Publications
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Assessing the quality of life of people with chronic wounds by using the cross-culturally valid and revised Wound-QoL questionnaire
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Disease severity and patient needs/benefits in genital psoriasis: Patient-reported improvement after 6±1 months of Apremilast treatment
Interpersonal experiences of stigmatization and sexual impairments, quality of life and depression in patients with psoriasis: The mediating role of social avoidance coping
Disease burden and patient needs/benefits in patients with psoriasis with and without anogenital involvement: Preliminary results from the PsoGen study
Psychosocial function of Vitiligo Patients in the face of Stigmatization: A Systematic Review
Secukinumab effects on patient reported outcomes in plaque psoriasis across Europe: Data from the PROSE study
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
The importance of patient-centered healthcare against comorbid depression and anxiety in patients with psoriasis
Patients’ and physicians’ perspectives on body surface area affected by psoriasis: Links between disease burden, patient-physician (dis)agreement and patient benefits
Cumulative Life Course Impairment: systematisches Review zur Bestimmung von Indikatoren
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