Advanced search
Publication Cover
Journal of Intellectual & Developmental Disability Volume 34, 2009 - Issue 2
Submit an article Journal homepage
3,793
Views
191
CrossRef citations to date
0
Altmetric
Articles

The impact of child, family, and professional support characteristics on the quality of life in families of young children with disabilitiesFootnote

Kate Davis RMIT University, Melbourne, AustraliaCorrespondence[email protected]
&
Susana Gavidia-Payne RMIT University, Melbourne, Australia
Pages 153-162 | Published online: 10 Jul 2009

Citations (191)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (25)

Sara Bagur, Ana J. Cañas-Lerma, Bartomeu Mut-Amengual & Sebastià Verger. (2023) The impact of family characteristics on the level of empowerment and the level of Family Quality of Life of parents using Early Childhood Intervention services. International Journal of Developmental Disabilities 0:0, pages 1-10.
Read now
Rhett M. Billen, Juli Sams & Vey M. Nordquist. (2023) A conceptual model of parenting children with disabilities. Journal of Family Studies 29:4, pages 1781-1803.
Read now
Siméon T. A. Lahaije, Jorien Luijkx, Aly Waninge & Annette A. J. van der Putten. (2023) Support needs of families with a child with profound intellectual and multiple disabilities. International Journal of Developmental Disabilities 0:0, pages 1-14.
Read now
Ketty M. Sarouphim & Sara Kassem. (2022) Use of the portage curriculum to impact child and parent outcome in an early intervention program in Lebanon. Early Years 42:4-5, pages 528-542.
Read now
Thomas L. Boehm. (2022) A Flourishing Quality of Life Amidst Disability. Journal of Disability & Religion 26:4, pages 363-389.
Read now
Ester Herrera, Sofia Baena, Victoria Hidalgo & Eva Trigo. (2022) The relationship between family quality of life, mindful attention, and social support in families of people with autism spectrum disorder. International Journal of Developmental Disabilities 0:0, pages 1-11.
Read now
Karen Sagun, Alyssa Albarillo, Jethro Karl Amancio, Janessa Bulanadi, Izabella De Guzman, Vinzes Paul Jugueta & Krystin Elda Santos. (2022) Outcomes of Early Detection and Intervention of Children with Disability: Perspectives from Philippine Public School Teachers and Administrators. International Journal of Disability, Development and Education 69:4, pages 1151-1167.
Read now
Joanna Butchart, Reema Harrison, Jan Ritchie, Felip Martí, Chris McCarthy, Sarah Knight & Adam Scheinberg. (2021) Child and parent perceptions of acceptability and therapeutic value of a socially assistive robot used during pediatric rehabilitation. Disability and Rehabilitation 43:2, pages 163-170.
Read now
Karma Jigyel, Judith A. Miller, Sofia Mavropoulou & Jeanette Berman. (2020) Benefits and concerns: parents’ perceptions of inclusive schooling for children with special educational needs (SEN) in Bhutan. International Journal of Inclusive Education 24:10, pages 1064-1080.
Read now
Anoo Bhopti, Primrose Lentin & Ted Brown. (2020) Relationships between early childhood intervention services, family quality of life and parent occupations: A mixed-methods Australian study. Journal of Occupational Therapy, Schools, & Early Intervention 13:2, pages 103-125.
Read now
Jorien Luijkx, Annette A. J. van der Putten & Carla Vlaskamp. (2019) A valuable burden? The impact of children with profound intellectual and multiple disabilities on family life. Journal of Intellectual & Developmental Disability 44:2, pages 184-189.
Read now
Barbara B. Demchick, Julia Ehler, Shelly Marramar, Alison Mills & Amanda Nuneviller. (2019) Family Quality of Life When Raising a Child with Pediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcal Infection (PANDAS). Journal of Occupational Therapy, Schools, & Early Intervention 12:2, pages 182-199.
Read now
Jodie Armstrong, Katie Paskal, Catherine Elliott, John Wray, Emma Davidson, Joanne Mizen & Sonya Girdler. (2019) What makes playgroups therapeutic? A scoping review to identify the active ingredients of therapeutic and supported playgroups. Scandinavian Journal of Occupational Therapy 26:2, pages 81-102.
Read now
Cynthia Teo, Ann Kennedy-Behr & John Lowe. (2018) Contrasting perspectives of parents and service providers on respite care in Queensland, Australia. Disability & Society 33:9, pages 1503-1527.
Read now
Dawn Adams, Louise Handley, Doug Simkiss, Emily Walls, Alison Jones, Martin Knapp, Renee Romeo & Chris Oliver. (2018) Service use and access in young children with an intellectual disability or global developmental delay: Associations with challenging behaviour. Journal of Intellectual & Developmental Disability 43:2, pages 232-241.
Read now
Paola Corsano, Alessandro Musetti, Laura Guidotti & Francesca Capelli. (2017) Typically developing adolescents’ experience of growing up with a brother with an autism spectrum disorder. Journal of Intellectual & Developmental Disability 42:2, pages 151-161.
Read now
Nina Zuna, Marta Gràcia, Samuel H. Haring & Jeannie M. Aguilar. (2016) Parental perceptions and satisfaction with family services in families of children with autism spectrum disorder and other developmental disabilities. Journal of Intellectual & Developmental Disability 41:3, pages 233-242.
Read now
Iris Manor-Binyamini. (2016) Positive aspects of coping among mothers of adolescent children with developmental disability in the Druze community in Israel. Journal of Intellectual & Developmental Disability 41:2, pages 97-106.
Read now
Amanda Howard, Tamara Blakemore, Lou Johnston, Darleen Taylor & Rani Dibley. (2015) ‘I’m not really sure but I hope it’s better’: early thoughts of parents and carers in a regional trial site for the Australian National Disability Insurance Scheme. Disability & Society 30:9, pages 1365-1381.
Read now
Susana Gavidia-Payne, Katherine Meddis & Nicole Mahar. (2015) Correlates of child and family outcomes in an Australian community-based early childhood intervention program. Journal of Intellectual & Developmental Disability 40:1, pages 57-67.
Read now
Elizabeth K. Cridland, Sandra C. Jones, Peter Caputi & Christopher A. Magee. (2015) Qualitative research with families living with autism spectrum disorder: Recommendations for conducting semistructured interviews. Journal of Intellectual & Developmental Disability 40:1, pages 78-91.
