Burden of disease during quiescent periods in patients with pemphigus

The three dimensions of skin disease burden: ‘now’, ‘long term’ and ‘family’

(2013) A.Y. Finlay   BRITISH JOURNAL OF DERMATOLOGY

The development and validation of the Treatment of Autoimmune Bullous Disease Quality of Life questionnaire, a tool to measure the quality of life impacts of treatments used in patients with autoimmune blistering disease

(2013) A. Tjokrowidjaja et al.   BRITISH JOURNAL OF DERMATOLOGY

Development of a Quality-of-Life Instrument for Autoimmune Bullous Disease

(2013) Deshan F. Sebaratnam et al.   JAMA Dermatology

Quality of life in patients with pemphigus receiving adjuvant therapy

(2012) A. Paradisi et al.   CLINICAL AND EXPERIMENTAL DERMATOLOGY

Pemphigus and Quality of Life

(2011) Shien-Ning Chee et al.   DERMATOLOGIC CLINICS

Quality of life and psychological status of patients with pemphigus vulgaris using Dermatology Life Quality Index and General Health Questionnaires

(2011) S. Zahra GHODSI et al.   JOURNAL OF DERMATOLOGY

Psychological distress and investment in one’s appearance in patients with pemphigus

(2010) E Mazzotti et al.   JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY

Reliability and Convergent Validity of Two Outcome Instruments for Pemphigus

(2009) Misha Rosenbach et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

The health impact of pemphigus vulgaris and pemphigus foliaceus assessed using the Medical Outcomes Study 36-item short form health survey questionnaire

(2008) S. Tabolli et al.   BRITISH JOURNAL OF DERMATOLOGY

Consensus statement on definitions of disease, end points, and therapeutic response for pemphigus

(2008) Dedee F. Murrell et al.   JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY

Quality-of-life assessment in patients with pemphigus using a minimum set of evaluation tools

(2008) Andrea Paradisi et al.   JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY