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A Systematic Review and Meta-analysis of Factors Associated with Stigma of Dermatologic Disease Psychodermatology and quality of life
Dermatological care of elderly people with psoriasis before and after entering a nursing home: A qualitative analysis from the perspective of medical providers
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Is Social Stigma Responsible for the Poor Psychological Adjustment of People with Visible Skin Disease? A Meta-Analysis
Patients' and physicians' perspectives of shared decision making for psoriasis systemic treatment: associations with sources of information and health literacy
Stigma in visible skin diseases - a literature review and development of a conceptual model
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Patient-reported outcomes measures – measuring wellbeing not only burden of disease
Effectiveness of a structured short intervention against stigmatisation in chronic visible skin diseases: Results of a controlled trial in future educators
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Secukinumab effects on disease burden, patient needs and benefits, and treatment satisfaction in patients with plaque psoriasis across European regions: patient perspective data from the PROSE study
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Assessment of stigma related to visible skin diseases: a systematic review and evaluation of patient-reported outcome measures
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Exploring the burden of xerosis cutis and the impact of dermatological skin care from patient's perspective
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