Read now
Nihad A. Almasri, Maysoun Saleh & Carl J. Dunst. (2014) Psychometric properties of the Arabic Family Support Scale for families of children and youth with cerebral palsy in Jordan. Journal of Intellectual & Developmental Disability 39:3, pages 223-232.
Read now
Carina Chaij, Meekyung Han & Lisa Graziano. (2014) Latino Families with a Child with Prader–Willi Syndrome: Exploring Needs for Support. Journal of Social Work in Disability & Rehabilitation 13:3, pages 207-225.
Read now
Elizabeth K. Cridland, Peter Caputi, Sandra C. Jones & Christopher A. Magee. (2014) Understanding high-functioning autism during adolescence: A personal construct theory approach. Journal of Intellectual & Developmental Disability 39:1, pages 108-118.
Read now
JohnG. Orme, DonnaJ. Cherry & TaylorE. Krcek. (2013) Who Is Willing to Foster Children With Disabilities?. Journal of Public Child Welfare 7:5, pages 566-585.
Read now

Articles from other publishers (166)

Eline N. Desimpelaere, Bart Soenens, Peter Prinzie, Joachim Waterschoot, Maarten Vansteenkiste, Sofie Morbée, Charlotte Schrooyen & Sarah S. W. De Pauw. (2023) Parents’ Stress, Parental Burnout, and Parenting Behavior during the COVID-19 Pandemic: Comparing Parents of Children with and without Complex Care Needs. Journal of Child and Family Studies 32:12, pages 3681-3696.
Crossref
Ayelet Gur, Tali‐Noy Hindi & Lilach Krisi‐Kadosh. (2023) Family leadership among Israeli families of children with disabilities during the 2019 coronavirus disease pandemic. Child & Family Social Work.
Crossref
Carmen T. Francisco Mora, Alba Ibáñez-García & Anna Balcells-Balcells. (2023) Participants’ Bias in Disability Research on Family Quality of Life during the 0–6 Years Stage. Behavioral Sciences 13:9, pages 753.
Crossref
Thamires Rosa dos Santos, Nicoly Stefani Sevalho Carlucci, Lucimar Retto da Silva de Avó, Ingrid Tremel Barbato, Louise Lapagesse de Camargo Pinto, Rui Fernando Pilotto, Carla Maria Ramos Germano & Débora Gusmão Melo. (2023) Quality of life of Brazilian families who have children with Fragile X syndrome: a descriptive study. Journal of Community Genetics 14:4, pages 407-418.
Crossref
Andrew W. Y. Cheng & Cynthia Y. Y. Lai. (2023) Parental stress in families of children with special educational needs: a systematic review. Frontiers in Psychiatry 14.
Crossref
Bethan Collins, Nicole Anneke McGrath & Sabine Maguire. (2023) What can a Family Liaison Service offer families of children with disabilities and/or developmental difficulties?. Tizard Learning Disability Review 28:1/2, pages 33-41.
Crossref
Jagritee Singh, S. Haque Nizamie, Narendra Kumar Singh & Dipanjan Bhattacharjee. (2023) Family Stress and Dyadic Adjustment among Parents of Children with Intellectual Disability and Functional Psychosis: A Comparative Study. Eastern Journal of Psychiatry 20:1, pages 27-34.
Crossref
Siméon T. A. Lahaije, Jorien Luijkx, Aly Waninge & Annette A. J. van der Putten. (2023) Well-Being of Families with a Child with Profound Intellectual and Multiple Disabilities. Research and Practice for Persons with Severe Disabilities 48:2, pages 63-78.
Crossref
Vassilios Argyropoulos & Katerina Riga. (2023) Personal needs of parents who raise children with blindness or visual impairment. British Journal of Visual Impairment, pages 026461962311705.
Crossref
Vyda Mamley Hervie. (2023) Social inclusion of children with intellectual disabilities in Accra, Ghana: Views of parents/guardians and teachers. Children and Youth Services Review 147, pages 106845.
Crossref
Özlem EKİZOĞLU & Seyhan HASIRCI. (2023) Otizm Spektrum Bozukluğuna Sahip Çocukları Olan Annelerin Sosyal Destek Algısının, Yaşam Kalitesine EtkisiThe Effect of Social Support Perception of Mothers with Children with Autism Spectrum Disorder on Quality of Life. Akdeniz Spor Bilimleri Dergisi 6:1, pages 13-26.
Crossref
Sohyun An Kim. (2022) Transition to Kindergarten for Children on the Autism Spectrum: Perspectives of Korean–American Parents. Journal of Autism and Developmental Disorders 53:3, pages 1130-1145.
Crossref
Marija ČolićR.R. & Marko BuljevacM.M.. (2023) Formal and informal support for Croatian and Serbian people with disabilities and their families: A scoping review. Specijalna edukacija i rehabilitacija 22:4, pages 327-349.
Crossref
Jelena PetrovićR.R., Jelena ZorićM.M. & Mirjana Petrović-LazićD.D.. (2023) The relationship of sensory processing of children with developmental dysphasia with burnout and self-esteem of parents. Specijalna edukacija i rehabilitacija 22:3, pages 221-242.
Crossref
Bianca Beraldo dos Reis Valverde, Andrea Perosa Saigh Jurdi & Ana Paula da Silva Pereira. (2023) Family Benefits of Early Intervention: A Scoping Review. Psicologia: Teoria e Pesquisa 39.
Crossref
Natallia Bahdanovich Hanssen, Stefanija Ališauskienė & Daiva Kairienė. 2023. Interprofessional and Family-Professional Collaboration for Inclusive Early Childhood Education and Care. Interprofessional and Family-Professional Collaboration for Inclusive Early Childhood Education and Care 29 42 .
Songtian Zeng, Lynn Yuan, Yujin Lee, Yiyang Guan, Katherine Volk, Margaret O’Riordan & Angela K. Stone-MacDonald. 2023. Handbook of Clinical Child Psychology. Handbook of Clinical Child Psychology 137 154 .
Fina Ferrer Vidal, Rosa Vilaseca Momplet & Rosa María Bersabé. (2022) Relationship between parental perceptions, family income and support received with family quality of life in families with a child with an intellectual disability. Siglo Cero Revista Española sobre Discapacidad Intelectual 53:4, pages 89-108.
Crossref
Shengli Cheng, Sanyin Cheng, Shushan Liu & Yun Li. (2022) Parents' pandemic stress, parental involvement, and family quality of life for children with autism. Frontiers in Public Health 10.
