تأثير الاطفال ذوي الاحتياجات الخاصة على جودة حياة الأسرة

Brown, R., MacAdam–Crisp, J., Wang, M., & Iarocci, G. (2006). Family quality of life when there is a child with a developmental disability. J Policy Practice in Intell Disabilities, 3(4), 238-245. http://dx.doi.org/10.1111/j.1741-1130.2006.00085.x

Clark, M., Brown, R., & Karrapaya, R. (2011). An initial look at the quality of life of Malaysian families that include children with disabilities. Journal Of Intellectual Disability Research, 56(1), 45-60. http://dx.doi.org/10.1111/j.1365-2788.2011.01408.x

Dardas, L., & Ahmad, M. (2014). Quality of life among parents of children with autistic

disorder: A sample from the Arab world. Research in Developmental Disabilities, 35(2), 278-287. http://dx.doi.org/10.1016/j.ridd.2013.10.029

Davis, K., & Gavidia-Payne, S. (2009). The impact of child, family, and professional support characteristics on the quality of life in families of young children with disabilities*. Journal of Intellectual And Developmental Disability, 34(2), 153-162. http://dx.doi.org/10.1080/13668250902874608

Eker, L., & Tüzün, E. (2004). An evaluation of quality of life of mothers of children with

cerebral palsy. Disability and Rehabilitation, 26(23), 1354-1359. http://dx.doi.org/10.1080/09638280400000187

Escobar, R. (2005). Worse quality of life for children with newly diagnosed attention-

Deficit/hyperactivity disorder, compared with asthmatic and healthy children. PEDIATRICS, 116(3), e364-e369. http://dx.doi.org/10.1542/peds.2005-0386

 Jokinen, N., & Brown, R. (2005). Family quality of life from the perspective of older parents. Journal of Intellectual Disability Research, 49(10), 789-793. http://dx.doi.org/10.1111/j.1365-2788.2005.00753.x

Karande, S., Bhosrekar, K., Kulkarni, M., & Thakker, A. (2008). Health-related quality of life

of children with newly diagnosed specific learning disability. Journal of Tropical Pediatrics, 55(3), 160-169. http://dx.doi.org/10.1093/tropej/fmn099

Kemp, G., Smith, M., & Segal, J. (2016). Helping children with learning disabilities: practical

parenting tips for home and school. Helpguide. Retrieved 25 February 2016, from http://www.helpguide.org/articles/learning-disabilities/helping-children-with-learning-disabilities.htm

Khanna, R., Madhavan, S., Smith, M., Patrick, J., Tworek, C., & Becker-Cottrill, B. (2010).

Assessment of health-related quality of life among primary caregivers of children with autism spectrum disorders. J Autism Dev Disord, 41(9), 1214-1227. http://dx.doi.org/10.1007/s10803-010-1140-6

Kuhlthau, K., Orlich, F., Hall, T., Sikora, D., Kovacs, E., Delahaye, J., & Clemons, T. (2009).

Health-related quality of life in children with autism spectrum disorders: results from the Autism Treatment Network. J Autism Dev Disord, 40(6), 721-729. http://dx.doi.org/10.1007/s10803-009-0921-2

Lee, L., Harrington, R., Louie, B., & Newschaffer, C. (2007). Children with autism: quality of

life and parental concerns. J Autism Dev Disord, 38(6), 1147-1160. http://dx.doi.org/10.1007/s10803-007-0491-0

Lukemeyer, A., Meyers, M., & Smeeding, T. (2000). Expensive Children in Poor Families: Out-of-Pocket Expenditures for the Care of Disabled and Chronically Ill Children in Welfare Families. J Marriage and Family, 62(2), 399-415. http://dx.doi.org/10.1111/j.1741-3737.2000.00399.x

Mackie, P., Jessen, E., & Jarvis, S. (1998). The lifestyle assessment questionnaire: an instrument

to measure the impact of disability on the lives of children with cerebral palsy and their families. Child: Care, Health and Development, 24(6), 473-486. http://dx.doi.org/10.1046/j.1365-2214.1998.00083.x

Parish, S., Cloud, J., Huh, J., & Henning, A. (2005). Child care, disability, and family structure:

Use and quality in a population-based sample of low-income preschool children. Children And Youth Services Review, 27(8), 905-919. http://dx.doi.org/10.1016/j.childyouth.2004.12.007

Pit-ten Cate, I., Kennedy, C., & Stevenson, J. (2002). Disability and quality of life in spina bifida

and hydrocephalus. Dev Med Child Neurol, 44(05). http://dx.doi.org/10.1017/s0012162201002146

Schneider, J., Gurucharri, L., Gutierrez, A., & Gaebler-Spira, D. (2001). Health-related quality of

life and functional outcome measures for children with cerebral palsy. Dev Med Child Neurol, 43(09), 601. http://dx.doi.org/10.1017/s0012162201001098

Sullivan, P., Juszczak, E., Bachlet, A., Thomas, A., Lambert, B., & Vernon-Roberts, A. et al.

(2004). Impact of gastrostomy tube feeding on the quality of life of carers of children with cerebral palsy. Dev Med Child Neurol, 46(12). http://dx.doi.org/10.1017/s0012162204001392

Viecili, M., & Weiss, J. (2015). Reliability and validity of the pediatric quality of life

inventory with individuals with intellectual and developmental disabilities. American Journal On Intellectual And Developmental Disabilities, 120(4), 289-301. http://dx.doi.org/10.1352/1944-7558-120.4.289

Werner, S., Edwards, M., Baum, N., Brown, I., Brown, R., & Isaacs, B. (2009). Family quality of life among families with a member who has an intellectual disability: an exploratory examination of key domains and dimensions of the revised FQOL Survey. Journal of Intellectual Disability Research, 53(6), 501-511. http://dx.doi.org/10.1111/j.1365-2788.2009.01164.x

Yuen Shan Leung, C., & Wai Ping Li-Tsang, C. (2003). Quality of life of parents who have

children with disabilities. Hong Kong Journal of Occupational Therapy, 13(1), 19-24. http://dx.doi.org/10.1016/s1569-1861(09)70019-1