Publications
Showing all years
Psychological (co)morbidity in patients with psoriasis: the impact of pruritus and anogenital involvement on symptoms of depression and anxiety and on body dysmorphic concerns – a cross-sectional study
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A Systematic Review and Meta-analysis of Factors Associated with Stigma of Dermatologic Disease Psychodermatology and quality of life
Development of new measures to capture Cumulative Life Course Imairments (CLCI) in patients with chronic skin diseases
Disease burden and patient needs in women of childbearing age with psoriasis: retrospective analysis from the German PsoBest registries Psoriasis
Patients' and physicians' perspectives of shared decision making for psoriasis systemic treatment: associations with sources of information and health literacy
Measuring wellbeing in psoriasis: Psychometric properties of the WHO-5 questionnaire
A comparative analysis of the predictors, extent and impact of self-stigma in people with psoriasis and atopic dermatitis Psychodermatology and quality of life
Development and validation of an outcome instrument measuring dry skin - the Xerosis Area and Severity Index (XASI).
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Parents with Asthmatic Children, Quality of Life
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Destigmatization of people with skin diseases in body care professions – a study protocol
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