Crossref
Ghaleb H. Alnahdi, Arwa Alwadei, Flora Woltran & Susanne Schwab. (2022) Measuring Family Quality of Life: Scoping Review of the Available Scales and Future Directions. International Journal of Environmental Research and Public Health 19:23, pages 15473.
Crossref
Sara Bagur, Berta Paz‐Lourido, Bartomeu Mut‐Amengual & Sebastià Verger. (2022) Relationship between parental mental health and developmental disorders in early childhood. Health & Social Care in the Community 30:6.
Crossref
Laura J. Dilly & Alexis Pavlov. (2022) Assessing students in foster care for autism spectrum disorders. Psychology in the Schools 59:7, pages 1402-1418.
Crossref
Ayelet Gur & Tali-Noy Hindi. (2022) Exploring fathers' perspectives on family-centered services for families of children with disabilities. Research in Developmental Disabilities 124, pages 104199.
Crossref
Christelle Vernhet, Cécile Michelon, Florine Dellapiazza, Cécile Rattaz, Marie-Maude Geoffray, Herbert Roeyers, Marie-Christine Picot, Amaria Baghdadli, Amaria Baghdadli, Catherine Chabaux, Clarisse Chatel, David Cohen, Emmanuel Damville, Marie-Maude Geoffray, Ludovic Gicquel, Renaud Jardri, Thierry Maffre, Alexandre Novo, Roxane Roxane, Marie-Joëlle Oreve, Didier Périsse, François Poinso, Julien Pottelette, Laurence Robel, Catherine Rolland, Marie Schoenberger, Sandrine Sonié, Mario Speranza & Stéphanie Vespérini. (2021) Perceptions of parents of the impact of autism spectrum disorder on their quality of life and correlates: comparison between mothers and fathers. Quality of Life Research 31:5, pages 1499-1508.
Crossref
Vesna VučinićJ.J., Valentina MartaćI.I. & Marija AnđelkovićM.M.. (2022) Family and friends' expected support to parents of children with disabilities. Specijalna edukacija i rehabilitacija 21:2, pages 117-132.
Crossref
Elaine McCarthy & Suzanne Guerin. (2021) Family‐centred care in early intervention: A systematic review of the processes and outcomes of family‐centred care and impacting factors. Child: Care, Health and Development 48:1, pages 1-32.
Crossref
Louisa Ammann-Schnell, Samuel Groeschel, Christiane Kehrer, Saskia Frölich & Ingeborg Krägeloh-Mann. (2021) The impact of severe rare chronic neurological disease in childhood on the quality of life of families—a study on MLD and PCH2. Orphanet Journal of Rare Diseases 16:1.
Crossref
Katarina Smejda Kjærandsen, Per Håkan Brøndbo & Marianne Berg Halvorsen. (2021) Determinants of caregiver satisfaction with child neurodevelopmental assessment in neuropaediatric clinics. BMC Health Services Research 21:1.
Crossref
Olha Stoliaryk. (2021) The impact of strength-based interventions on the mobility of families raising children with autism. Scientific bulletin of South Ukrainian National Pedagogical University named after K D Ushynsky 2021:3 (136), pages 96-103.
Crossref
Julia Jansen-van Vuuren, Rosemary Lysaght, Beata Batorowicz, Solomon Dawud & Heather Michelle Aldersey. (2021) Family Quality of Life and Support: Perceptions of Family Members of Children with Disabilities in Ethiopia. Disabilities 1:3, pages 233-256.
Crossref
P. Embregts, L. Heerkens, N. Frielink, S. Giesbers, L. Vromans & A. Jahoda. (2021) Experiences of mothers caring for a child with an intellectual disability during the COVID‐19 pandemic in the Netherlands. Journal of Intellectual Disability Research 65:8, pages 760-771.
Crossref
Songtian Zeng, Hongxia Zhao, Xiaoyi Hu, James D. Lee, Angela K. Stone-MacDonald & Zachary W. Price. (2020) Are we on the Same Page: a DyadicAnalysis of Parental Stress, Support, and Family Quality of Life on Raising Children with Autism Spectrum Disorders. Journal of Developmental and Physical Disabilities 33:4, pages 599-618.
Crossref
N. Luitwieler, J. Luijkx, M. Salavati, C.P. Van der Schans, A.J. Van der Putten & A. Waninge. (2021) Variables related to the quality of life of families that have a child with severe to profound intellectual disabilities: A systematic review. Heliyon 7:7, pages e07372.
Crossref
Emma Langley, Vasiliki Totsika, Richard P. Hastings & Tom Bailey. (2021) Family Relationships and Their Associations With Perceptions of Family Functioning in Mothers of Children With Intellectual Disability. American Journal on Intellectual and Developmental Disabilities 126:3, pages 187-202.
Crossref
Sebastià Verger, Inmaculada Riquelme, Sara Bagur & Berta Paz-Lourido. (2021) Satisfaction and Quality of Life of Families Participating in Two Different Early Intervention Models in the Same Context: A Mixed Methods Study. Frontiers in Psychology 12.
Crossref
İpek GÜLSÜN & Atilla CAVKAYTAR. (2021) ZİHİNSEL YETERSİZLİĞİ OLAN ÇOCUĞA SAHİP AİLELERİN YAŞAM KALİTESİ ALGILARINA İLİŞKİN ARAŞTIRMALARIN SİSTEMATİK DERLEME İLE İNCELENMESİ. Uludağ Üniversitesi Eğitim Fakültesi Dergisi.
Crossref
Elise J. Matthews, Jan Gelech, Raissa Graumans, Michel Desjardins & Isabelle Gélinas. (2020) Mediating a Fragmented System: Partnership Experiences of Parents of Children with Neurodevelopmental and Neuromuscular Disabilities. Journal of Developmental and Physical Disabilities 33:2, pages 311-330.
Crossref
Maria Villaescusa, Natxo Martínez-Rueda & Almudena Fernández. (2021) Support for Families of Youths and Adults with Intellectual Disabilities: Contributions of a Program from Families’ and Specialists’ Perspectives. Education Sciences 11:2, pages 88.
Crossref
Pau García-Grau, R. A. McWilliam, Gabriel Martínez-Rico & Catalina P. Morales-Murillo. (2019) Rasch Analysis of the Families in Early Intervention Quality of Life (FEIQoL) Scale. Applied Research in Quality of Life 16:1, pages 383-399.
