High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome.
about
Hamartomatous polyposis syndromes: a reviewMolecular approach to genetic and epigenetic pathogenesis of early-onset colorectal cancerUpdate on imaging of Peutz-Jeghers syndromeColorectal cancer risk in hamartomatous polyposis syndromesHigh risk factors of pancreatic carcinoma.Management of precancerous conditions and lesions in the stomach (MAPS): guideline from the European Society of Gastrointestinal Endoscopy (ESGE), European Helicobacter Study Group (EHSG), European Society of Pathology (ESP), and the Sociedade PortuOrgan-sparing surgery of the bilateral testicular large cell calcifying sertoli cell tumor in patient with atypical Peutz-Jeghers syndrome.Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers.Multiple genital tract tumors and mucinous adenocarcinoma of colon in a woman with Peutz-Jeghers syndrome: a case report and review of literaturesA novel mutation in STK11 gene is associated with Peutz-Jeghers syndrome in Chinese patients.Familial colon cancer syndromes: an update of a rapidly evolving fieldFindings from the Peutz-Jeghers syndrome registry of uruguay.A novel mutation in the STK11 gene causes heritable Peutz-Jeghers syndrome - a case reportPeutz-Jeghers Syndrome With Diffuse Gastrointestinal Polyposis: Three Cases in a Family With Different Manifestations and No Evidence of Malignancy During 14 Years Follow UpFamilial gastric cancer: detection of a hereditary cause helps to understand its etiology.Syndrome-Associated Tumors by Organ System.Reduced life expectancy seen in hereditary diseases which predispose to early-onset tumors.Genetic Screening and Analysis of LKB1 Gene in Chinese Patients with Peutz-Jeghers Syndrome.Pathology and Genetics of Syndromic Gastric Polyps.Histopathological, Molecular, and Genetic Profile of Hereditary Diffuse Gastric Cancer: Current Knowledge and Challenges for the Future.Syndromic Gastric Polyps: At the Crossroads of Genetic and Environmental Cancer Predisposition.Time to incorporate germline multigene panel testing into breast and ovarian cancer patient care.LKB1 when associated with methylatedERα is a marker of bad prognosis in breast cancer.Hereditary syndromes predisposing to endocrine tumors and their skin manifestations.STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome.Cancer risk in patients with Peutz-Jeghers syndrome: A retrospective cohort study of 336 cases.Acute intussusception and polyp with malignant transformation in Peutz-Jeghers syndrome: A case report.Appendix carcinoid associated with the Peutz-Jeghers syndrome.Clinical presentations and surgical approach of acute intussusception caused by Peutz-Jeghers syndrome in adults.Identification of molecular alterations in gastrointestinal carcinomas and dysplastic hamartomas in Peutz-Jeghers syndrome.Sanger sequencing in exonic regions of STK11 gene uncovers a novel de-novo germline mutation (c.962_963delCC) associated with Peutz-Jeghers syndrome and elevated cancer risk: case report of a Chinese patient.Large deletions and splicing-site mutations in the STK11 gene in Peutz-Jeghers Chilean families.A 23-Nucleotide Deletion in STK11 Gene Causes Peutz-Jeghers Syndrome and Malignancy in a Chinese Patient Without a Positive Family History.An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review.Gastrointestinal diseases and their oro-dental manifestations: Part 4: Peutz-Jeghers syndrome.Peutz -Jeghers syndrome (PJS).A Peutz-Jeghers syndrome family associated with sinonasal adenocarcinoma: 28 years follow up report.Two novel STK11 missense mutations induce phosphorylation of S6K and promote cell proliferation in Peutz-Jeghers syndrome.Colorectal polyposis and inherited colorectal cancer syndromes.Close and regular surveillance is key to prevent severe complications for Peutz-Jeghers syndrome patients without gastrointestinal polyps: case report of a novel STK11 mutation (c.471_472delCT) in a Chinese girl.
P2860
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P2860
High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome.
description
2011 nî lūn-bûn
@nan
2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome.
@ast
High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome.
@en
High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome.
@nl
type
label
High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome.
@ast
High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome.
@en
High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome.
@nl
prefLabel
High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome.
@ast
High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome.
@en
High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome.
@nl
P2093
P356
P1433
P1476
High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome.
@en
P2093
Anja Wagner
Anne Marie Westerman
Caspar W N Looman
Elisabeth M H Mathus-Vliegen
Felix W M de Rooij
J H Paul Wilson
Margot G F van Lier
Monique E van Leerdam
Valery E P P Lemmens
P304
P356
10.1136/GUT.2010.223750
P407
P577
2011-02-01T00:00:00Z