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(25 - 48 of 57)

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Characteristics of Lynch syndrome associated ovarian cancer
Excluding Lynch syndrome in a female patient with metachronous DNA mismatch repair deficient colon- and ovarian cancer
Evaluation of current prediction models for Lynch syndrome: updating the PREMM5 model to identify PMS2 mutation carriers
Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis?
Inflammatory potential of the diet and colorectal tumor risk in persons with Lynch syndrome
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome
Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registry
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers
Equivalent Helicobacter pylori infection rates in Lynch syndrome mutation carriers with and without a first-degree relative with gastric cancer
Germ-line variants identified by next generation sequencing in a panel of estrogen and cancer associated genes correlate with poor clinical outcome in Lynch syndrome patients
Dietary B vitamin and methionine intake and MTHFR C677T genotype on risk of colorectal tumors in Lynch syndrome: the GEOLynch cohort study
Limited diagnostic value of microsatellite instability associated pathology features in colorectal cancer
Development of in vitro and in vivo functional assays to enable diagnosis of Variants of Uncertain Significance in the common cancer predisposition Lynch syndrome
Multivariate analysis of MLH1 c.1664T > C (p.Leu555Pro) mismatch repair gene variant demonstrates its pathogenicity
Loss of ARID1A expression and its relationship with PI3K-Akt pathway alterations, TP53 and microsatellite instability in endometrial cancer
Inactivation of DNA Mismatch Repair by Variants of Uncertain Significance in the PMS2 Gene
Colorectal surveillance in Lynch syndrome families
Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists
Do lifestyle factors influence colorectal cancer risk in Lynch syndrome?
Genetic modifiers of cancer risk in Lynch syndrome: a review
Value-based healthcare in Lynch syndrome
Genetic variant in the telomerase gene modifies cancer risk in Lynch syndrome
Functional characterization of MLH1 missense variants identified in lynch syndrome patients
Pathological assessment of mismatch repair gene variants in Lynch syndrome: Past, present, and future

Pages