Crossref
Olha Stoliaryk, Olha Zubchyk & Tetyana Semigina. (2020) Family social work: the realities of Ukraine. Scientific bulletin of South Ukrainian National Pedagogical University named after K D Ushynsky 2020:4 (133), pages 38-46.
Crossref
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.
Crossref
Kimberly Goodspeed, Geraldine Bliss & Diane Linnehan. (2020) Bringing everyone to the table – findings from the 2018 Phelan-McDermid Syndrome Foundation International Conference. Orphanet Journal of Rare Diseases 15:1.
Crossref
Julie E Sutton, Jaci C Huws & Christopher R Burton. (2019) Sleep hygiene education and children with developmental disabilities: Findings from a co-design study. Journal of Intellectual Disabilities 24:4, pages 522-542.
Crossref
Rie Wakimizu, Hiroshi Fujioka, Kaori Nishigaki & Akemi Matsuzawa. (2020) Quality of life and associated factors in siblings of children with severe motor and intellectual disabilities: A cross‐sectional study. Nursing & Health Sciences 22:4, pages 977-987.
Crossref
Anna Balcells-Balcells, Joana M. Mas, Natasha Baqués, Cecilia Simón & Simón García-Ventura. (2020) The Spanish Family Quality of Life Scales under and over 18 Years Old: Psychometric Properties and Families’ Perceptions. International Journal of Environmental Research and Public Health 17:21, pages 7808.
Crossref
Carmen Francisco Mora, Alba Ibáñez & Anna Balcells-Balcells. (2020) State of the Art of Family Quality of Life in Early Care and Disability: A Systematic Review. International Journal of Environmental Research and Public Health 17:19, pages 7220.
Crossref
Jane Meleady, Colette Clyne, Jessica Braham & Alan Carr. (2020) Positive contributions among parents of children on the autism spectrum: A Systematic review. Research in Autism Spectrum Disorders 78, pages 101635.
Crossref
Sung Hyun Kim, In Young Sung, Eun Jae Ko, Jieun Park & Nayoung Heo. (2020) Stress in Caregivers and Children with a Developmental Disorder Who Receive Rehabilitation. Children 7:9, pages 136.
Crossref
Emily Gardiner, Anton R. Miller & Lucyna M. Lach. (2020) Service adequacy and the relation between child behavior problems and negative family impact reported by primary caregivers of children with neurodevelopmental conditions. Research in Developmental Disabilities 104, pages 103712.
Crossref
S.‐J. Chiu, I.‐F. Lin, Y.‐T. Chou & L.‐Y. Chien. (2020) Family quality of life among Taiwanese children with developmental delay before and after early intervention. Journal of Intellectual Disability Research 64:8, pages 589-601.
Crossref
Vanessa Clarisse Fong, Emily Gardiner & Grace Iarocci. (2020) Can a combination of mental health services and ADL therapies improve quality of life in families of children with autism spectrum disorder?. Quality of Life Research 29:8, pages 2161-2170.
Crossref
Evangelia Koukouriki & Sryridon-Georgios Soulis. (2020) Self-reported Health-Related Quality of Life (HRQOL) and Anxiety Among Greek School-Age Siblings of Individuals with Autism Spectrum Disorders (ASD) in Relation to Parental Mental Health and Social Support. Journal of Autism and Developmental Disorders 50:8, pages 2913-2930.
Crossref
Olha Stoliaryk. (2020) Social support strategies targeted at the families raising children with autism. Scientific bulletin of South Ukrainian National Pedagogical University named after K D Ushynsky 2020:2 (131), pages 45-51.
Crossref
M. Seymour, R. Giallo & C. E. Wood. (2019) Perceptions of social support: comparisons between fathers of children with autism spectrum disorder and fathers of children without developmental disabilities. Journal of Intellectual Disability Research 64:6, pages 414-425.
Crossref
Catharine Lory, Rose A. Mason, John L. Davis, Danni Wang, So Yeon Kim, Emily Gregori & Marie David. (2020) A Meta-analysis of Challenging Behavior Interventions for Students with Developmental Disabilities in Inclusive School Settings. Journal of Autism and Developmental Disorders 50:4, pages 1221-1237.
Crossref
Katie Ekberg, Carly Meyer, Louise Hickson & Nerina Scarinci. (2020) Parents’ questions to clinicians within paediatric hearing habilitation appointments for children with hearing impairment. Patient Education and Counseling 103:3, pages 491-499.
Crossref
Janice E. Kilburn & Cheri J. Shapiro. (2018) The Structure and Function of Social Networks of Mothers of Young Children With Disabilities. Topics in Early Childhood Special Education 39:4, pages 250-259.
Crossref
Sanja DimoskiM.M. & Aleksandra GrbovićB.B.. (2020) Depression in parents of children with disability. Specijalna edukacija i rehabilitacija 19:2, pages 123-144.
Crossref
Hsiao-Yu Hsieh, Ling-Yu Chen, Kuang-Ling Ko, Hsiu-Hsiang Liu, Wen-Jiun Chou, Miao-Chun Chou, Ching-Shu Tsai & Liang-Jen Wang. (2020) Adjunctive sensory integration therapy for children with developmental disabilities in a family-based early intervention program. Taiwanese Journal of Psychiatry 34:3, pages 121.
Crossref
Nadezda Kovalcíkova, Andrea Banovcinova & Jana Levicka. (2020) The usefulness of community support resources from the perspective of parents of children with disabilities. SHS Web of Conferences 85, pages 02007.
Crossref
Songtian Zeng, Xiaoyi Hu, Hongxia Zhao & Angela K Stone-MacDonald. (2020) Examining the relationships of parental stress, family support and family quality of life: A structural equation modeling approach. Research in Developmental Disabilities 96, pages 103523.
Crossref
Ira Glovinsky & Nina Newman. 2020. Autism 360°. Autism 360° 141 160 .
Lien Vanderkerken, Mieke Heyvaert, Patrick Onghena & Bea Maes. (2019) The Relation Between Family Quality of Life and the Family‐Centered Approach in Families With Children With an Intellectual Disability. Journal of Policy and Practice in Intellectual Disabilities 16:4, pages 296-311.
Crossref
Lucía Oñate & Esther Calvete. (2019) The moderating role of age in the relationship between different stressors and the quality of life of the relatives of people with intellectual disabilities. Quality of Life Research 28:11, pages 2969-2978.
Crossref
Carolyn H. Hughes-Scholes & Susana Gavidia-Payne. (2019) Early Childhood Intervention Program Quality: Examining Family-Centered Practice, Parental Self-Efficacy and Child and Family Outcomes. Early Childhood Education Journal 47:6, pages 719-729.
