Publikationen
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Patients' and physicians' perspectives of shared decision making for psoriasis systemic treatment: associations with sources of information and health literacy
A Systematic Review and Meta-analysis of Factors Associated with Stigma of Dermatologic Disease Psychodermatology and quality of life
Is Social Stigma Responsible for the Poor Psychological Adjustment of People with Visible Skin Disease? A Meta-Analysis
Cumulative Life Course Impairment: systematisches Review zur Bestimmung von Indikatoren
Xerosis cutis und Stigmatisierung: Patientensicht bei Hauterkrankungen und Erkenntnisse über die Auswirkungen einer Hautpflege
Patients’ and physicians’ perspectives on body surface area affected by psoriasis: Links between disease burden, patient-physician (dis)agreement and patient benefits
Validation of the Spanish Wound-QoL Questionnaire.
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Effects of secukinumab on disease burden, patient needs and benefits, and treatment satisfaction in patients with plaque psoriasis across european regions: Patient’s perspective data from the PROSE study
Secukinumab effects on patient reported outcomes in plaque psoriasis across Europe: Data from the PROSE study
Stigma in visible skin diseases - a literature review and development of a conceptual model
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