions].
Almenar Besó R; Vicente Bagán Sebastián J; Milián Masanet MA; Jiménez Soriano Y
An Med Interna; 2001 Aug; 18(8):426-8. PubMed ID: 11589081
[TBL] [Abstract][Full Text] [Related]
13. Mucocutaneous papillomatous papules in Cowden's syndrome.
Jornayvaz FR; Philippe J
Clin Exp Dermatol; 2008 Mar; 33(2):151-3. PubMed ID: 18021272
[TBL] [Abstract][Full Text] [Related]
14. Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.
Bowles KR; Gajarski R; Porter P; Goytia V; Bachinski L; Roberts R; Pignatelli R; Towbin JA
J Clin Invest; 1996 Sep; 98(6):1355-60. PubMed ID: 8823300
[TBL] [Abstract][Full Text] [Related]
15. [Cowden syndrome].
Petritsch W; Pristautz H; Schreiber F; Stauber R; Kullnig P; Höfler H; Smolle J
Z Gastroenterol; 1990 Jul; 28(7):358-62. PubMed ID: 2173290
[TBL] [Abstract][Full Text] [Related]
16. Cowden's syndrome with Lhermitte-Duclos disease.
Boonpipattanapong T; Phuenpathom N; Mitarnun W
Br J Neurosurg; 2005 Aug; 19(4):361-5. PubMed ID: 16455548
[TBL] [Abstract][Full Text] [Related]
17. Somatic deletions and mutations in the Cowden disease gene, PTEN, in sporadic thyroid tumors.
Dahia PL; Marsh DJ; Zheng Z; Zedenius J; Komminoth P; Frisk T; Wallin G; Parsons R; Longy M; Larsson C; Eng C
Cancer Res; 1997 Nov; 57(21):4710-3. PubMed ID: 9354427
[TBL] [Abstract][Full Text] [Related]
18. Familial ovarian carcinoma: pedigree studies and preliminary results from linkage analysis.
Sobol H; Mazoyer S; Smith SA; Lyonnet D; Bignon YJ; Narod SA; Ardoin A; Biron P; Bobin JY; Bremond A
Bull Cancer; 1993 Feb; 80(2):121-34. PubMed ID: 8173163
[TBL] [Abstract][Full Text] [Related]
19. Germline BRCA1 mutations and loss of the wild-type allele in tumors from families with early onset breast and ovarian cancer.
Merajver SD; Frank TS; Xu J; Pham TM; Calzone KA; Bennett-Baker P; Chamberlain J; Boyd J; Garber JE; Collins FS
Clin Cancer Res; 1995 May; 1(5):539-44. PubMed ID: 9816013
[TBL] [Abstract][Full Text] [Related]
20. Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regions.
Kerangueven F; Eisinger F; Noguchi T; Allione F; Wargniez V; Eng C; Padberg G; Theillet C; Jacquemier J; Longy M; Sobol H; Birnbaum D
Oncogene; 1997 Jan; 14(3):339-47. PubMed ID: 9018120
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]