Crossref
Gulser Senses Dinc, Esra Cop, Tulay Tos, Eyup Sari & Saliha Senel. (2019) Mothers of 0–3‐year‐old children with Down syndrome: Effects on quality of life. Pediatrics International 61:9, pages 865-871.
Crossref
Scott A. Sabella & Christopher S. Suchan. (2019) The Contribution of Social Support, Professional Support, and Financial Hardship to Family Caregiver Life Satisfaction After Traumatic Brain Injury. Journal of Head Trauma Rehabilitation 34:4, pages 233-240.
Crossref
Érica Bueno Camargo de Oliveira, Rafaela Catelan Martins Pereira, Aline Apis, Carla Maria Ramos Germano, Rui Fernando Pilotto & Débora Gusmão Melo. (2019) Qualidade de vida de famílias de filhos com deficiência intelectual moderada. Jornal Brasileiro de Psiquiatria 68:2, pages 101-109.
Crossref
Beth A. Currier, Maria A. Jones & Beth W. DeGrace. (2019) Experiences of Families With Young Power Wheelchair Users. Journal of Early Intervention 41:2, pages 125-140.
Crossref
Michael D. Hannon, Raymond Blanchard & Cassandra A. Storlie. (2019) Microaggression Experiences of Fathers With Children With Autism Spectrum Disorder. The Family Journal 27:2, pages 199-208.
Crossref
Thomas L. BoehmErik W. Carter. (2019) Family Quality of Life and Its Correlates Among Parents of Children and Adults With Intellectual Disability. American Journal on Intellectual and Developmental Disabilities 124:2, pages 99-115.
Crossref
Pau García-Grau, R. A. McWilliam, Gabriel Martínez-Rico & Catalina P. Morales-Murillo. (2018) Child, Family, and Early Intervention Characteristics Related to Family Quality of Life in Spain. Journal of Early Intervention 41:1, pages 44-61.
Crossref
Cila Umat, Nor Haniza Abdul Wahat, Sakinah Che Ross & Bee See Goh. (2019) Quality of life of parents and siblings of children with cochlear implants. Journal of Otology 14:1, pages 17-21.
Crossref
Anna Balcells-Balcells, Climent Giné, Joan Guàrdia-Olmos, Jean Ann Summers & Joana M. Mas. (2019) Impact of supports and partnership on family quality of life. Research in Developmental Disabilities 85, pages 50-60.
Crossref
Aurélie Chaume, Jennifer Ilg & Céline Clément. (2020) Comparaison de la qualité de vie familiale de parents français ayant ou non un enfant avec un trouble du spectre de l’autisme. Revue francophone de la déficience intellectuelle 29, pages 36-45.
Crossref
Mindy Scheithauer, Colin Muething, Kristina R. Gerencser & Nathan A. Call. 2019. Handbook of Intellectual Disabilities. Handbook of Intellectual Disabilities 583 605 .
Raquel Alveirinho Correia & Maria João Seabra-Santos. (2018) Qualidade de Vida Familiar na Deficiência Intelectual: Revisão Sistemática de Estudos. Psicologia: Teoria e Pesquisa 34:0.
Crossref
Christene J. Louw, Hermanus B. Grobler & Richard G. Cowden. (2018) Strengthening intellectually challenged adolescents’ sense of self: An appreciative inquiry mixed-methods intervention. Health SA Gesondheid 23.
Crossref
E. Gardiner, A. R. Miller & L. M. Lach. (2018) Family impact of childhood neurodevelopmental disability: considering adaptive and maladaptive behaviour. Journal of Intellectual Disability Research 62:10, pages 888-899.
Crossref
Katie Ekberg, Nerina Scarinci, Louise Hickson & Carly Meyer. (2018) Parent-directed commentaries during children's hearing habilitation appointments: a practice in family-centred care. International Journal of Language & Communication Disorders 53:5, pages 929-946.
Crossref
Lien Vanderkerken, Mieke Heyvaert, Patrick Onghena & Bea Maes. (2017) Quality of Life in Flemish Families with a Child with an Intellectual Disability: a Multilevel Study on Opinions of Family Members and the Impact of Family Member and Family Characteristics. Applied Research in Quality of Life 13:3, pages 779-802.
Crossref
Monique M. Ridosh, Kathleen J. Sawin, Timothy J. Brei & Rachel F. Schiffman. (2018) A Global Family Quality of Life Scale: Preliminary psychometric evidence. Journal of Pediatric Rehabilitation Medicine 11:2, pages 103-114.
Crossref
Line Jenhaug & Ole Petter Askheim. (2018) Empowering Parents as Co-producers: Personal Assistance for Families with Disabled Children. Scandinavian Journal of Disability Research 20:1, pages 266-276.
Crossref
Emily Gardiner & Grace Iarocci. (2018) Examining Family Quality of Life Within the Context of a Participant‐Directed ASD Funding Program in British Columbia, Canada. Journal of Policy and Practice in Intellectual Disabilities 15:2, pages 110-123.
Crossref
Pau García-Grau, R. A. McWilliam, Gabriel Martínez-Rico & María D. Grau-Sevilla. (2017) Factor Structure and Internal Consistency of a Spanish Version of the Family Quality of Life (FaQoL). Applied Research in Quality of Life 13:2, pages 385-398.
Crossref
Emily J Hickey, Lindsay Dubois & Sigan L Hartley. (2017) Positive and negative social exchanges experienced by fathers and mothers of children with autism. Autism 22:4, pages 469-478.
Crossref
Yun‐Ju Hsiao. (2018) Autism Spectrum Disorders: Family Demographics, Parental Stress, and Family Quality of Life. Journal of Policy and Practice in Intellectual Disabilities 15:1, pages 70-79.
Crossref
Karen Goldrich Eskow, Jean Ann Summers, Gregory S. Chasson & Renae Mitchell. (2018) The Association Between Family–Teacher Partnership Satisfaction and Outcomes of Academic Progress and Quality of Life for Children/Youth With Autism. Journal of Policy and Practice in Intellectual Disabilities 15:1, pages 16-25.
Crossref
Helen Bourke-Taylor, Claire Cotter, Lindy Johnson & Aislinn Lalor. (2018) Belonging, school support and communication: Essential aspects of school success for students with cerebral palsy in mainstream schools. Teaching and Teacher Education 70, pages 153-164.
