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Original Article

Quality of Life of Swedish Women with Fibromyalgia Syndrome, Rheumatoid Arthritis or Systemic Lupus Erythematosus

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Pages 199-207 | Published online: 16 Jan 2010

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Read on this site (6)

Päivi Juuso, Lisa Skär, Malin Olsson & Siv Söderberg. (2013) Meanings of Feeling Well for Women With Fibromyalgia. Health Care for Women International 34:8, pages 694-706.
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Carol S. Burckhardt, Sharon R. Clark & Robert M. Bennett. (2005) Long-Term Follow-Up of Fibromyalgia Patients Who Completed a Structured Treatment Program versus Patients in Routine Treatment. Journal of Musculoskeletal Pain 13:1, pages 5-14.
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Siv Söderberg & Berit Lundman. (2001) TRANSITIONS EXPERIENCED BY WOMEN WITH FIBROMYALGIA. Health Care for Women International 22:7, pages 617-631.
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B. Strömbeck, C. Ekdahl, R. Manthorpe, I. Wikström, L. Jacobsson. (2000) Health-related quality of life in primary Sjögren's syndrome, rheumatoid arthritis and fibromyalgia compared to normal population data using SF-36. Scandinavian Journal of Rheumatology 29:1, pages 20-28.
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K. Mannerkorpi & C. Ekdahl. (1997) Assessment of Functional Limitation and Disability in Patients with Fibromyalgia. Scandinavian Journal of Rheumatology 26:1, pages 4-13.
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Articles from other publishers (22)

Bradley M Okdie & James H Wirth. (2018) Can Burdensome Facebook “Friends” Cause You Pain? Self-Reported Pain as a Motivation for Exclusion. Journal of Computer-Mediated Communication 23:6, pages 313-331.
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Martin Offenbächer, Sebastian Sauer, Niko Kohls, Millard Waltz & Peter Schoeps. (2011) Quality of life in patients with fibromyalgia: validation and psychometric properties of the German Quality of Life Scale (QOLS-G). Rheumatology International 32:10, pages 3243-3252.
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I Moldovan, E Katsaros, FN Carr, D Cooray, K Torralba, S Shinada, ML Ishimori, M Jolly, DJ Wallace, MH Weisman & PM Nicassio. (2011) The Patient Reported Outcomes in Lupus (PATROL) study: role of depression in health-related quality of life in a Southern California lupus cohort. Lupus 20:12, pages 1285-1292.
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R Ni Riordain, E Moloney, K O’Sullivan & C McCreary. (2010) Burning mouth syndrome and oral health-related quality of life: is there a change over time?. Oral Diseases 16:7, pages 643-647.
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Julian Thumboo & Vibeke Strand. (2007) Health-related Quality of Life in Patients with Systemic Lupus Erythematosus: An Update. Annals of the Academy of Medicine, Singapore 36:2, pages 115-122.
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Målfrid RåheimWenche Håland. (2016) Lived Experience of Chronic Pain and Fibromyalgia: Women's Stories From Daily Life. Qualitative Health Research 16:6, pages 741-761.
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Asani H. Seawell & Sharon Danoff-Burg. (2005) Body Image and Sexuality in Women With and Without Systemic Lupus Erythematosus. Sex Roles 53:11-12, pages 865-876.
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A H SeawellS Danoff-Burg. (2016) Psychosocial research on systemic lupus erythematosus: a literature review. Lupus 13:12, pages 891-899.
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Maria Koutantji, Emma Harrold, Suzanne E. Lane, Shirley Pearce, Richard A. Watts & David G. I. Scott. (2003) Investigation of quality of life, mood, pain, disability, and disease status in primary systemic vasculitis. Arthritis Care & Research 49:6, pages 826-837.
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Lily Neumann, Vladimir Zeldets, Arkady Bolotin & Dan Buskila. (2003) Outcome of posttraumatic fibromyalgia: A 3-year follow-up of 78 cases of cervical spine injuries. Seminars in Arthritis and Rheumatism 32:5, pages 320-325.
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Kristi D. Wright, Gordon J.G. Asmundson & Donald R. McCreary. (2012) Factorial validity of the short‐form McGill pain questionnaire (SF‐MPQ). European Journal of Pain 5:3, pages 279-284.
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Kay Brune, Antje Beyer & Michael SchäferM. Offenbächer. 2001. Schmerz. Schmerz 157 161 .
M. Koutantji, S. Pearce & E. Harrold. (2000) Psychological aspects of vasculitis. Rheumatology 39:11, pages 1173-1179.
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Dan Buskila, Lily Neumann, Ali Alhoashle & Mahmoud Abu-Shakra. (2000) Fibromyalgia syndrome in men. Seminars in Arthritis and Rheumatism 30:1, pages 47-51.
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Lily Neumann, Alexander Berzak & Dan Buskila. (2000) Measuring health status in Israeli patients with fibromyalgiasyndrome and widespread pain and healthy individuals: Utility of the Short Form 36-item health survey (SF-36). Seminars in Arthritis and Rheumatism 29:6, pages 400-408.
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A D Sperber, Y Atzmon, L Neumann, I Weisberg, Y Shalit, M Abu-Shakrah, A Fich & D Buskila. (1999) Fibromyalgia in The Irritable Bowel Syndrome: Studies of Prevalence and Clinical Implications. American Journal of Gastroenterology 94:12, pages 3541-3546.
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Siv SöderbergBerit LundmanAstrid Norberg. (2016) Struggling for Dignity: The Meaning of Women’s Experiences of Living with Fibromyalgia. Qualitative Health Research 9:5, pages 575-587.
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Kaisa Mannerkorpi, Tomas Kroksmark & Charlotte Ekdahl. (2006) How patients with fibromyalgia experience their symptoms in everyday life. Physiotherapy Research International 4:2, pages 110-122.
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Lily Neumann & Dan Buskila. (1997) Quality of life and physical functioning of relativesof fibromyalgia patients. Seminars in Arthritis and Rheumatism 26:6, pages 834-839.
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Dan Buskila, Lily Neumann, Genady Vaisberg, Daphna Alkalay & Frederick Wolfe. (2005) Increased rates of fibromyalgia following cervical spine injury. A Controlled study of 161 cases of traumatic injury. Arthritis & Rheumatism 40:3, pages 446-452.
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Dan Buskila, Lily Neumann, Ilia Hazanov & Rivka Carmi. (1996) Familial aggregation in the fihromyalgia syndrome. Seminars in Arthritis and Rheumatism 26:3, pages 605-611.
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Geoffrey O. Littlejohn. (1995) A DATABASE FOR FIBROMYALGIA. Rheumatic Disease Clinics of North America 21:2, pages 527-557.
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