138 related articles for article (PubMed ID: 15067177)
1. Abnormal distribution and hyperplasia of thyroid C-cells in PTEN-associated tumor syndromes.
Zambrano E; Holm I; Glickman J; Huang S; Perez-Atayde A; Kozakewich HP; Shamberger RC; Nosé V
Endocr Pathol; 2004; 15(1):55-64. PubMed ID: 15067177
[TBL] [Abstract][Full Text] [Related]
2. Thyroid pathology in PTEN-hamartoma tumor syndrome: characteristic findings of a distinct entity.
Laury AR; Bongiovanni M; Tille JC; Kozakewich H; Nosé V
Thyroid; 2011 Feb; 21(2):135-44. PubMed ID: 21190448
[TBL] [Abstract][Full Text] [Related]
3. Thyroid Follicular Cell-derived Carcinomas in a Background of Multiple Adenomatous Nodules Leading to a Diagnosis of
Liu A; Borges PM; Tay YS; Thompson LDR; Kong MX; Lai J
Anticancer Res; 2022 Mar; 42(3):1481-1485. PubMed ID: 35220242
[TBL] [Abstract][Full Text] [Related]
4. Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway.
Zhou XP; Waite KA; Pilarski R; Hampel H; Fernandez MJ; Bos C; Dasouki M; Feldman GL; Greenberg LA; Ivanovich J; Matloff E; Patterson A; Pierpont ME; Russo D; Nassif NT; Eng C
Am J Hum Genet; 2003 Aug; 73(2):404-11. PubMed ID: 12844284
[TBL] [Abstract][Full Text] [Related]
5. Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases.
Hendriks YM; Verhallen JT; van der Smagt JJ; Kant SG; Hilhorst Y; Hoefsloot L; Hansson KB; van der Straaten PJ; Boutkan H; Breuning MH; Vasen HF; Bröcker-Vriends AH
Fam Cancer; 2003; 2(2):79-85. PubMed ID: 14574156
[TBL] [Abstract][Full Text] [Related]
6. The role of PTEN, a phosphatase gene, in inherited and sporadic nonmedullary thyroid tumors.
Eng C
Recent Prog Horm Res; 1999; 54():441-52; discussion 453. PubMed ID: 10548886
[TBL] [Abstract][Full Text] [Related]
7. Role of PTEN, a lipid phosphatase upstream effector of protein kinase B, in epithelial thyroid carcinogenesis.
Eng C
Ann N Y Acad Sci; 2002 Jun; 968():213-21. PubMed ID: 12119278
[TBL] [Abstract][Full Text] [Related]
8. Germline mutations in the PTEN gene in Israeli patients with Bannayan-Riley-Ruvalcaba syndrome and women with familial breast cancer.
Figer A; Kaplan A; Frydman M; Lev D; Paswell J; Papa MZ; Goldman B; Friedman E
Clin Genet; 2002 Oct; 62(4):298-302. PubMed ID: 12372056
[TBL] [Abstract][Full Text] [Related]
9. PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.
Marsh DJ; Kum JB; Lunetta KL; Bennett MJ; Gorlin RJ; Ahmed SF; Bodurtha J; Crowe C; Curtis MA; Dasouki M; Dunn T; Feit H; Geraghty MT; Graham JM; Hodgson SV; Hunter A; Korf BR; Manchester D; Miesfeldt S; Murday VA; Nathanson KL; Parisi M; Pober B; Romano C; Eng C
Hum Mol Genet; 1999 Aug; 8(8):1461-72. PubMed ID: 10400993
[TBL] [Abstract][Full Text] [Related]
10. Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation.
Marsh DJ; Coulon V; Lunetta KL; Rocca-Serra P; Dahia PL; Zheng Z; Liaw D; Caron S; Duboué B; Lin AY; Richardson AL; Bonnetblanc JM; Bressieux JM; Cabarrot-Moreau A; Chompret A; Demange L; Eeles RA; Yahanda AM; Fearon ER; Fricker JP; Gorlin RJ; Hodgson SV; Huson S; Lacombe D; Eng C
Hum Mol Genet; 1998 Mar; 7(3):507-15. PubMed ID: 9467011
[TBL] [Abstract][Full Text] [Related]
11. PTEN: one gene, many syndromes.
Eng C
Hum Mutat; 2003 Sep; 22(3):183-98. PubMed ID: 12938083
[TBL] [Abstract][Full Text] [Related]
12. Germline PTEN mutation in a family with Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome.
Zori RT; Marsh DJ; Graham GE; Marliss EB; Eng C
Am J Med Genet; 1998 Dec; 80(4):399-402. PubMed ID: 9856571
[TBL] [Abstract][Full Text] [Related]
13. Thyroid Pathology Findings in Cowden Syndrome: A Clue for the Diagnosis of the PTEN Hamartoma Tumor Syndrome.
Cameselle-Teijeiro J; Fachal C; Cabezas-Agrícola JM; Alfonsín-Barreiro N; Abdulkader I; Vega-Gliemmo A; Hermo JA
Am J Clin Pathol; 2015 Aug; 144(2):322-8. PubMed ID: 26185318
[TBL] [Abstract][Full Text] [Related]
14. Constipation, polyps, or cancer? Let PTEN predict your future.
Eng C
Am J Med Genet A; 2003 Nov; 122A(4):315-22. PubMed ID: 14518069
[TBL] [Abstract][Full Text] [Related]
15. Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype.
Longy M; Coulon V; Duboué B; David A; Larrègue M; Eng C; Amati P; Kraimps JL; Bottani A; Lacombe D; Bonneau D
J Med Genet; 1998 Nov; 35(11):886-9. PubMed ID: 9832032
[TBL] [Abstract][Full Text] [Related]
16. Thyroid pathologic findings in patients with Cowden disease.
Harach HR; Soubeyran I; Brown A; Bonneau D; Longy M
Ann Diagn Pathol; 1999 Dec; 3(6):331-40. PubMed ID: 10594284
[TBL] [Abstract][Full Text] [Related]
17. Absence of germline mutations in MINPP1, a phosphatase encoding gene centromeric of PTEN, in patients with Cowden and Bannayan-Riley-Ruvalcaba syndrome without germline PTEN mutations.
Dahia PM; Gimm O; Chi H; Marsh DJ; Reynolds PR; Eng C
J Med Genet; 2000 Sep; 37(9):715-7. PubMed ID: 11182934
[No Abstract] [Full Text] [Related]
18. Papillary carcinoma occurring within an adenomatous goiter of the thyroid gland in Cowden's disease.
Kameyama K; Takami H; Miyajima K; Mimura T; Hosoda Y; Ito K; Ito K
Endocr Pathol; 2001; 12(1):73-6. PubMed ID: 11478271
[TBL] [Abstract][Full Text] [Related]
19. Thyroid involvement in two patients with Bannayan-Riley-Ruvalcaba syndrome.
Peiretti V; Mussa A; Feyles F; Tuli G; Santanera A; Molinatto C; Ferrero GB; Corrias A
J Clin Res Pediatr Endocrinol; 2013; 5(4):261-5. PubMed ID: 24379037
[TBL] [Abstract][Full Text] [Related]
20. Genital lentigines in a 6-year-old boy with a family history of Cowden's disease: clinical and genetic evidence of the linkage between Bannayan-Riley-Ruvacalba syndrome and Cowden's disease.
Blum RR; Rahimizadeh A; Kardon N; Lebwohl M; Wei H
J Cutan Med Surg; 2001; 5(3):228-30. PubMed ID: 11685670
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