Crossref
Babita Prusty. 2018. Autism Spectrum Disorders. Autism Spectrum Disorders 60 87 .
Niels Ove Illum, Mette Bonderup & Kim Oren Gradel. (2018) Parents’ Expressions of Concerns and Hopes for the Future and Their Concomitant Assessments of Disability in Their Children. Clinical Medicine Insights: Pediatrics 12, pages 117955651878494.
Crossref
Yasamine Bolourian & Jan Blacher. 2018. 181 212 .
Joanna E. Lomas Mevers, Nathan A. Call & Sarah J. Miller. (2017) Practice Recommendations for Addressing Problem Behaviors in Siblings with Autism Spectrum Disorder. Behavior Analysis in Practice 10:4, pages 363-374.
Crossref
Yun-Ju Hsiao, Kyle Higgins, Tom Pierce, Peggy J. Schaefer Whitby & Richard D. Tandy. (2017) Parental stress, family quality of life, and family-teacher partnerships: Families of children with autism spectrum disorder. Research in Developmental Disabilities 70, pages 152-162.
Crossref
Carl J. Dunst. (2017) Research Foundations for Evidence-Informed Early Childhood Intervention Performance Checklists. Education Sciences 7:4, pages 78.
Crossref
Nicole Edwards, Julie King, Hanna Watling & Sara Amy Hair. (2017) Qualitative exploration of psychotropic medication to manage challenging behaviour in adults with intellectual disability: views of family members. Advances in Mental Health and Intellectual Disabilities 11:5/6, pages 207-218.
Crossref
Jan Pieter Marchal, Hedy A. van Oers, Heleen Maurice-Stam, Martha A. Grootenhuis, A.S. Paul van Trotsenburg & Lotte Haverman. (2017) Distress and everyday problems in Dutch mothers and fathers of young adolescents with Down syndrome. Research in Developmental Disabilities 67, pages 19-27.
Crossref
Femke Boelsma, Irene Caubo-Damen, Alice Schippers, Menco Dane & Tineke A. Abma. (2017) Rethinking FQoL: The Dynamic Interplay Between Individual and Family Quality of Life. Journal of Policy and Practice in Intellectual Disabilities 14:1, pages 31-38.
Crossref
Fina Ferrer, Rosa Vilaseca & Joan Guàrdia Olmos. (2016) Positive perceptions and perceived control in families with children with intellectual disabilities: relationship to family quality of life. Quality & Quantity 51:2, pages 903-918.
Crossref
Sean Jones, Emily Bremer & Meghann Lloyd. (2016) Autism spectrum disorder: family quality of life while waiting for intervention services. Quality of Life Research 26:2, pages 331-342.
Crossref
S. Hodgetts, D. McConnell, L. Zwaigenbaum & D. Nicholas. (2017) The impact of autism services on mothers' psychological wellbeing. Child: Care, Health and Development 43:1, pages 18-30.
Crossref
Nathan A. Call, Mindy C. Scheithauer & Joanna Lomas Mevers. 2017. Applied Behavior Analysis Advanced Guidebook. Applied Behavior Analysis Advanced Guidebook 41 71 .
Henrik Friberg-FernrosHenrik Friberg-Fernros. 2017. Making a Case for Stricter Abortion Laws. Making a Case for Stricter Abortion Laws 55 93 .
Anoo Bhopti, Ted Brown & Primrose Lentin. (2016) Family Quality of Life. Journal of Early Intervention 38:4, pages 191-211.
Crossref
Celia C. Y. Wong, Winnie W. S. Mak & Kelly Yu-Hsin Liao. (2016) Self-Compassion: a Potential Buffer Against Affiliate Stigma Experienced by Parents of Children with Autism Spectrum Disorders. Mindfulness 7:6, pages 1385-1395.
Crossref
Fina Ferrer, Rosa Vilaseca & Rosa Maria Bersabé. (2016) The Impact of Demographic Characteristics and the Positive Perceptions of Parents on Quality of Life in Families with a Member with Intellectual Disability. Journal of Developmental and Physical Disabilities 28:6, pages 871-888.
Crossref
Monique M. Ridosh, Kathleen J. Sawin, Rachel F. Schiffman & Bonnie P. Klein-Tasman. (2016) Factors associated with parent depressive symptoms and family quality of life in parents of adolescents and young adults with and without Spina Bifida. Journal of Pediatric Rehabilitation Medicine 9:4, pages 287-302.
Crossref
Judith McKenzie & Roy McConkey. (2016) Caring for Adults with Intellectual Disability: The Perspectives of Family Carers in South Africa. Journal of Applied Research in Intellectual Disabilities 29:6, pages 531-541.
Crossref
Clarissa Altina Cunha de Araújo, Berta Paz-Lourido & Sebastià Verger Gelabert. (2016) Tipos de apoyo a las familias con hijos con discapacidad y su influencia en la calidad de vida familiar. Ciência & Saúde Coletiva 21:10, pages 3121-3130.
Crossref
Kathleen B. Kyzar, Sara E. Brady, Jean Ann Summers, Shana J. Haines & Ann P. Turnbull. (2016) Services and Supports, Partnership, and Family Quality of Life. Exceptional Children 83:1, pages 77-91.
Crossref
Joana Maria Mas, Climent Giné & Robin A. McWilliam. (2016) The Adaptation Process of Families With Children With Intellectual Disabilities in Catalonia. Infants & Young Children 29:4, pages 335-351.
Crossref
Thomas L. Boehm & Erik W. Carter. (2016) A Systematic Review of Informal Relationships Among Parents of Individuals With Intellectual Disability or Autism. Research and Practice for Persons with Severe Disabilities 41:3, pages 173-190.
Crossref
Elizabeth K. Cridland, Sandra C. Jones, Gerard Stoyles, Peter Caputi & Christopher A. Magee. (2016) Families Living With Autism Spectrum Disorder. Focus on Autism and Other Developmental Disabilities 31:3, pages 196-207.
Crossref
Mitchell Schertz, Yael Karni-Visel, Ada Tamir, Jacob Genizi & Dana Roth. (2016) Family quality of life among families with a child who has a severe neurodevelopmental disability: Impact of family and child socio-demographic factors. Research in Developmental Disabilities 53-54, pages 95-106.
Crossref
Yasamine Bolourian & Jan Blacher. (2016) Impact of Youth with Intellectual and Developmental Disabilities on Families: Balancing Perspectives. Current Developmental Disorders Reports 3:2, pages 116-123.
