1. Lefley HP. Family burden and family stigma in major mental illness. Am Psychol. 1989. 44:556–560.
Article
2. Gibbons JS, Horn SH, Powell JM, Gibbons JL. Schizophrenic patients and their families. A survey in a psychiatric service based on a DGH unit. Br J Psychiatry. 1984. 144:70–77.
Article
3. Hatfield AB. Help-seeking behavior in families of schizophrenics. Am J Community Psychol. 1979. 7:563–569.
Article
4. Rössler W, Salize HJ, Cucchiaro G, Reinhard I, Kernig C. Does the place of treatment influence the quality of life of schizophrenics? Acta Psychiatr Scand. 1999. 100:142–148.
Article
5. Björkman T, Hansson L. Predictors of improvement in quality of life of long-term mentally ill individuals receiving case management. Eur Psychiatry. 2002. 17:33–40.
Article
6. Kaltiala-Heino R, Laippala P, Joukamaa M. Has the attempt to reduce psychiatric inpatient treatment been successful in Finland? Eur Psychiatry. 2001. 16:215–221.
Article
7. Fadden G, Bebbington P, Kuipers L. The burden of care: the impact of functional psychiatric illness on the patient's family. Br J Psychiatry. 1987. 150:285–292.
Article
8. Ostman M, Hansson L, Andersson K. Family burden, participation in care and mental health--an 11-year comparison of the situation of relatives to compulsorily and voluntarily admitted patients. Int J Soc Psychiatry. 2000. 46:191–200.
Article
9. Goldman HH. Mental illness and family burden: a public health perspective. Hosp Community Psychiatry. 1982. 33:557–560.
Article
10. Hoenig J, Hamilton MW. The schizophrenic patient in the community and his effect on the household. Int J Soc Psychiatry. 1966. 12:165–176.
Article
11. Vaughn CE, Leff JP. The influence of family and social factors on the course of psychiatric illness. A comparison of schizophrenic and depressed neurotic patients. Br J Psychiatry. 1976. 129:125–137.
Article
12. Barrowclough C, Tarrier N. 'Psychosocial' interventions with families and their effects on the course of schizophrenia: a review. Psychol Med. 1984. 14:629–642.
Article
13. Mandelbrote B, Folkard S. Some problems and needs of schizophrenics in relation to a developing psychiatric community service. Compr Psychiatry. 1961. 2:317–328.
Article
14. Schene AH. Objective and subjective dimensions of family burden. Towards an integrative framework for research. Soc Psychiatry Psychiatr Epidemiol. 1990. 25:289–297.
Article
15. Grad J, Sainsbury P. Mental illness and the family. Lancet. 1963. 1:544–547.
Article
16. Hoenig J. The de-segregation of the psychiatric patient. Proc R Soc Med. 1968. 61:115–120.
17. Pai S, Kapur RL. The burden on the family of a psychiatric patient: development of an interview schedule. Br J Psychiatry. 1981. 138:332–335.
Article
18. Platt S, Weyman A, Hirsch S, Hewett S. The Social Behaviour Assessment Schedule (SBAS): rationale, contents, scoring and reliability of a new interview schedule. Soc Psychiatry. 1980. 15:43–55.
Article
19. Tessler R, Gamache G. Toolkit for evaluating family experiences with severe mental illness. 1995. Cambridge, MA: Human Services Research Institute.
20. Reinhard SC, Gubman GD, Horwitz AV, Minsky S. Burden assessment scale for families of the seriously mentally ill. Eval Program Plann. 1994. 17:261–269.
Article
21. Kim CK, Cho JS, Seo JM, Kim YK, Kim HC, Kim HS, et al. A preliminary study for the development of the family burden scale of the schizophrenics. J Korean Neuropsychiatr Assoc. 1999. 38:539–553.
22. Kim SYJ, Kim SA, Hhun MS, Nam KA. The burden of mental illness on the family and professional support. Yeonsegyoyukgwahak. 1996. 44:93–115.
