What do multiple sclerosis patients and their caregivers perceive as unmet needs?
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G. Fenu | J. Frau | M. Marrosu | E. Cocco | G. Mura | L. Lorefice | C. Sardu | M. Melis | G. Coghe | Giulia Coni | Gioia Mura
[1] J. Kira,et al. Structural equation modeling of factors contributing to quality of life in Japanese patients with multiple sclerosis , 2013, BMC Neurology.
[2] J. Benito-León,et al. The CAREQOL-MS was a useful instrument to measure caregiver quality of life in multiple sclerosis. , 2011, Journal of clinical epidemiology.
[3] J. Dunn. Impact of mobility impairment on the burden of caregiving in individuals with multiple sclerosis , 2010, Expert review of pharmacoeconomics & outcomes research.
[4] Celia S. Chen,et al. Multiple sclerosis: patients’ information sources and needs on disease symptoms and management , 2010, Patient preference and adherence.
[5] V. Drennan,et al. Priorities in identifying unmet need in older people attending general practice: a nominal group technique study. , 2007, Family practice.
[6] J. Ohaeri,et al. Relationship of depression, disability, and family caregiver attitudes to the quality of life of Kuwaiti persons with multiple sclerosis: a controlled study , 2007, BMC neurology.
[7] A. While,et al. What people with multiple sclerosis perceive to be important to meeting their needs. , 2007, Journal of advanced nursing.
[8] C. Pozzilli,et al. Effects of education level and employment status on HRQoL in early relapsing-remitting multiple sclerosis , 2007, Multiple sclerosis.
[9] M. Vandervoort,et al. Top 10 needs of people with multiple sclerosis and their significant others. , 2006, The Journal of neuroscience nursing : journal of the American Association of Neuroscience Nurses.
[10] Julián Benito-León,et al. Quality of life and its assessment in multiple sclerosis: integrating physical and psychological components of wellbeing , 2005, The Lancet Neurology.
[11] V. Lehtinen,et al. Psychosocial wellbeing and psychiatric care in the European Communities: analysis of macro indicators , 2004, Social Psychiatry and Psychiatric Epidemiology.
[12] V. Tomassini,et al. Relationship between emotional distress in caregivers and health status in persons with multiple sclerosis , 2004, Multiple sclerosis.
[13] Anthony Feinstein,et al. The Neuropsychiatry of Multiple Sclerosis , 2004, Canadian journal of psychiatry. Revue canadienne de psychiatrie.
[14] H. Boeije,et al. Encountering the downward phase: biographical work in people with multiple sclerosis living at home. , 2002, Social science & medicine.
[15] T. Peters,et al. What do people with MS want and expect from health‐care services? , 2001, Health expectations : an international journal of public participation in health care and health policy.
[16] A J Thompson,et al. A questionnaire assessment of unmet needs for rehabilitation services and resources for people with multiple sclerosis: results of a pilot survey in five European countries , 2000, Clinical rehabilitation.
[17] Nigel V. Marsh,et al. Neuropsychological Aspects of Multiple Sclerosis , 1998, Neuropsychology Review.
[18] A. Sadovnick,et al. Epidemiology of Multiple Sclerosis: A Critical Overview , 1993, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.
[19] Erik K. St. Louis. Scientific Foundations of Obstetrics and Gynecology , 1992, Annals of Internal Medicine.
[20] Stephen M. Rao,et al. Cognitive dysfunction in multiple sclerosis. , 1991, Neurology.
[21] C. Helman. Disease versus illness in general practice. , 1981, The Journal of the Royal College of General Practitioners.
[22] Y. Ono. [Developing effectively therapeutic relationships]. , 2012, Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica.
[23] Hans-Ulrich Prokosch,et al. Use and perception of Internet for health related purposes in Germany: results of a national survey , 2007, International Journal of Public Health.