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1. Dominantly inherited micro-satellite instable cancer – the four Lynch syndromes - an EHTG, PLSD position statement

2. 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

5. Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

6. Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

7. Relatives from hereditary breast and ovarian cancer and lynch syndrome families forgoing genetic testing: findings from the Swiss CASCADE cohort

8. Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database (Genetics in Medicine, (2020), 22, 1, (15-25), 10.1038/s41436-019-0596-9)

10. Uptake of hysterectomy and bilateral salpingooophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

11. Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

12. No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study

13. Recommendations to improve identification of hereditary and familial colorectal cancer in Europe

14. Analysis in the Prospective Lynch Syndrome Database identifies sarcoma as part of the Lynch syndrome tumor spectrum

16. Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database (vol 22, pg 15, 2020)

17. Risk-Reducing Gynecological Surgery in Lynch Syndrome: Results of an International Survey from the Prospective Lynch Syndrome Database

18. Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

19. Connective Cards to Interrogate the Museum

20. Disease severity and genetic pathways in attenuated familial adenomatous polyposis vary greatly but depend on the site of the germline mutation

21. An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome

25. LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients

27. Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report

28. An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome.

31. The evolutionary landscape of colorectal tumorigenesis

34. Attenuated familial adenomatous polyposis: results from an international collaborative study

35. Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion

37. Recurrent chromosomal gains and heterogeneous driver mutations characterise papillary renal cancer evolution

42. Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

44. Cancer risk and genotype-phenotype correlations in PTEN hamartoma tumor syndrome

49. Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

50. Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

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