23. Hogan TP, Awad AG. Subjective response to neuroleptics and outcome in schizophrenia: a re-examination comparing two measures. Psychol Med. 1992. 22:347–352.
Article
24. Awad AG. Subjective response to neuroleptics in schizophrenia. Schizophr Bull. 1993. 19:609–618.
Article
25. Hogan TP, Awad AG, Eastwood R. A self-report scale predictive of drug compliance in schizophrenics: reliability and discriminative validity. Psychol Med. 1983. 13:177–183.
Article
26. Awad AG, Voruganti LN. Neuroleptic dysphoria: revisiting the concept 50 years later. Acta Psychiatr Scand Suppl. 2005. 6–13.
Article
27. Yoon BH, Sea YM, Bae SO, Lee ES, Lee HY. Subjective Response to Atypical and Typical Antipsychotics in Schizophrenic Inpatients. J Korean Soc Biol Ther Psychiatry. 2002. 8:298–304.
Article
28. Kim JH, Yoon JH, Lee JY, No KH, Hong SK, Yoon SC, et al. Subjective quality of life in schizophrenic patients receiving atypical antipsychotics: relationship to psychopathology, adverse drug effects and subjective response to drug. J Korean Neuropsychiatr Assoc. 2003. 42:222–230.
29. Ryu SH. Subjective quality of life in patients with schizophrenia receiving antipsychotics: relationship among subjective quality of life, drug attitude, and side-effect profiles of drugs. Korean J Psychopharmacol. 2005. 16:42–51.
30. Amador XF, Strauss DH, Yale SA, Flaum MM, Endicott J, Gorman JM. Assessment of insight in psychosis. Am J Psychiatry. 1993. 150:873–879.
Article
31. Song JY, Kim KT, Lee SK, Kim YH, Noh JH, Kim JW, et al. Reliability and validity of the Korean version of the Scale to assessment Unawareness of Mental Disorder (SUMD-K). J Korean Neuropsychiatr Assoc. 2006. 45:307–315.
32. Chun BR. Research Methodology. 1994. Department of Preventive Medicine, School of Medicine, Kyungpook National University.
33. Ivarsson AB, Sidenvall B, Carlsson M. The factor structure of the Burden Assessment Scale and the perceived burden of caregivers for individuals with severe mental disorders. Scand J Caring Sci. 2004. 18:396–401.
Article
34. Gopinath PS, Chaturvedi SK. Distressing behaviour of schizophrenics at home. Acta Psychiatr Scand. 1992. 86:185–188.
Article
35. Pearlin LI, Mullan JT, Semple SJ, Skaff MM. Caregiving and the stress process: an overview of concepts and their measures. Gerontologist. 1990. 30:583–594.
Article
36. Pearlin LI, Aneshensel CS, LeBlanc AJ. The forms and mechanisms of stress proliferation: the case of AIDS caregivers. J Health Soc Behav. 1997. 38:223–236.
Article
37. Guada J, Land H, Han J. An exploratory factor analysis of the Burden Assessment Scale with a sample of African-American families. Community Ment Health J. 2011. 47:233–242.
Article
38. Awad AG, Voruganti LN. The burden of schizophrenia on caregivers: a review. Pharmacoeconomics. 2008. 26:149–162.
39. Baronet AM. Factors associated with caregiver burden in mental illness: a critical review of the research literature. Clin Psychol Rev. 1999. 19:819–841.
Article
40. Rosenfarb IS, Bellack AS, Aziz N. A sociocultural stress, appraisal, and coping model of subjective burden and family attitudes toward patients with schizophrenia. J Abnorm Psychol. 2006. 115:157–165.
Article
41. Guarnaccia PJ, Parra P. Ethnicity, social status, and families' experiences of caring for a mentally ill family member. Community Ment Health J. 1996. 32:243–260.
Article