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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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DOI:
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
Assessment of stigma related to visible skin diseases: a systematic review and evaluation of patient-reported outcome measures
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Disease severity and patient needs/benefits in genital psoriasis: Patient-reported improvement after 6±1 months of Apremilast treatment
Exploring the burden of xerosis cutis and the impact of dermatological skin care from patient's perspective
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DOI:
Secukinumab effects on patient reported outcomes in plaque psoriasis across Europe: Data from the PROSE study
Patients’ and physicians’ perspectives on body surface area affected by psoriasis: Links between disease burden, patient-physician (dis)agreement and patient benefits
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