Citations (22)
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Hiroki Tanabe, Toshihiko Shiraishi, Haruhiko Sato, Misato Nihei, Takenobu Inoue & Chika Kuwabara. (2023) A concept for emotion recognition systems for children with profound intellectual and multiple disabilities based on artificial intelligence using physiological and motion signals. Disability and Rehabilitation: Assistive Technology 0:0, pages 1-8.
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Christina N. Marsack-Topolewski. (2022) Predictors of quality of life for aging family caregivers of adults with autism. Journal of Family Social Work 25:2-3, pages 109-125.
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Yueh-Ching Chou, Shih-Chih Wang, Heng-Hao Chang & Li-Yeh Fu. (2014) Working but not employed: Mothers of adults with intellectual disability as hidden workers. Journal of Intellectual & Developmental Disability 39:4, pages 353-362.
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Articles from other publishers (19)
Bephyer Parey. (2022) Measurement, Associated Factors, and Gender Implications of Care Views towards Older Persons with Disabilities: The Case of Trinidad. Ageing International 48:2, pages 501-525.
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Salih Rakap, Meryem Vural-Batik, Sinan Kalkan, Mustafa Karnas, Halil Ibrahim Sari & Uygar Bayrakdar. (2022) The hidden (overlooked) impact of living through a pandemic: How parents of children with disabilities fared during COVID-19?. Frontiers in Education 7.
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Rakgadi Grace Malapela & Gloria Thupayagale-Tshweneagae. (2022) Enablers to enhance school-based adolescents with intellectual disabilities’ learning: A narrative approach. Journal of Intellectual Disabilities, pages 174462952211419.
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Stacy Davenport & Tara Rava Zolnikov. (2021) Understanding mental health outcomes related to compassion fatigue in parents of children diagnosed with intellectual disability. Journal of Intellectual Disabilities 26:3, pages 624-636.
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Kai Yip Choi, Ho Yin Wong, Hoi Nga Cheung, Jung Kai Tseng, Ching Chung Chen, Chieh Lin Wu, Helen Eng, George C. Woo & Allen Ming Yan Cheong. (2022) Impact of visual impairment on balance and visual processing functions in students with special educational needs. PLOS ONE 17:4, pages e0249052.
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Chun-Yu Chiu. (2021) Bamboo Sibs: Experiences of Taiwanese Non-disabled Siblings of Adults with Intellectual and Developmental Disabilities across Caregiver Lifestages. Journal of Developmental and Physical Disabilities 34:2, pages 233-253.
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Varsha Patel, Gisela Perez‐Olivas, Biza Stenfert Kroese, Gemma Rogers, John Rose, Glynis Murphy, Vivien Cooper, Peter E Langdon, Steve Hiles, Clair Clifford & Paul Willner. (2021)
The Experiences of Carers of Adults With Intellectual Disabilities During the First
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Cristina Jenaro, Noelia Flores, Belén Gutiérrez-Bermejo, Vanessa Vega, Carmen Pérez & Maribel Cruz. (2020) Parental Stress and Family Quality of Life: Surveying Family Members of Persons with Intellectual Disabilities. International Journal of Environmental Research and Public Health 17:23, pages 9007.
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Marie-Christine Rousseau, Karine Baumstarck, Maria Valkov, Agnés Felce, Catherine Brisse, Sherezad Khaldi-Cherif, Anderson Loundou, Pascal Auquier & Thierry Billette de Villemeur. (2020) Impact of severe polyhandicap cared for at home on French informal caregivers’ burden: a cross-sectional study. BMJ Open 10:1, pages e032257.
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Stephania A. Rodrigues, Bruno J. B. Fontanella, Lucimar R. S. de Avó, Carla M. R. Germano & Débora G. Melo. (2019) A qualitative study about quality of life in Brazilian families with children who have severe or profound intellectual disability. Journal of Applied Research in Intellectual Disabilities 32:2, pages 413-426.
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Pasang Doma Sherpa, Luppana Kitrungrote & Wipa Sae-Sia. (2018) Predicting quality of life among family caregivers of people with spinal cord injury having chronic low back pain in Nepal: a cross-sectional pilot study. Spinal Cord Series and Cases 4:1.
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Shixi Zhao, Chen-Hui Wang, Tse-Yang Huang, Yann-Jang Chen, Ching-Hua Hsiao, Chie-Chien Tseng, Lei Xu & Lei-Shih Chen. (2018) A qualitative study exploring the attitudes toward prenatal genetic testing for autism spectrum disorders among parents of affected children in Taiwan. Research in Autism Spectrum Disorders 48, pages 36-43.
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Jillian M. Grey, Vasiliki Totsika & Richard P. Hastings. (2018) Physical and psychological health of family carers co-residing with an adult relative with an intellectual disability. Journal of Applied Research in Intellectual Disabilities 31, pages 191-202.
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A. Kamstra, A. A. J. van der Putten & C. Vlaskamp. (2015) The Structure of Informal Social Networks of Persons with Profound Intellectual and Multiple Disabilities. Journal of Applied Research in Intellectual Disabilities 28:3, pages 249-256.
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Hiroshi Ihara, Hiroyuki Ogata, Masayuki Sayama, Aya Kato, Masao Gito, Nobuyuki Murakami, Yasuhiro Kido & Toshiro Nagai. (2014) QOL in caregivers of Japanese patients with Prader–Willi syndrome with reference to age and genotype. American Journal of Medical Genetics Part A 164:9, pages 2226-2231.
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C-Y. Hsiao. (2014) Family demands, social support and family functioning in Taiwanese families rearing children with Down syndrome. Journal of Intellectual Disability Research 58:6, pages 549-559.
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Carmel McDougall, Angus Buchanan & Sunila Peterson. (2014) Understanding primary carers' occupational adaptation and engagement. Australian Occupational Therapy Journal 61:2, pages 83-91.
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Tina O’Connell, Maeve O’Halloran & Owen Doody. (2013) Raising a child with disability and dealing with life events. Journal of Intellectual Disabilities 17:4, pages 376-386.
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Yueh-Ching Chou, Yue-Chune Lee, Shu-chuan Chang & Amy Pei-Lung Yu. (2013) Evaluating the supports intensity scale as a potential assessment instrument for resource allocation for persons with intellectual disability. Research in Developmental Disabilities 34:6, pages 2056-2063.
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