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Your search keyword '"Colorectal Neoplasms, Hereditary Nonpolyposis psychology"' showing total 107 results

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107 results on '"Colorectal Neoplasms, Hereditary Nonpolyposis psychology"'

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1. 'I Live With Lynch. Cancer Worry Ebbs Into the Background, Then Something Brings It to the Fore.' A Qualitative Interview Study Exploring How Lynch Syndrome Carriers Make Sense of Their Cancer Risks and Implications to Support Decision Making.

2. Perception about benefits and risks related to combined hormonal contraceptives use in women with Lynch syndrome.

3. Hereditary Cancer Syndrome Carriers: Feeling Left in the Corner.

4. Patient reported outcomes after risk-reducing surgery in patients at increased risk of ovarian cancer.

5. Mapping psychosocial interventions in familial colorectal cancer: a rapid systematic review.

6. Genetic discrimination by Australian insurance companies: a survey of consumer experiences.

7. For Women, Lynch Syndrome Is About More than Colon Cancer.

8. Men's experiences of recontact about a potential increased risk of prostate cancer due to Lynch Syndrome: "Just another straw on the stack".

9. The impact of health anxiety on perceptions of personal and children's health in parents with Lynch syndrome.

10. Women's preferences for cancer risk management strategies in Lynch syndrome.

11. Clinical verification of genetic results returned to research participants: findings from a Colon Cancer Family Registry.

12. Educational and Psychosocial Support Needs in Lynch Syndrome: Implementation and Assessment of an Educational Workshop and Support Group.

13. A comparison between Lynch syndrome and sporadic colorectal cancer survivors' satisfaction with their healthcare providers.

14. The Impact of Receiving Predictive Genetic Information about Lynch Syndrome on Individual Colonoscopy and Smoking Behaviors.

15. Evolution of cancer risk assessment and counseling related to psychological, financial and legal implications.

16. Physician trust moderates the relationship between intolerance of uncertainty and cancer worry interference among women with Lynch syndrome.

17. Prognostic Factors for Distress After Genetic Testing for Hereditary Cancer.

18. Reproductive Decision-Making in MMR Mutation Carriers After Results Disclosure: Impact of Psychological Status in Childbearing Options.

19. Patients' Attitudes Towards Disclosure of Genetic Test Results to Family Members: The Impact of Patients' Sociodemographic Background and Counseling Experience.

20. Screening adherence and cancer risk perceptions in colorectal cancer survivors with Lynch-like syndrome.

21. Knowledge and Uptake of Genetic Counseling and Colonoscopic Screening Among Individuals at Increased Risk for Lynch Syndrome and their Endoscopists from the Family Health Promotion Project.

22. Universal tumor screening for Lynch syndrome: Assessment of the perspectives of patients with colorectal cancer regarding benefits and barriers.

23. Psychosocial Impact of Lynch Syndrome on Affected Individuals and Families.

24. Long-term psychosocial and behavioral adjustment in individuals receiving genetic test results in Lynch syndrome.

25. Prevalence and correlates of receiving and sharing high-penetrance cancer genetic test results: findings from the Health Information National Trends Survey.

26. Exploring psychological responses to genetic testing for Lynch Syndrome within the family context.

27. Balancing life with an increased risk of cancer: lived experiences in healthy individuals with Lynch syndrome.

28. Comparison of attitudes regarding preimplantation genetic diagnosis among patients with hereditary cancer syndromes.

29. Communication of genetic test results to family and health-care providers following disclosure of research results.

30. Reflex testing for Lynch syndrome: if we build it, will they come? Lessons learned from the uptake of clinical genetics services by individuals with newly diagnosed colorectal cancer (CRC).

31. Psychosocial consequences of predictive genetic testing for Lynch syndrome and associations to surveillance behaviour in a 7-year follow-up study.

32. The role of religious and existential well-being in families with Lynch syndrome: prevention, family communication, and psychosocial adjustment.

33. Communicating cancer risk within an African context: experiences, disclosure patterns and uptake rates following genetic testing for Lynch syndrome.

34. Lynch syndrome: the patients' perspective.

35. 100 years Lynch syndrome: what have we learned about psychosocial issues?

36. On the limits of genetic responsibility: communication and consent for tumour testing for Lynch syndrome.

37. Preferences for outcomes associated with decisions to undergo or forgo genetic testing for Lynch syndrome.

38. Psychological distress in newly diagnosed colorectal cancer patients following microsatellite instability testing for Lynch syndrome on the pathologist's initiative.

39. Colorectal cancer survivors' interest in genetic testing for hereditary cancer: implications for universal tumor screening.

40. The introduction of a choice to learn pre-symptomatic DNA test results for BRCA or Lynch syndrome either face-to-face or by letter.

41. Experiences of living with increased risk of developing colorectal and gynaecological cancer in individuals with no identified gene mutation.

42. Limited impact on self-concept in individuals with Lynch syndrome; results from a national cohort study.

43. Factors affecting encouragement of relatives among families with Lynch syndrome to seek medical assessment.

44. The importance of older family members in providing social resources and promoting cancer screening in families with a hereditary cancer syndrome.

45. Endometrial cancer patients and compliance with genetic counseling: room for improvement.

46. Development and validation of an instrument to measure the impact of genetic testing on self-concept in Lynch syndrome.

47. Attitudes toward childbearing and prenatal testing in individuals undergoing genetic testing for Lynch syndrome.

48. Validation of a self-concept scale for Lynch syndrome in different nationalities.

49. Beliefs about cancer and diet among those considering genetic testing for colon cancer.

50. Colonoscopy use following mutation detection in Lynch syndrome: exploring a role for cancer screening in adaptation.

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