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Items: 1 to 20 of 649

1.

A novel germline mutation (c.A527G) in STK11 gene causes Peutz-Jeghers syndrome in a Chinese girl: A case report.

Zhao ZY, Jiang YL, Li BR, Yang F, Li J, Jin XW, Sun SH, Ning SB.

Medicine (Baltimore). 2017 Dec;96(49):e8591. doi: 10.1097/MD.0000000000008591.

2.

A giant and extensive solitary Peutz-Jeghers-type polyp in the antrum of stomach: Case report.

Zou BC, Wang FF, Zhao G, Lu XL, Zhang L, Zhao P, Shi HT, Qin B, Guo XD, Zhang J.

Medicine (Baltimore). 2017 Dec;96(49):e8466. doi: 10.1097/MD.0000000000008466.

3.
4.

Spectrum of orocutaneous disease associations: Genodermatoses and inflammatory conditions.

Wilder EG, Frieder J, Sulhan S, Michel P, Cizenski JD, Wright JM, Menter MA.

J Am Acad Dermatol. 2017 Nov;77(5):809-830. doi: 10.1016/j.jaad.2017.02.017. Review.

PMID:
29029902
5.

A 23-Nucleotide Deletion in STK11 Gene Causes Peutz-Jeghers Syndrome and Malignancy in a Chinese Patient Without a Positive Family History.

Zhao ZY, Jiang YL, Li BR, Yang F, Li J, Jin XW, Ning SB, Sun SH.

Dig Dis Sci. 2017 Nov;62(11):3014-3020. doi: 10.1007/s10620-017-4741-5. Epub 2017 Oct 6.

PMID:
28986664
6.

Cancer risk in patients with Peutz-Jeghers syndrome: A retrospective cohort study of 336 cases.

Chen HY, Jin XW, Li BR, Zhu M, Li J, Mao GP, Zhang YF, Ning SB.

Tumour Biol. 2017 Jun;39(6):1010428317705131. doi: 10.1177/1010428317705131.

PMID:
28653895
7.

Pancreatic Adenocarcinoma: Improving Prevention and Survivorship.

Sohal DPS, Willingham FF, Falconi M, Raphael KL, Crippa S.

Am Soc Clin Oncol Educ Book. 2017;37:301-310. doi: 10.14694/EDBK_175222. Review.

8.

Genetic and epigenetic profiling of a solitary Peutz-Jeghers colon polyp.

Linhart H, Bormann F, Hutter B, Brors B, Lyko F.

Cold Spring Harb Mol Case Stud. 2017 May;3(3):a001610. doi: 10.1101/mcs.a001610.

9.

Peutz-Jeghers syndrome with intermittent upper intestinal obstruction: A case report and review of the literature.

Duan SX, Wang GH, Zhong J, Ou WH, Fu MX, Wang FS, Ma SH, Li JH.

Medicine (Baltimore). 2017 Apr;96(17):e6538. doi: 10.1097/MD.0000000000006538. Review.

10.

Current and future role of genetic screening in gynecologic malignancies.

Ring KL, Garcia C, Thomas MH, Modesitt SC.

Am J Obstet Gynecol. 2017 Nov;217(5):512-521. doi: 10.1016/j.ajog.2017.04.011. Epub 2017 Apr 12. Review.

PMID:
28411145
11.

Unusual ultrasound appearance of small bowel intussusception and secondary bowel obstruction in a child with Peutz-Jeghers syndrome.

Wu L, Iyer RS, Drugas GT, Stanescu AL.

Clin Imaging. 2017 May - Jun;43:136-139. doi: 10.1016/j.clinimag.2017.03.006. Epub 2017 Mar 9.

PMID:
28314199
12.

Familial pancreatic cancer: Concept, management and issues.

Matsubayashi H, Takaori K, Morizane C, Maguchi H, Mizuma M, Takahashi H, Wada K, Hosoi H, Yachida S, Suzuki M, Usui R, Furukawa T, Furuse J, Sato T, Ueno M, Kiyozumi Y, Hijioka S, Mizuno N, Terashima T, Mizumoto M, Kodama Y, Torishima M, Kawaguchi T, Ashida R, Kitano M, Hanada K, Furukawa M, Kawabe K, Majima Y, Shimosegawa T.

World J Gastroenterol. 2017 Feb 14;23(6):935-948. doi: 10.3748/wjg.v23.i6.935. Review.

13.

A novel mutation in the STK11 gene causes heritable Peutz-Jeghers syndrome - a case report.

Chen JH, Zheng JJ, Guo Q, Liu C, Luo B, Tang SB, Cheng JD, Huang EW.

BMC Med Genet. 2017 Feb 23;18(1):19. doi: 10.1186/s12881-017-0373-z.

14.

An update on small bowel endoscopy.

Ching HL, McAlindon ME, Sidhu R.

Curr Opin Gastroenterol. 2017 May;33(3):181-188. doi: 10.1097/MOG.0000000000000346. Review.

PMID:
28212152
15.

Lentiginous phenotypes caused by diverse pathogenic genes (SASH1 and PTPN11): clinical and molecular discrimination.

Zhang J, Cheng R, Liang J, Ni C, Li M, Yao Z.

Clin Genet. 2016 Oct;90(4):372-7. doi: 10.1111/cge.12728. Epub 2016 Feb 3.

PMID:
27659786
16.

Juvenile polyposis syndrome: An unusual case report of anemia and gastrointestinal bleeding in young infant.

Hsiao YH, Wei CH, Chang SW, Chang L, Fu YW, Lee HC, Liu HL, Yeung CY.

Medicine (Baltimore). 2016 Sep;95(37):e4550. doi: 10.1097/MD.0000000000004550.

17.

Heritable Gastrointestinal Cancer Syndromes.

Stoffel EM.

Gastroenterol Clin North Am. 2016 Sep;45(3):509-27. doi: 10.1016/j.gtc.2016.04.008. Review.

PMID:
27546846
18.

Hamartomatous polyps - a clinical and molecular genetic study.

Jelsig AM.

Dan Med J. 2016 Aug;63(8). pii: B5280. Review.

PMID:
27477802
19.

A Clinical and Molecular Genetic Study in 11 Chinese Children With Peutz-Jeghers Syndrome.

Zheng B, Wang C, Jia Z, Liu Z, Li M, Jin Y, Pan J.

J Pediatr Gastroenterol Nutr. 2017 Apr;64(4):559-564. doi: 10.1097/MPG.0000000000001316.

PMID:
27467201
20.

Giant rectal polyp prolapse in an adult patient with the Peutz-Jeghers syndrome.

Cano-Contreras AD, Meixueiro-Daza A, Grube-Pagola P, Remes-Troche JM.

BMJ Case Rep. 2016 Jul 21;2016. pii: bcr2016215629. doi: 10.1136/bcr-2016-215629.

PMID:
27444139

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