Crossref
Neil James. (2015) Family carers’ experience of the need for admission of their relative with an intellectual disability to an Assessment and Treatment Unit. Journal of Intellectual Disabilities 20:1, pages 34-54.
Crossref
Joana M. Mas, Natasha Baqués, Anna Balcells-Balcells, Mariona Dalmau, Climent Giné, Marta Gràcia & Rosa Vilaseca. (2016) Family Quality of Life for Families in Early Intervention in Spain. Journal of Early Intervention 38:1, pages 59-74.
Crossref
Eleni Vasilopoulou & Joy Nisbet. (2016) The quality of life of parents of children with autism spectrum disorder: A systematic review. Research in Autism Spectrum Disorders 23, pages 36-49.
Crossref
Babita Prusty. 2016. Handbook of Research on Diagnosing, Treating, and Managing Intellectual Disabilities. Handbook of Research on Diagnosing, Treating, and Managing Intellectual Disabilities 82 108 .
Anna Balcells-Balcells, Climent Giné, Joan Guàrdia-Olmos & Jean Ann Summers. (2016) Proposal of indexes to evaluate Family Quality of Life, Partnership, and Family support needs. Revista Iberoamericana de Psicología y Salud 7:1, pages 31-40.
Crossref
Carl J. Dunst & Marilyn Espe-Sherwindt. 2016. Handbook of Early Childhood Special Education. Handbook of Early Childhood Special Education 37 55 .
Climent Giné, Marta Gràcia, Rosa Vilaseca, Francesc Salvador Beltran, Anna Balcells-Balcells, Mariona Dalmau Montalà, Ana Luisa Adam-Alcocer, Maria Teresa Pro, David Simó-Pinatella & Joana Maria Mas Mestre. (2015) Family Quality of Life for People With Intellectual Disabilities in Catalonia. Journal of Policy and Practice in Intellectual Disabilities 12:4, pages 244-254.
Crossref
Leila Dehghan, Asghar Dalvandi, Mehdi Rassafiani, Seyed Ali Hosseini, Hamid Dalvand & Sue Baptiste. (2015) Social participation experiences of mothers of children with cerebral palsy in an Iranian context. Australian Occupational Therapy Journal 62:6, pages 410-419.
Crossref
Thomas L. Boehm, Erik W. Carter & Julie Lounds Taylor. (2015) Family Quality of Life During the Transition to Adulthood for Individuals With Intellectual Disability and/or Autism Spectrum Disorders. American Journal on Intellectual and Developmental Disabilities 120:5, pages 395-411.
Crossref
Bernie Carter, Maria Edwards & Anne Hunt. (2014) ‘Being a presence’. Journal of Child Health Care 19:3, pages 304-319.
Crossref
Nara Liana Pereira-Silva, Maria Auxiliadora Dessen & Altemir José Gonçalves Barbosa. (2015) Ajustamento Conjugal: Comparação entre Casais com e sem Filhos com Deficiência Intelectual. Psico-USF 20:2, pages 297-308.
Crossref
Kitty-Rose Foley, Jenny Bourke, Stewart L. Einfeld, Bruce J. Tonge, Peter Jacoby & Helen Leonard. (2015) Patterns of Depressive Symptoms and Social Relating Behaviors Differ Over Time From Other Behavioral Domains for Young People With Down Syndrome. Medicine 94:19, pages e710.
Crossref
Nathan A. Call, Andrea R. Reavis, Courtney E. McCracken, Scott E. Gillespie & Mindy C. Scheithauer. (2014) The Impact of Delays on Parents’ Perceptions of Treatments for Problem Behavior. Journal of Autism and Developmental Disorders 45:4, pages 1013-1025.
Crossref
Gardiner Emily & Iarocci Grace. (2015) Family Quality of Life and ASD: The Role of Child Adaptive Functioning and Behavior Problems. Autism Research 8:2, pages 199-213.
Crossref
Andréa Regina Nunes Misquiatti, Maria Claudia Brito, Fernanda Terezinha Schmidtt Ferreira & Francisco Baptista Assumpção Júnior. (2015) Sobrecarga familiar e crianças com transtornos do espectro do autismo: perspectiva dos cuidadores. Revista CEFAC 17:1, pages 192-200.
Crossref
Hyunkyung Choi. (2015) Adaptation in Families of Children with Down Syndrome: A Mixed-methods Design. Journal of Korean Academy of Nursing 45:4, pages 501.
Crossref
Jessica P. Álvarez, Nathan A. Call & Joanna E. Lomas Mevers. (2014) Increasing the Social Validity of Function-Based Treatments for Problem Behavior. Acta de Investigación Psicológica 4:3, pages 1683-1700.
Crossref
Kitty-Rose Foley, Sonya Girdler, Jenny Downs, Peter Jacoby, Jenny Bourke, Nick Lennox, Stewart Einfeld, Gwynnyth Llewellyn, Trevor R. Parmenter & Helen Leonard. (2014) Relationship between family quality of life and day occupations of young people with Down syndrome. Social Psychiatry and Psychiatric Epidemiology 49:9, pages 1455-1465.
Crossref
A. LaForme Fiss, L. A. Chiarello, D. Bartlett, R. J. Palisano, L. Jeffries, N. Almasri & H-J. Chang. (2014) Family ecology of young children with cerebral palsy. Child: Care, Health and Development 40:4, pages 562-571.
Crossref
Iris Manor-Binyamini. (2014) Positive aspects of the coping of mothers of adolescent children with developmental disability in the Bedouin community in Israel. Research in Developmental Disabilities 35:6, pages 1272-1280.
Crossref
권회연 & Joonghui Park. (2014) The Trend of Study on Family Quality of Life for the Family of a Member with Disability : Based on Sub-area of FQoLS. The Journal of Inclusive Education 9:1, pages 103-133.
Crossref
N. A. Almasri, M. Saleh & C. J. Dunst. (2014) Family resources for families of children with cerebral palsy in Jordan: psychometric properties of the Arabic-Family Resources Scale. Child: Care, Health and Development 40:3, pages 354-362.
Crossref
Elizabeth K Cridland, Sandra C Jones, Christopher A Magee & Peter Caputi. (2013) Family-focused autism spectrum disorder research: A review of the utility of family systems approaches. Autism 18:3, pages 213-222.
Crossref
Jenny Ziviani, Yvonne Darlington, Rachel Feeney, Sylvia Rodger & Pauline Watter. (2014) Early intervention services of children with physical disabilities: Complexity of child and family needs. Australian Occupational Therapy Journal 61:2, pages 67-75.
