about
Distinct gene expression signatures in lynch syndrome and familial colorectal cancer type x.Functional examination of MLH1, MSH2, and MSH6 intronic mutations identified in Danish colorectal cancer patients.Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome.Surveillance for urinary tract cancer in Lynch syndrome.Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome population.A proposed staging system and stage-specific interventions for familial adenomatous polyposisOutcome of 24 years national surveillance in different hereditary colorectal cancer subgroups leading to more individualised surveillance.Deranged Wnt signaling is frequent in hereditary nonpolyposis colorectal cancer.Risk of gynecologic cancers in Danish hereditary non-polyposis colorectal cancer families.Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database.Barrett's esophagus and esophageal adenocarcinoma. Endoscopic and histologic surveillance.Differential expression of CK20, β-catenin, and MUC2/5AC/6 in Lynch syndrome and familial colorectal cancer type XThe effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers.Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk.Functional characterization of MLH1 missense variants identified in Lynch syndrome patients.Interobserver variability in the evaluation of mismatch repair protein immunostaining.Gain of chromosomal region 20q and loss of 18 discriminates between Lynch syndrome and familial colorectal cancer.Recommendations to improve identification of hereditary and familial colorectal cancer in Europe.[Prevention of colorectal cancer in families with hereditary nonpolyposis colorectal cancer].Survival of patients with Stage III colon cancer is improved in hereditary non-polyposis colorectal cancer compared with sporadic cases. A Danish registry based study.Limited impact on self-concept in individuals with Lynch syndrome; results from a national cohort study.Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patients.Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutation.Validation of a self-concept scale for Lynch syndrome in different nationalities.Mismatch repair defective breast cancer in the hereditary nonpolyposis colorectal cancer syndrome.Iatrogenic psoas abscess. Case report.HNPCC-associated synchronous early-stage signet-ring cell carcinomas of colonic origin. A comparative morphological and immunohistochemical study of an intramucosal and a submucosal example.[Serrated, hyperplastic and hyperplasia-like colorectal polyps].The clinical features of ovarian cancer in hereditary nonpolyposis colorectal cancer.Sessile serrated polyps of the colorectum are rare in patients with Lynch syndrome and in familial colorectal cancer families.Hereditary colorectal cancer diagnostics: morphological features of familial colorectal cancer type X versus Lynch syndrome.Mandibular osteomas in sporadic colorectal carcinoma. A genetic marker.Cancer Risks for PMS2-Associated Lynch SyndromeRisk of multiple colorectal cancer development depends on age and subgroup in individuals with hereditary predispositionMSH6 Mutations are Frequent in Hereditary Nonpolyposis Colorectal Cancer Families With Normal pMSH6 Expression as Detected by ImmunohistochemistryThe results of gynecologic surveillance in families with hereditary nonpolyposis colorectal cancerCost-effectiveness of surveillance programs for families at high and moderate risk of hereditary non-polyposis colorectal cancerPresymptomatic diagnosis using a deletion of a single codon in families with hereditary non-polyposis colorectal cancerLack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report
P50
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P50
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P31
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