Quality of life in patients with bullous dermatoses

This publication has 27 references indexed in Scilit:

• Quality of life evaluation in epidermolysis bullosa (EB) through the development of the QOLEB questionnaire: an EB-specific quality of life instrument
  British Journal of Dermatology, 2009
• Reliability and Convergent Validity of Two Outcome Instruments for Pemphigus
  Journal of Investigative Dermatology, 2009
• Main Problems Experienced by Children with Epidermolysis Bullosa: a Qualitative Study with Semi-structured Interviews
  Acta Dermato-Venereologica, 2008
• Highlights from the Report of the Working Group on “Core Measures of the Burden of Skin Diseases”
  Journal of Investigative Dermatology, 2007
• Dermatology Quality of Life Instruments: Sorting Out the Quagmire
  Journal of Investigative Dermatology, 2007
• Measuring quality of life of patients with different clinical types of psoriasis using the SF-36
  British Journal of Dermatology, 2006
• Deutliche Einschränkung der Lebensqualität bei Patienten mit Pemphigus vulgaris: Ergebnisse der deutschen Bullous Skin Disease (BSD)‐Studiengruppe
  JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2005
• Impact of inherited epidermolysis bullosa on parental interpersonal relationships, marital status and family size
  British Journal of Dermatology, 2005
• The World Health Organization quality of life assessment (WHOQOL): Position paper from the World Health Organization
  Social Science & Medicine, 1995
• The MOS 36-ltem Short-Form Health Survey (SF-36)
  Medical Care, 1992