42 results on '"Lasch, Kathryn"'
Search Results
2. Humanistic burden of disease for patients with advanced melanoma in Canada
3. Cross-cultural validity of the thyroid-specific quality-of-life patient-reported outcome measure, ThyPRO
4. Content validity of the PedsQL™ 3.2 Diabetes Module in newly diagnosed patients with Type 1 diabetes mellitus ages 8–45
5. Development and Validation of a Visual Symptom–Specific Patient-Reported Outcomes Instrument for Adults With Cataract Intraocular Lens Implants
6. PRO development: rigorous qualitative research as the crucial foundation
7. Development of a next day functioning measure to assess the impact of sleep disturbance due to restless legs syndrome: The restless legs syndrome-next day impact questionnaire
8. THE POTENTIAL ROLE OF UNEMPLOYMENT BENEFITS IN SHAPING THE MENTAL HEALTH IMPACT OF UNEMPLOYMENT
9. Patients’ Experiences With Cancer-Related Fatigue: A Review and Synthesis of Qualitative Research
10. A Qualitative Analysis of Patient-Reported Symptoms of Anemia
11. Sociocultural Considerations in Chronic Pain and Its Management
12. Evaluation of a Cancer Pain Education Module
13. The Impact of Unemployment on Health and Well-Being
14. Development and content validity of a patient reported outcomes measure to assess symptoms of major depressive disorder
15. The development of the ICIQ‐UAB: A patient reported outcome measure for underactive bladder
16. Patient-reported outcomes in individuals with hepatitis C virus infection treated with elbasvir/grazoprevir
17. Using focus group methods to develop multicultural cancer pain education materials
18. Culture, pain, and culturally sensitive pain care
19. An Assessment of Clinically Important Differences on the Worst Pain Severity Item of the Modified Brief Pain Inventory in Patients with Diabetic Peripheral Neuropathic Pain
20. Patient-reported treatment-related symptom burden for patients with advanced melanoma in Canada
21. Evaluation and performance of a newly developed patient-reported outcome instrument for diarrhea-predominant irritable bowel syndrome in a clinical study population
22. Qualitative modification and development of patient- and caregiver-reported outcome measures for iron chelation therapy
23. Cultural adaptation: translatability assessment and linguistic validation of the patient-reported outcome instrument for irritable bowel syndrome with diarrhea
24. The relation of family violence, employment status, welfare benefits, and alcohol drinking in the United States
25. Patient and Caregiver Perspectives of Factors Associated with Adherence to and Satisfaction with Iron Chelation Therapy
26. The Political Culture of Social Welfare Policy
27. Cross-cultural validity of the thyroid-specific quality-of-life patient-reported outcome measure, ThyPRO
28. Content validity of the PedsQL™ 3.2 Diabetes Module in newly diagnosed patients with Type 1 diabetes mellitus ages 8–45
29. Using primary patient data to identify the symptoms of brain metastases to develop a patient-reported outcome measure.
30. Major Depressive Disorder Patient Reported Outcome Measure
31. The Irritable Bowel Syndrome-Diarrhea (IBS-D) Daily Symptom Diary and Event Log: A Newly Developed Patient-Reported Outcome (PRO) Measure
32. Restless Legs Syndrome-Next Day Impact Questionnaire
33. Validation of the sleep impact scale in patients with major depressive disorder and insomnia
34. Pain assessment in seriously ill patients
35. The Alzheimer functional status instrument: An instrument to assess rehabilitation strategies for Alzheimer patients
36. Birth-cohort changes in the rates of mania
37. Is hands-on experience more effective than didactic workshops in postgraduate cancer pain education?
38. A Protocol Approach to Assessing Medical Technologies
39. The Political Culture of Medical Technology Assessment (Nih, Boundary Spanner, Organization).
40. Job security.
41. 22 - The Political Culture of Social Welfare Policy
42. Chapter 2 - Sociocultural Considerations in Chronic Pain and Its Management
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