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Factors affecting quality of life in epidermolysis bullosa

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Pages 329-338 | Published online: 09 Jan 2014

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Nicholas H. B. Schräder, Eva W. H. Korte, José C. Duipmans, Roy E. Stewart, Maria C. Bolling & André P. Wolff. (2021) Identifying Epidermolysis Bullosa Patient Needs and Perceived Treatment Benefits: An Explorative Study Using the Patient Benefit Index. Journal of Clinical Medicine 10:24, pages 5836.
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Sandra Kearney, Ann Donohoe & Eilish McAuliffe. (2020) Living with epidermolysis bullosa: Daily challenges and health‐care needs. Health Expectations 23:2, pages 368-376.
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Rebecca Cross Bodán. (2020) Reframing the Care of Children With Epidermolysis Bullosa Through the Lens of Medical Trauma. Journal of the Dermatology Nurses' Association 12:1, pages 16-23.
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Kristin Iversen, Lill Monica Drivdal, Kristin J. Billaud Feragen & Amy Østertun Geirdal. (2018) Quality of life in adults with lymphedema cholestasis syndrome 1. Health and Quality of Life Outcomes 16:1.
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In Kyung JeonHye Rang OnSoo-Chan Kim. (2016) Quality of Life and Economic Burden in Recessive Dystrophic Epidermolysis Bullosa. Annals of Dermatology 28:1, pages 6.
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F. Sampogna, S. Tabolli, C. Di Pietro, D. Castiglia, G. Zambruno & D. Abeni. (2013) The evaluation of family impact of recessive dystrophic epidermolysis bullosa using the Italian version of the Family Dermatology Life Quality Index. Journal of the European Academy of Dermatology and Venereology 27:9, pages 1151-1155.
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