Meenakshi Jolly to Surveys and Questionnaires
This is a "connection" page, showing publications Meenakshi Jolly has written about Surveys and Questionnaires.
Connection Strength
2.971
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Health and quality of life outcomes. Health Qual Life Outcomes. 2014 Dec 12; 12:173.
Score: 0.337
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Development and validation of the Lupus Impact Tracker: a patient-completed tool for clinical practice to assess and monitor the impact of systemic lupus erythematosus. Arthritis Care Res (Hoboken). 2014 Oct; 66(10):1542-50.
Score: 0.332
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The French-Canadian validation of a disease-specific, patient-reported outcome measure for lupus. Lupus. 2014 Dec; 23(14):1452-9.
Score: 0.328
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Validation of the Cutaneous Lupus Disease Area and Severity Index (CLASI) using physician- and patient-assessed health outcome measures. J Am Acad Dermatol. 2013 Apr; 68(4):618-623.
Score: 0.290
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A brief assessment tool for body image in systemic lupus erythematosus. Body Image. 2012 Mar; 9(2):279-84.
Score: 0.273
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LupusQoL-US benchmarks for US patients with systemic lupus erythematosus. J Rheumatol. 2010 Sep; 37(9):1828-33.
Score: 0.249
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Does Higher Quality of Care in Systemic Lupus Erythematosus Improve Quality of Life? Arthritis Care Res (Hoboken). 2023 06; 75(6):1198-1205.
Score: 0.148
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The Arabic LupusPRO: A Cross-Cultural Validation of a Disease-Specific Patient-Reported Outcome Tool for Quality of Life in Lupus Patients. Lupus. 2020 Nov; 29(13):1727-1735.
Score: 0.125
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Performance and psychometric properties of lupus impact tracker in assessing patient-reported outcomes in pediatric lupus: Report from a pilot study. Lupus. 2020 Nov; 29(13):1781-1789.
Score: 0.125
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Practice patterns in longitudinal lupus care provision: patient and physician perspectives. Lupus. 2017 Dec; 26(14):1556-1561.
Score: 0.100
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The lupus impact tracker is responsive to changes in clinical activity measured by the systemic lupus erythematosus responder index. Lupus. 2017 Apr; 26(4):396-402.
Score: 0.095
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Validation of the Lupus Impact Tracker in an Australian patient cohort. Lupus. 2017 Jan; 26(1):98-105.
Score: 0.094
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Caregiving, dyadic quality of life and dyadic relationships in lupus. Lupus. 2015 Aug; 24(9):918-26.
Score: 0.085
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Body image intervention to improve health outcomes in lupus: a pilot study. J Clin Rheumatol. 2014 Dec; 20(8):403-10.
Score: 0.084
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Turkish lupusPRO: cross-cultural validation study for lupus. Clin Rheumatol. 2014 Aug; 33(8):1079-84.
Score: 0.077
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Psychometric properties of the EuroQol-5D and Short Form-6D in patients with systemic lupus erythematosus. J Rheumatol. 2009 Jun; 36(6):1209-16.
Score: 0.057
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How does quality of life of patients with systemic lupus erythematosus compare with that of other common chronic illnesses? J Rheumatol. 2005 Sep; 32(9):1706-8.
Score: 0.044
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Korean LupusPRO: Cross-Cultural validation study for systemic lupus erythematosus. Lupus. 2022 Oct; 31(12):1498-1507.
Score: 0.036
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Validation of SIMPLE Index for Lupus Disease Activity. J Clin Rheumatol. 2018 Sep; 24(6):313-318.
Score: 0.027
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The Japanese LupusPRO: A cross-cultural validation of an outcome measure for lupus. Lupus. 2017 Jul; 26(8):849-856.
Score: 0.024
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Indices to assess patients with systemic lupus erythematosus in clinical trials, long-term observational studies, and clinical care. Clin Exp Rheumatol. 2014 Sep-Oct; 32(5 Suppl 85):S-85-95.
Score: 0.021
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Pain and depression predict self-reported fatigue/energy in lupus. Lupus. 2013 Jun; 22(7):684-9.
Score: 0.019