Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 84

1.

Peutz-Jeghers Syndrome.

Riegert-Johnson D, Gleeson FC, Westra W, Hefferon T, Wong Kee Song LM, Spurck L, Boardman LA.

In: Riegert-Johnson DL, Boardman LA, Hefferon T, Roberts M, editors. Cancer Syndromes [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2009-.
2008 Jul 18 [updated 2008 Aug 09].

2.

Psychosocial impact of Peutz-Jeghers Syndrome.

Woo A, Sadana A, Mauger DT, Baker MJ, Berk T, McGarrity TJ.

Fam Cancer. 2009;8(1):59-65. doi: 10.1007/s10689-008-9202-z. Epub 2008 Jul 5.

PMID:
18604594
[PubMed - indexed for MEDLINE]
3.

Case studies in the diagnosis and management of Peutz-Jeghers syndrome.

Riegert-Johnson D, Roberts M, Gleeson FC, Krishna M, Boardman L.

Fam Cancer. 2011 Sep;10(3):463-8. doi: 10.1007/s10689-011-9438-x.

PMID:
21503748
[PubMed - indexed for MEDLINE]
4.

Extraintestinal polyps in Peutz-Jeghers syndrome: presentation of four cases and review of the literature. Deutsche Peutz-Jeghers-Studiengruppe.

Vogel T, Schumacher V, Saleh A, Trojan J, Möslein G.

Int J Colorectal Dis. 2000 Apr;15(2):118-23. Review.

PMID:
10855556
[PubMed - indexed for MEDLINE]
5.

Quality of life and psychological distress in patients with Peutz-Jeghers syndrome.

van Lier MG, Mathus-Vliegen EM, van Leerdam ME, Kuipers EJ, Looman CW, Wagner A, Vanheusden K.

Clin Genet. 2010 Sep;78(3):219-26. doi: 10.1111/j.1399-0004.2010.01469.x.

PMID:
20695872
[PubMed - indexed for MEDLINE]
6.

Genotype-phenotype correlations in Peutz-Jeghers syndrome.

Amos CI, Keitheri-Cheteri MB, Sabripour M, Wei C, McGarrity TJ, Seldin MF, Nations L, Lynch PM, Fidder HH, Friedman E, Frazier ML.

J Med Genet. 2004 May;41(5):327-33.

PMID:
15121768
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Solitary Peutz-Jeghers Polyp in a Paediatric Patient.

Retrosi G, Nanni L, Vecchio FM, Manzoni C, Canali R, Busato G, Pintus C.

Case Rep Gastroenterol. 2010 Oct 18;4(3):452-456.

PMID:
21103204
[PubMed]
Free PMC Article
8.

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.

PMID:
10398133
[PubMed - indexed for MEDLINE]
9.

Peutz-Jeghers syndrome: clinicopathology and molecular alterations.

McGarrity TJ, Amos C.

Cell Mol Life Sci. 2006 Sep;63(18):2135-44. Review.

PMID:
16952058
[PubMed - indexed for MEDLINE]
10.

[Clinical classification of Peutz-Jeghers syndrome].

Dai YC, Song YG, Xiao B, Zhang YL, Zhi FC, Jiang B, Zhou DY.

Nan Fang Yi Ke Da Xue Xue Bao. 2006 Jan;26(1):79-81. Chinese.

PMID:
16495182
[PubMed - indexed for MEDLINE]
Free Article
11.

Two novel STK11 mutations in three Chinese families with Peutz-Jeghers syndrome.

Zuo YG, Xu KJ, Su B, Ho MG, Liu YH.

Chin Med J (Engl). 2007 Jul 5;120(13):1183-6.

PMID:
17637250
[PubMed - indexed for MEDLINE]
12.

High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome.

van Lier MG, Westerman AM, Wagner A, Looman CW, Wilson JH, de Rooij FW, Lemmens VE, Kuipers EJ, Mathus-Vliegen EM, van Leerdam ME.

Gut. 2011 Feb;60(2):141-7. doi: 10.1136/gut.2010.223750.

PMID:
21205875
[PubMed - indexed for MEDLINE]
13.

[Clinical analysis of Peutz-Jeghers syndrome:a report of 6 cases].

Dong K, Li B, Li BH, Guan QL, Huo YZ.

Zhonghua Wei Chang Wai Ke Za Zhi. 2005 Jul;8(4):336-8. Chinese.

PMID:
16167257
[PubMed - indexed for MEDLINE]
14.

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.

PMID:
16287113
[PubMed - indexed for MEDLINE]
15.

Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity.

Mehenni H, Gehrig C, Nezu J, Oku A, Shimane M, Rossier C, Guex N, Blouin JL, Scott HS, Antonarakis SE.

Am J Hum Genet. 1998 Dec;63(6):1641-50.

PMID:
9837816
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Peutz-Jeghers syndrome: risks of a hereditary condition.

Westerman AM, Wilson JH.

Scand J Gastroenterol Suppl. 1999;230:64-70. Review.

PMID:
10499464
[PubMed - indexed for MEDLINE]
17.

A De Novo mutation of STK11 gene in a Chinese patient with Peutz-Jeghers syndrome.

Gao Y, Zhang FM, Huang S, Wang X, Zhang P, Huang XD, Ji GZ, Fan ZN.

Dig Dis Sci. 2010 Apr;55(4):1032-6. doi: 10.1007/s10620-009-0837-x. Epub 2009 Jun 9.

PMID:
19507030
[PubMed - indexed for MEDLINE]
18.

A novel de novo mutation in LKB1 gene in a Chinese Peutz Jeghers syndrome patient significantly diminished p53 activity.

Liu L, Du X, Nie J.

Clin Res Hepatol Gastroenterol. 2011 Mar;35(3):221-6. doi: 10.1016/j.clinre.2010.11.008. Epub 2011 Mar 15.

PMID:
21411391
[PubMed - indexed for MEDLINE]
19.

One novel deletion and one splicing mutation of the LKB1 gene in two Chinese patients with Peutz-Jeghers syndrome.

Chen C, Zhang X, Wang F, Liu C, Lu H, Wan H, Wei J, Liu J.

DNA Cell Biol. 2012 Oct;31(10):1535-40. Epub 2012 Aug 28.

PMID:
22928647
[PubMed - indexed for MEDLINE]
20.

Elevation of WNT5A expression in polyp formation in Lkb1+/- mice and Peutz-Jeghers syndrome.

Lai C, Robinson J, Clark S, Stamp G, Poulsom R, Silver A.

J Pathol. 2011 Apr;223(5):584-92. doi: 10.1002/path.2835. Epub 2011 Feb 21.

PMID:
21341271
[PubMed - indexed for MEDLINE]
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk