201 related articles for article (PubMed ID: 20310004)
1. Sertoli Leydig cell ovarian tumour and gastric polyps as presenting features of Peutz-Jeghers syndrome.
Howell L; Bader A; Mullassery D; Losty P; Auth M; Kokai G
Pediatr Blood Cancer; 2010 Jul; 55(1):206-7. PubMed ID: 20310004
[TBL] [Abstract][Full Text] [Related]
2. Sertoli cell tumor causing precocious puberty in a girl with Peutz-Jeghers syndrome.
Zung A; Shoham Z; Open M; Altman Y; Dgani R; Zadik Z
Gynecol Oncol; 1998 Sep; 70(3):421-4. PubMed ID: 9790799
[TBL] [Abstract][Full Text] [Related]
3. [Gastric adenocarcinoma in hamartomatous polyp in Peutz-Jeghers syndrome].
Bujanda L; Beguiristain A; Villar JM; Cosme A; Castiella A; Arriola JA; Arenas JI
Gastroenterol Hepatol; 1996 Nov; 19(9):452-5. PubMed ID: 8998668
[TBL] [Abstract][Full Text] [Related]
4. Gastric outlet obstruction in a neonate because of Peutz-Jeghers syndrome.
Burgmeier C; Schier F; Staatz G
J Pediatr Surg; 2012 Aug; 47(8):e1-3. PubMed ID: 22901935
[TBL] [Abstract][Full Text] [Related]
5. A novel STK11 germline mutation in two siblings with Peutz-Jeghers syndrome complicated by primary gastric cancer.
Shinmura K; Goto M; Tao H; Shimizu S; Otsuki Y; Kobayashi H; Ushida S; Suzuki K; Tsuneyoshi T; Sugimura H
Clin Genet; 2005 Jan; 67(1):81-6. PubMed ID: 15617552
[TBL] [Abstract][Full Text] [Related]
6. An unusual case of sex cord tumor with annular tubules with malignant transformation in a patient with Peutz-Jeghers syndrome.
Barker D; Sharma R; McIndoe A; Blair E; Hall M; Gabra H; El-Bahrawy M
Int J Gynecol Pathol; 2010 Jan; 29(1):27-32. PubMed ID: 19952941
[TBL] [Abstract][Full Text] [Related]
7. Complete germline deletion of the STK11 gene in a family with Peutz-Jeghers syndrome.
Le Meur N; Martin C; Saugier-Veber P; Joly G; Lemoine F; Moirot H; Rossi A; Bachy B; Cabot A; Joly P; Frébourg T
Eur J Hum Genet; 2004 May; 12(5):415-8. PubMed ID: 14970844
[TBL] [Abstract][Full Text] [Related]
8. High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
Aretz S; Stienen D; Uhlhaas S; Loff S; Back W; Pagenstecher C; McLeod DR; Graham GE; Mangold E; Santer R; Propping P; Friedl W
Hum Mutat; 2005 Dec; 26(6):513-9. PubMed ID: 16287113
[TBL] [Abstract][Full Text] [Related]
9. A novel germline mutation of the LKB1 gene in a patient with Peutz-Jeghers syndrome with early-onset gastric cancer.
Takahashi M; Sakayori M; Takahashi S; Kato T; Kaji M; Kawahara M; Suzuki T; Kato S; Kato S; Shibata H; Murakawa Y; Yoshioka T; Ishioka C
J Gastroenterol; 2004 Dec; 39(12):1210-4. PubMed ID: 15622488
[TBL] [Abstract][Full Text] [Related]
10. Somatic mutations of LKB1 and beta-catenin genes in gastrointestinal polyps from patients with Peutz-Jeghers syndrome.