Crossref
David McConnell, Amber Savage & Rhonda Breitkreuz. (2014) Resilience in families raising children with disabilities and behavior problems. Research in Developmental Disabilities 35:4, pages 833-848.
Crossref
Hayfaa Y. Al-Kandari. (2013) Parents’ and Professionals’ Perceptions of the Services of Families of Children with Intellectual Developmental Disabilities. Child and Adolescent Social Work Journal 31:2, pages 119-142.
Crossref
Karen E. Kresak, Peggy A. Gallagher & Susan J. Kelley. (2014) Grandmothers Raising Grandchildren With Disabilities. Journal of Early Intervention 36:1, pages 3-17.
Crossref
Osnat Rubin & Michal Schreiber-Divon. (2014) Mothers of Adolescents with Intellectual Disabilities: The “Meaning” of Severity Level. Psychology 05:06, pages 587-594.
Crossref
D. W. Tessier, J. L. Hefner & A. Newmeyer. (2014) Factors Related to Psychosocial Quality of Life for Children with Cerebral Palsy. International Journal of Pediatrics 2014, pages 1-6.
Crossref
Bekir Fatih Meral, Atilla Cavkaytar, Ann P. Turnbull & Mian Wang. (2013) Family Quality of Life of Turkish Families Who Have Children with Intellectual Disabilities and Autism. Research and Practice for Persons with Severe Disabilities 38:4, pages 233-246.
Crossref
Jan Pieter Marchal, Heleen Maurice-Stam, Janneke Hatzmann, A.S. Paul van Trotsenburg & Martha A. Grootenhuis. (2013) Health related quality of life in parents of six to eight year old children with Down syndrome. Research in Developmental Disabilities 34:11, pages 4239-4247.
Crossref
Songee Kim & Xinran Y. Lehto. (2013) Travel by families with children possessing disabilities: Motives and activities. Tourism Management 37, pages 13-24.
Crossref
Kristin Litzelman, Emily Barker, Kristine Catrine, Diane Puccetti, Peggy Possin & Whitney P. Witt. (2012) Socioeconomic disparities in the quality of life in children with cancer or brain tumors: the mediating role of family factors. Psycho-Oncology 22:5, pages 1081-1088.
Crossref
Laura Green. (2013) The Well-Being of Siblings of Individuals with Autism. ISRN Neurology 2013, pages 1-7.
Crossref
Neil James. (2013) The formal support experiences of family carers of people with an intellectual disability who also display challenging behaviour and/or mental health issues. Journal of Intellectual Disabilities 17:1, pages 6-23.
Crossref
Ilknur Cifci Tekinarslan. (2013) A Comparison Study of Depression and Quality of Life in Turkish Mothers of Children with down Syndrome, Cerebral Palsy, and Autism Spectrum Disorder. Psychological Reports 112:1, pages 266-287.
Crossref
Darryn Sikora, Erin Moran, Felice Orlich, Trevor A. Hall, Erica A. Kovacs, Jennifer Delahaye, Traci E. Clemons & Karen Kuhlthau. (2013) The relationship between family functioning and behavior problems in children with autism spectrum disorders. Research in Autism Spectrum Disorders 7:2, pages 307-315.
Crossref
Bianca Denny, Kathe Beyerle, Mandy Kienhuis, Ancuta Cora, Susana Gavidia‐Payne & Winita Hardikar. (2012) New insights into family functioning and quality of life after pediatric liver transplantation. Pediatric Transplantation 16:7, pages 711-715.
Crossref
Emily Gardiner & Grace Iarocci. (2012) Unhappy (and happy) in their own way: A developmental psychopathology perspective on quality of life for families living with developmental disability with and without autism. Research in Developmental Disabilities 33:6, pages 2177-2192.
Crossref
Unnur Arnadottir & Snaefridur Thora Egilson. (2012) Evaluation of therapy services with the Measure of Processes of Care (MPOC-20):. Journal of Child Health Care 16:1, pages 62-74.
Crossref
P. S. Samuel, F. Rillotta & I. Brown. (2011) Review: The development of family quality of life concepts and measures. Journal of Intellectual Disability Research 56:1, pages 1-16.
Crossref
P. S. Samuel, K. L. Hobden, B. W. LeRoy & K. K. Lacey. (2011) Analysing family service needs of typically underserved families in the USA. Journal of Intellectual Disability Research 56:1, pages 111-128.
Crossref
F. Rillotta, N. Kirby, J. Shearer & T. Nettelbeck. (2011) Family quality of life of Australian families with a member with an intellectual/developmental disability. Journal of Intellectual Disability Research 56:1, pages 71-86.
Crossref
X. Hu, M. Wang & X. Fei. (2011) Family quality of life of Chinese families of children with intellectual disabilities. Journal of Intellectual Disability Research 56:1, pages 30-44.
Crossref
S. Neikrug, D. Roth & J. Judes. (2011) Lives of quality in the face of challenge in Israel. Journal of Intellectual Disability Research 55:12, pages 1176-1184.
Crossref
R. Steel, L. Poppe, S. Vandevelde, G. Van Hove & C. Claes. (2011) Family quality of life in 25 Belgian families: quantitative and qualitative exploration of social and professional support domains. Journal of Intellectual Disability Research 55:12, pages 1123-1135.
Crossref
A. Balcells‐Balcells, C. Giné, J. Guàrdia‐Olmos & J. A. Summers. (2010) Family quality of life: adaptation to Spanish population of several family support questionnaires. Journal of Intellectual Disability Research 55:12, pages 1151-1163.
Crossref
Maria Cláudia Brito & Andréa Regina Nunes Misquiatti. (2011) Iniciativas de comunicação na interação entre crianças com distúrbios do espectro autístico e suas mães: análise pragmática. Revista CEFAC 13:6, pages 993-1001.
Crossref
Preethy S. Samuel, Karen L. Hobden & Barbara W. LeRoy. 2011. Disability and Community. Disability and Community 49 83 .
Jennifer Fereday, Candice Oster & Philip Darbyshire. (2010) Partnership in practice: what parents of a disabled child want from a generic health professional in Australia. Health & Social Care in the Community 18:6, pages 624-632.
Crossref
Fiona Rillotta, Neil Kirby & Joanne Shearer. 2011. Enhancing the Quality of Life of People with Intellectual Disabilities. Enhancing the Quality of Life of People with Intellectual Disabilities 305 348 .

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.