| scholarly article | Q13442814 |
| P2093 | author name string | Janet L Poole | |
| Cindy Mendelson | |||
| P2860 | cites work | Specific psychosocial and behavioral outcomes from the systemic lupus erythematosus self-help course | Q70588816 |
| Qualitative analysis: what it is and how to begin | Q71929632 | ||
| Body image dissatisfaction among women with scleroderma: extent and relationship to psychosocial function | Q73233482 | ||
| The use of the Health Assessment Questionnaire (HAQ) to determine physical disability in systemic sclerosis | Q73463792 | ||
| Patient education in arthritis: randomized controlled trial of a mail-delivered program | Q73521074 | ||
| Scleroderma lung: pathogenesis, evaluation, and current therapy | Q73794640 | ||
| Development and evaluation of a patient education program for persons with systemic sclerosis (scleroderma) | Q79319499 | ||
| Factors related to oral hygiene in persons with scleroderma | Q82443192 | ||
| A reexamination of the effectiveness of self-care education for persons with arthritis | Q30460208 | ||
| Focus group interviews as a data collecting strategy | Q30959366 | ||
| Collecting and analysing qualitative data: issues raised by the focus group | Q32028168 | ||
| The concept of theme as used in qualitative nursing research | Q33914966 | ||
| Chronic disease self-management program: 2-year health status and health care utilization outcomes | Q34095629 | ||
| Arthritis self-management studies: a twelve-year review | Q34361230 | ||
| Evidence suggesting that health education for self-management in patients with chronic arthritis has sustained health benefits while reducing health care costs | Q34362182 | ||
| Life with a rare chronic disease: the scleroderma experience | Q35145411 | ||
| Psychologic factors in scleroderma | Q35169080 | ||
| Grasp pattern variations seen in the scleroderma hand | Q39398259 | ||
| Correlates of the disability index of the health assessment questionnaire: a measure of functional impairment in systemic sclerosis | Q41701251 | ||
| Daily activities and hand function in women with scleroderma. | Q51670934 | ||
| Psychological adjustment to systemic sclerosis. | Q52202743 | ||
| Some notions about assumptions underlying health education. | Q52948625 | ||
| Long-term randomized controlled trials of tailored-print and small-group arthritis self-management interventions. | Q53347754 | ||
| Health-related quality of life in systemic sclerosis as measured by the short form 36: Relationship with clinical and biologic markers | Q61458385 | ||
| P433 | issue | 19 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1492-1501 | |
| P577 | publication date | 2007-10-01 | |
| P1433 | published in | Disability and Rehabilitation | Q5281184 |
| P1476 | title | Become your own advocate: advice from women living with scleroderma | |
| P478 | volume | 29 |
| Q48030991 | "It is about taking grips and not let myself be ravaged by my body": a qualitative study of outcomes from in-patient multidisciplinary rehabilitation for patients with chronic rheumatic diseases |
| Q47349444 | "It's Not Me, It's Not Really Me." Insights From Patients on Living With Systemic Sclerosis: An Interview Study |
| Q37385700 | Comparative analysis of educational needs of patients with rheumatic diseases selected based on the Polish version of the Educational Needs Assessment Tool (Pol-ENAT). |
| Q34905661 | Concepts of functioning and health important to people with systemic sclerosis: a qualitative study in four European countries. |
| Q48477287 | Evaluation of a mail-delivered, print-format, self-management program for persons with systemic sclerosis |
| Q93090532 | Factors associated with quality of life in systemic sclerosis: a cross-sectional study |
| Q34674313 | Factors related to self‐efficacy in persons with scleroderma |
| Q90038046 | Functioning in the emotional sphere and ways of coping with chronic connective tissue disease |
| Q39686272 | Living with scleroderma: patients' perspectives, a phenomenological study |
| Q37586400 | New directions for patient-centred care in scleroderma: the Scleroderma Patient-centred Intervention Network (SPIN). |
| Q88612537 | Randomized Controlled Trial to Evaluate an Internet-Based Self-Management Program in Systemic Sclerosis |
| Q39444550 | Skin and mucosa care in systemic sclerosis--patients' and family caregivers' experiences and expectations of a specific education programme: a qualitative study |
| Q48415515 | Taking charge of systemic sclerosis: a pilot study to assess the effectiveness of an internet self-management program |
| Q36492239 | The educational needs of people with systemic sclerosis: a cross-sectional study using the Dutch version of the Educational Needs Assessment Tool (D-ENAT). |
| Q52655851 | The patient experience of Raynaud's phenomenon in systemic sclerosis. |
Search more.