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Results: 1 to 20 of 310

Similar articles for PubMed (Select 15617552)

1.

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.

PMID:
15617552
2.

A novel mutation in the FERMT1 gene in Turkish siblings with Kindler syndrome.

Kartal D, Borlu M, Has C, Fölster-Holst R.

J Eur Acad Dermatol Venereol. 2015 Apr 10. doi: 10.1111/jdv.13163. [Epub ahead of print] No abstract available.

PMID:
25865288
3.

Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz-Jeghers syndrome.

Borun P, De Rosa M, Nedoszytko B, Walkowiak J, Plawski A.

Fam Cancer. 2015 Apr 5. [Epub ahead of print]

PMID:
25841653
4.

Emergency medicine. Lee v. Hennepin County, Civil No. 13-1328 PJS/AJB (D. Minn. November 20, 2013).

West JC.

J Healthc Risk Manag. 2015;34(3):43-4. No abstract available.

PMID:
25796634
5.

A single-nucleotide polymorphism in serine-threonine kinase 11, the gene encoding liver kinase B1, is a risk factor for multiple sclerosis.

Boullerne AI, Skias D, Hartman EM, Testai FD, Kalinin S, Polak PE, Feinstein DL.

ASN Neuro. 2015 Feb 18;7(1). pii: 1759091415568914. doi: 10.1177/1759091415568914. Print 2015 Jan-Feb.

6.

High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case report.

Noriega-Iriondo MF, Colon-Otero G, Kipp BR, Copland JA, Ferber MJ, Marlow LA, Roberts ME, Robertson MW, Dinh TA, Attia S, Geiger XJ, Riegert-Johnson DL.

Hered Cancer Clin Pract. 2015 Jan 23;13(1):6. doi: 10.1186/s13053-015-0027-0. eCollection 2015.

7.

Microdeletion of 19p13.3 in a girl with Peutz-Jeghers syndrome, intellectual disability, hypotonia, and distinctive features.

Kuroda Y, Saito T, Nagai J, Ida K, Naruto T, Masuno M, Kurosawa K.

Am J Med Genet A. 2015 Feb;167A(2):389-93. doi: 10.1002/ajmg.a.36813. Epub 2014 Dec 8.

PMID:
25487640
8.

Gastric cancer in three relatives of a patient with a biallelic IL12RB1 mutation.

Vogelaar IP, van der Post RS, van de Vosse E, van Krieken JH, Hoogerbrugge N, Ligtenberg MJ, Gómez García E.

Fam Cancer. 2015 Mar;14(1):89-94. doi: 10.1007/s10689-014-9764-x.

PMID:
25467645
9.

Presymptomatic identification of CDH1 germline mutation in a healthy korean individual with family history of gastric cancer.

Choi HJ, Ki CS, Suh SP, Kim JW.

Ann Lab Med. 2014 Sep;34(5):386-9. doi: 10.3343/alm.2014.34.5.386. Epub 2014 Aug 21.

10.

[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. doi: 10.1684/bdc.2014.1942. Review. French.

PMID:
25036236
11.

Peutz-Jeghers syndrome with germline mutation of STK11.

Chae HD, Jeon CH.

Ann Surg Treat Res. 2014 Jun;86(6):325-30. doi: 10.4174/astr.2014.86.6.325. Epub 2014 May 23.

12.

[Mutation analysis of STK11 gene in a Chinese family with Peutz-Jeghers syndrome].

Zhao X, Huang Y, Yang B, Zhao Y.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Jun;31(3):294-7. doi: 10.3760/cma.j.issn.1003-9406.2014.03.008. Chinese.

PMID:
24928005
13.

Umbilical pigmentation in Peutz-Jeghers syndrome.

Morrison PT, Donnelly DE, Morrison PJ.

Clin Dysmorphol. 2014 Jul;23(3):114-5. doi: 10.1097/MCD.0000000000000044. No abstract available.

PMID:
24878829
14.

STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome.

Wang Z, Wu B, Mosig RA, Chen Y, Ye F, Zhang Y, Gong W, Gong L, Huang F, Wang X, Nie B, Zheng H, Cui M, Wang Y, Wang J, Chen C, Polydorides AD, Zhang DY, Martignetti JA, Jiang B.

Hum Mutat. 2014 Jul;35(7):851-8. doi: 10.1002/humu.22549. Epub 2014 Jun 3.

PMID:
24652667
15.

A new family with a germline ANKRD26 mutation and predisposition to myeloid malignancies.

Marquez R, Hantel A, Lorenz R, Neistadt B, Wong J, Churpek JE, Mardini NA, Shaukat I, Gurbuxani S, Miller JL, Godley LA.

Leuk Lymphoma. 2014 Dec;55(12):2945-6. doi: 10.3109/10428194.2014.903476. Epub 2014 Apr 22. No abstract available.

16.

Novel and recurrent mutations of STK11 gene in six Chinese cases with Peutz-Jeghers syndrome.

Dai L, Fu L, Liu D, Zhang K, Wu Y, Meng H, Zhang B, Guan X, Guo H, Bai Y.

Dig Dis Sci. 2014 Aug;59(8):1856-61. doi: 10.1007/s10620-014-3077-7. Epub 2014 Mar 7.

PMID:
24604241
17.

A tumor of the uterine cervix with a complex histology in a Peutz-Jeghers syndrome patient with genomic deletion of the STK11 exon 1 region.

Kobayashi Y, Masuda K, Kimura T, Nomura H, Hirasawa A, Banno K, Susumu N, Sugano K, Aoki D.

Future Oncol. 2014 Feb;10(2):171-7. doi: 10.2217/fon.13.180.

PMID:
24490603
18.

A case of synchronous mucinous metaplasia and neoplasia of the female genital tract without an STK11 or KRAS mutation.

Nagahama K, Yamanaka S, Nakayama T, Tokinaga A, Asai-Sato M, Miyagi E, Tanaka R, Furuya M.

Gynecol Oncol Case Rep. 2013 Feb 18;5:4-5. doi: 10.1016/j.gynor.2013.02.005. eCollection 2013.

19.

Findings from the Peutz-Jeghers syndrome registry of uruguay.

Tchekmedyian A, Amos CI, Bale SJ, Zhu D, Arold S, Berrueta J, Nabon N, McGarrity T.

PLoS One. 2013 Nov 19;8(11):e79639. doi: 10.1371/journal.pone.0079639. eCollection 2013.

20.

Identification and characterization of CDH1 germline variants in sporadic gastric cancer patients and in individuals at risk of gastric cancer.

Garziera M, Canzonieri V, Cannizzaro R, Geremia S, Caggiari L, De Zorzi M, Maiero S, Orzes E, Perin T, Zanussi S, De Paoli P, De Re V.

PLoS One. 2013 Oct 29;8(10):e77035. doi: 10.1371/journal.pone.0077035. eCollection 2013.

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