Miyaki M; Iijima T; Hosono K; Ishii R; Yasuno M; Mori T; Toi M; Hishima T; Shitara N; Tamura K; Utsunomiya J; Kobayashi N; Kuroki T; Iwama T
Cancer Res; 2000 Nov; 60(22):6311-3. PubMed ID: 11103790
[TBL] [Abstract][Full Text] [Related]
11. Morphologic characterization of syndromic gastric polyps.
Lam-Himlin D; Park JY; Cornish TC; Shi C; Montgomery E
Am J Surg Pathol; 2010 Nov; 34(11):1656-62. PubMed ID: 20924281
[TBL] [Abstract][Full Text] [Related]
12. Mapping of a translocation breakpoint in a Peutz-Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11-negative PJS cases.
Hearle N; Lucassen A; Wang R; Lim W; Ross F; Wheeler R; Moore I; Shipley J; Houlston R
Genes Chromosomes Cancer; 2004 Oct; 41(2):163-9. PubMed ID: 15287029
[TBL] [Abstract][Full Text] [Related]
13. Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. Online.
Kruse R; Uhlhaas S; Lamberti C; Keller KM; Jackisch C; Steinhard J; Knöpfle G; Loff S; Back W; Stolte M; Jungck M; Propping P; Friedl W; Jenne DE
Hum Mutat; 1999; 13(3):257-8. PubMed ID: 10090485
[TBL] [Abstract][Full Text] [Related]
14. Carcinoma in situ arising in a gastric hamartomatous polyp in a patient with Peutz-Jeghers syndrome.
Defago MR; Higa AL; Campra JL; Paradelo M; Uehara A; Torres Mazzucchi MH; Videla R
Endoscopy; 1996 Feb; 28(2):267. PubMed ID: 8739752
[No Abstract] [Full Text] [Related]
15. STK11/LKB1 germline mutations in the first Peutz-Jeghers syndrome patients identified in Slovakia.
Bartosova Z; Zavodna K; Krivulcik T; Usak J; Mlkva I; Kruzliak T; Hromec J; Usakova V; Kopecka I; Veres P; Bartosova Z; Bujalkova M
Neoplasma; 2007; 54(2):101-7. PubMed ID: 17319781
[TBL] [Abstract][Full Text] [Related]
16. The usefulness of intra-operative endoscopy in Peutz-Jeghers syndrome: a case report.
Yagmurdur MC; Daphan C; Ozdemir A; Ozenc A; Bayraktar Y; Uzunalimoglu B
Hepatogastroenterology; 1998; 45(24):2175-8. PubMed ID: 9951888
[TBL] [Abstract][Full Text] [Related]
17. Different phenotypes including gynecological cancer in three female patients with Peutz-Jeghers syndrome and mutations in the STK11 gene.
Heinritz W; Strenge S; Kujat A; Hockel M; Froster UG
Onkologie; 2008 Nov; 31(11):625-8. PubMed ID: 19145097
[TBL] [Abstract][Full Text] [Related]
18. De novo germline mutation in the serine-threonine kinase STK11/LKB1 gene associated with Peutz-Jeghers syndrome.
Hernan I; Roig I; Martin B; Gamundi MJ; Martinez-Gimeno M; Carballo M
Clin Genet; 2004 Jul; 66(1):58-62. PubMed ID: 15200509
[TBL] [Abstract][Full Text] [Related]
19. Allelic imbalance at the LKB1 (STK11) locus in tumours from patients with Peutz-Jeghers' syndrome provides evidence for a hamartoma-(adenoma)-carcinoma sequence.
Wang ZJ; Ellis I; Zauber P; Iwama T; Marchese C; Talbot I; Xue WH; Yan ZY; Tomlinson I
J Pathol; 1999 May; 188(1):9-13. PubMed ID: 10398133
[TBL] [Abstract][Full Text] [Related]
20. [Hereditary predisposition to cancers of the digestive tract, breast, gynecological and gonadal: focus on the Peutz-Jeghers].
Turpin A; Cattan S; Leclerc J; Wacrenier A; Manouvrier-Hanu S; Buisine MP; Lejeune-Dumoulin S
Bull Cancer; 2014 Sep; 101(9):813-22. PubMed ID: 25036236
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]