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REFERENCES

  • 1
    Porter RJ, Diagnosis of partial seizures. In: PenryJK, ed. Epilepsy: diagnosis, management, quality of life. New York : Raven Press, 1986;135.
  • 2
    Jacoby A., Epilepsy and the quality of every day life: findings from a study of people with well-controlled epilepsy. Soc Sci Med 1992;34:65766.
  • 3
    Scneider J, Conrad P., In the closet with illness: epilepsy, stigma potential and information control. Soc Probl 1980;28:3244.
  • 4
    Scambler G, Hopkins A., Accommodating epilepsy in families. In: AndersonR, BuryM, eds. Living with chronic illness: the experience of patients and their families. London : Allen and Unwin, 1988:15676.
  • 5
    The first 10 years of the World Health Organization. Geneva : World Health Organization, 1958.
  • 6
    Schipper H, Clinch J, Powell V., Definitions and conceptual issues. In: SpikerB, ed. Quality of life assessments in clinical trials. New York : Raven Press, 1990:1124.
  • 7
    Jacoby A, Johnson AL, Chadwick DW, Psychosocial outcomes of antiepileptic drug discontinuation. Epilepsia 1992;33:112331.
  • 8
    Vickrey BG, Hays RD, Graber J, Rausch R, Engel J, Brook RH, A health-related quality of life instrument for patients evaluated for epilepsy surgery. Med Care 1992;30:299319.
  • 9
    Smith DF, Baker GA, Davis G, et al. Outcome of add-on treatment lamotrigine in partial epilepsy. Epilepsia 1993;34:31222.
  • 10
    Baker GA, Jacoby A, Smith DF, Dewed ME, Chadwick DW, Development of a novel scale to assess life fulfillment as part of the further refinement of a quality-of-life model for epilepsy. Epilepsia 1994;35:5916.
  • 11
    Jacoby A, Baker G, Smith D, Dewey M, Chadwick D., Measuring the impact of epilepsy: the development of a novel scale. Epilepsy Res 1993;16:838.
  • 12
    Devinsky O, Vickrey BG, Cramer J, et al. Development of the quality of life in epilepsy inventory. Epilepsia 1995;36:1089104.
  • 13
    Dodrill C, Batzel L, Quiesser H, Tempkin N., An objective method for the assessment of psychological and social problems among epileptics. Epilepsia 1980;21:12335.
  • 14
    Cramer JA, A clinimetric approach to assessing quality of life in epilepsy. Epilepsia 1993;34(suppl):S813.
  • 15
    Guyath GH, Bombardier C, Tugwell P., Measuring disease-specific quality of life in clinical trials. Can Med Assoc J 1986;134:88995.
  • 16
    Perrine KR, A new quality-of-life inventory for epilepsy patients: interim results. Epilepsia 1993;34(suppl):S2833.
  • 17
    Gilliam F, Kuzniecky R, Faught E, Black L, Carpenter G, Schrodt R., Patient-validated content of epilepsy: specific quality-of-life measurement. Epilepsia 1997;38:2336.
  • 18
    Devinsky O., Quality of life with epilepsy. In: WyllieE, ed. The treatment of epilepsy, principles and practice. 2nd ed. Baltimore : Williams & Wilkins, 1997:114550.
  • 19
    O'Donoghue MF, Duncan JS, Sander JWAS, The subjective handicap of epilepsy: a new approach to measuring treatment outcome. Brain 1998;121:31743.
  • 20
    Horner MM, Rawlins P, Giles K., How parents of children with chronic conditions perceive their own needs. Am J Matern Child Nurs 1987;12:403.
  • 21
    Ward F, Bower BD, A study of certain social aspects of epilepsy in childhood. Dev Med Child Neurol 1978;20(suppl):S150.
  • 22
    Austin JK, Oruche UM, Dunn DW, Levstek DA, New-onset childhood seizures: parent's concerns and needs. Clin Nurs Pract Epilepsy 1995;2:810.
  • 23
    Graves C, Hayes VE, Do nurses and parents of children with chronic conditions agree on parental needs J Pediatr Nurs 1996;11:28899.
  • 24
    Austin JK, Dunn DW, Children with newly diagnosed epilepsy: impact on quality of life. In: ChadwickDW, JacobyA, eds. Quality of life and quality of care in epilepsy update 1993. London : Royal Society of Medicine, 1993.
  • 25
    Matthew WS, Barabas G, Ferrari M., Emotional concomitants of childhood epilepsy. Epilepsia 1982;23:67181.
  • 26
    Cull CA, Cognitive function and behavior in children. In: TrimbleMR, ReynoldsEH, eds. Epilepsy behavior and cognitive function. Chichester , England : John Wiley, 1988:97111.
  • 27
    Rutter M, et al. A neuropsychiatry study in childhood. Clin Dev Med 1970;35/36:17585.
  • 28
    Seidenberg M., Academic achievement and school performance of children with epilepsy. In: HermannBP, SeidenbergM, eds. Childhood epilepsies: neuropsychological, psychosocial and intervention aspects. Chichester , England : John Wiley, 1989:10518.
  • 29
    Hoare P, Kersey S., Psychosocial adjustment of children with chronic epilepsy and their families. Dev Med Child Neurol 1991;33:20115.
  • 30
    West P., The social meaning of epilepsy: stigma as a potential explanation for psychopathology in children. In: WhitmanS, HermannBP, eds. Psychopathology in Epilepsy. Oxford , England : Oxford University Press, 1986:24565.
  • 31
    Gill TM, Feinstein AR, A critical appraisal of the quality of quality-of-life measurements. JAMA 1994;272:61926.
  • 32
    Commission on Classification and Terminology of the International League Against Epilepsy. Proposal for revised classification of epilepsies and epileptic syndromes. Epilepsia 1989;30:38999.
  • 33
    Chaplin JE, Yepez R, Shorvon S, Floyd M., A quantitative approach to measuring the social effects of epilepsy. Neuroepidemiology 1990;9:1518.
  • 34
    Derogatis LR, Lipman RS, Rickels K, Uhlenhuth EH, Cori L., The Hopkins symptom checklist (HSCL): a self reported symptom inventory. Behav Sci 1974;19:115.
  • 35
    Hunt SM, McEwen J, McKenna SP, Measuring health status. London : Croom Helm, 1986.
  • 36
    Austin JK, Dunn D, Huster G, Rose D., Development of scales to measure psychosocial care needs of children with seizures and their parents. J Neurosci Nurs 1998;30:15560.
  • 37
    Austin JK, Concerns and fears of children with seizures. Clin Nurs Pract Epilepsy 1993;1:46.
  • 38
    McNelis A, Musick B, Austin JK, Dunn D, Creasy K., Psychosocial care needs of children with new-onset seizures. J Neurosci Nurs 1998;30:1615.
  • 39
    Shore C, Austin JK, Musick B, Dunn D, McBride A, Creasy K., Psychosocial care needs of parents of children with new-onset seizures. J Neurosci Nurs 1998;30:16974.
  • 40
    Austin JK, Smith MS, Risinger MW, McNeilis AM, Childhood epilepsy and asthma: comparison of quality of life. Epilepsia 1994;35:60815.
  • 41
    Austin JK, Huster GA, Dunn DW, Risinger MW, Adolescents with active or inactive epilepsy or asthma: a comparison of quality of life. Epilepsia 1996;37:122838.