77 results on '"Møller, Pal"'
Search Results
2. Dominantly inherited micro-satellite instable cancer – the four Lynch syndromes - an EHTG, PLSD position statement
3. Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database
4. Delphi Initiative for Early-Onset Colorectal Cancer (DIRECt) International Management Guidelines
5. Contraceptive use and the risk of ovarian cancer among women with a BRCA1 or BRCA2 mutation
6. Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants
7. The Manchester International Consensus Group recommendations for the management of gynecological cancers in Lynch syndrome
8. Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
9. Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
10. Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
11. Long-term outcomes following a diagnosis of ovarian cancer at the time of preventive oophorectomy among BRCA1 and BRCA2 mutation carriers
12. Delineating genotype and parent‐of‐origin effect on the phenotype in MSH6‐associated Lynch syndrome
13. Risk Factors For Endometrial Cancer Among Women With A BRCA1 Or BRCA2 Mutation
14. Treatment Of Infertility And Risk Of Breast Cancer Among Women With A BRCA Mutation: A Matched Case-Control Study
15. Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
16. Delineating genotype and parent-of-origin effect on the phenotype in MSH6-associated Lynch syndrome
17. Delineating genotype and parent-of-origin effect on the phenotype in MSH6-associated Lynch syndrome
18. A snapshot of current genetic testing practice in Lynch syndrome: The results of a representative survey of 33 Latin American existing centres/registries
19. Ancient genomes from Iceland reveal the making of a human population
20. The Prospective Lynch Syndrome Database
21. Databases: Intentions, Capabilities, and Limitations
22. Age-specific ovarian cancer risks among women with a BRCA1 or BRCA2 mutation
23. The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers
24. Treatment of infertility does not increase the risk of ovarian cancer among women with a BRCA1 or BRCA2 mutation
25. Risk reducing mastectomy, breast reconstruction and patient satisfaction in Norwegian BRCA1/2 mutation carriers
26. The incidence of endometrial cancer in women with BRCA1 and BRCA2 mutations: An international prospective cohort study
27. Infertility, Treatment of Infertility, and the Risk of Breast Cancer among Women with BRCA1 and BRCA2 Mutations: A Case-Control Study
28. Quality of Life and Its Relation to Cancer-Related Stress in Women of Families with Hereditary Cancer without Demonstrated Mutation
29. Alcohol consumption and the risk of breast cancer among BRCA1 and BRCA2 mutation carriers
30. Cancer risk and genotype–phenotype correlations in PTEN hamartoma tumor syndrome
31. Inherited Breast Cancer
32. Prophylactic bilateral salpingo-oophorectomy (PBSO) with or without prophylactic bilateral mastectomy (PBM) or no intervention in BRCA1 mutation carriers: A cost-effectiveness analysis
33. Reproductive risk factors for ovarian cancer in carriers of BRCA1 or BRCA2 mutations: a case-control study
34. Sensitivity of MRI versus conventional screening in the diagnosis of BRCA-associated breast cancer in a national prospective series
35. Genetic epidemiology of BRCA mutations – family history detects less than 50% of the mutation carriers
36. The risk of endometrial cancer in women with BRCA1 and BRCA2 mutations. A prospective study
37. Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
38. Screening mammography and risk of breast cancer in BRCA1 and BRCA2 mutation carriers: a case-control study
39. Hormone replacement therapy and the risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers
40. A Combined Genomewide Linkage Scan of 1,233 Families for Prostate Cancer–Susceptibility Genes Conducted by the International Consortium for Prostate Cancer Genetics
41. Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance
42. Comprehensive characterisation of Lynch syndrome and screening strategies: a cohort study of individuals at risk from Latin American genetic registries
43. Suggestive evidence for a site specific prostate cancer gene on chromosome 1p36
44. Response to Chambuso et al
45. Towards evidence-based personalised precision medicine for Lynch syndrome
46. eP551 - Weight gain and the risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers
47. Cancer Risks for PMS2-associated lynch syndrom
48. Cancer Risks for PMS2-associated lynch syndrom
49. Penetrances of BRCA1 1675delA and 1135insA with Respect to Breast Cancer and Ovarian Cancer
50. Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
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