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228 results on '"Amsterdam criteria"'

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1. Placental lesions in birth asphyxia and hypoxic ischemic syndrome.

2. Enhancing the Diagnostic Accuracy of Placental Pathology by Using the Amsterdam Consensus Criteria.

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3. When guidelines face reality — Lynch syndrome screening in the setting of public health system in a developing country

4. Interval between the First Cancer and the Genetic Diagnosis in Lynch Syndrome Probands

5. SINDROMES HEREDITARIOS QUE PREDISPONEN AL DESARROLLO DEL CANCER COLORRECTAL.

6. Quadruple gastrointestinal cancer with discordance of mismatch repair protein deficiency and microsatellite instability suggesting Lynch syndrome

7. Placental histology predicted adverse outcomes in extremely premature neonates in Norway-population-based study

8. Clinical, anamnestic, molecular and genetic criteria for Lynch syndrome

9. Cumulative risks of colorectal cancer in Han Chinese patients with Lynch syndrome in Taiwan

10. A Novel Stop-Gain Mutation in MSH2 Gene Among a Persian Family Fulfilling Classic Amsterdam Criteria for Lynch Syndrome

11. Third‐trimester placentas of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2)‐positive women: histomorphology, including viral immunohistochemistry and in‐situ hybridization

12. New Pathogenic Germline Variants in Very Early Onset and Familial Colorectal Cancer Patients

13. Impact of colonoscopic screening in Familial Colorectal Cancer Type X

14. Polymorphisms of DNA repair genes are associated with colorectal cancer in patients with Lynch syndrome

15. Metachronous colorectal cancer following segmental or extended colectomy in Lynch syndrome: a systematic review and meta-analysis

16. Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy

17. SETD6 dominant negative mutation in familial colorectal cancer type X

18. Hereditary factors are unlikely behind unusual pattern of early - Onset colorectal cancer in Egyptians: A study of family history and pathology features in Egyptians with large bowel cancer (cross-sectional study)

19. Individualized Medicine in Gastroenterology and Hepatology

21. Characterisation of heterozygous PMS2 variants in French patients with Lynch syndrome

22. Effective Identification of Lynch Syndrome in Gastroenterology Practice

23. Carcinoma of the colon in a 40 year old female: a case report

24. MLH1 germline mutation associated with Lynch syndrome in a family followed for more than 45 years

25. DNA copy number profiling in microsatellite-stable and microsatellite-unstable hereditary non-polyposis colorectal cancers by targeted CNV array

26. Lynch syndrome and exposure to aristolochic acid in upper-tract urothelial carcinoma: its clinical impact?

27. Testing strategies to reduce morbidity and mortality from Lynch syndrome

28. Evolving approach and clinical significance of detecting DNA mismatch repair deficiency in colorectal carcinoma

29. Abstract P4-12-08: Utilizing next generation sequencing technologies for hereditary breast cancer risk assessments in a private oncology practice

30. Mismatch repair gone awry: Management of Lynch syndrome

31. Frequency and phenotypic spectrum of germline mutations inPOLEand seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas

32. Cancer Risk in Families Fulfilling the Amsterdam Criteria for Lynch Syndrome

33. Familial Colorectal Cancer Type X

34. Endoscopic Therapy of Biliary Injury After Cholecystectomy

35. A Randomized Trial to Increase Colonoscopy Screening in Members of High-Risk Families in the Colorectal Cancer Family Registry and Cancer Genetics Network

36. Investigation on the hereditary basis of colorectal cancers in an African population with frequent early onset cases

37. A pooled analysis of the outcome of prospective colonoscopic surveillance for familial colorectal cancer

38. Criteria and prediction models for mismatch repair gene mutations: a review

39. High incidence of large deletions in thePMS2gene in Spanish Lynch syndrome families

40. Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucins

41. Historical review of Lynch syndrome

42. Association between the Lynch syndrome gene MSH2 and breast cancer susceptibility in a Canadian familial cancer registry

43. Phenotypic Heterogeneity by Germline Mismatch Repair Gene Defect in Lynch Syndrome Patients

44. Two novel sequence variants in MSH2 gene in a patient who underwent cancer genetic counseling for a very early-onset epithelial ovarian cancer

45. Genetic screening in young women diagnosed with endometrial cancer

46. MLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome

47. Use of SSCP analysis to identify germline mutations in HNPCC families fulfilling the Amsterdam criteria

48. Observational Study: Familial Relevance and Oncological Significance of Revised Bethesda Guidelines in Colorectal Patients That Have Undergone Curative Resection

49. A case of multiple primary malignancies and investigation of family history

50. The comparasion of microsatellite instability at sporadic colorectal and hereditary non-polyposis colorectal cancers