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Child: Care, Health and Development|February 21, 2009
Parent views on enhancing the quality of health care for their children with fragile X syndrome, autism or Down syndromeP Minnes, K SteinerJournal of Intellectual Disability Research : JIDR|November 17, 2005
Empowerment in parents of school-aged children with and without developmental disabilitiesJ S Nachshen, P MinnesJournal of Intellectual Disability Research : JIDR|April 29, 2016
Examining the social participation of children and adolescents with Intellectual Disabilities and Autism Spectrum Disorder in relation to peersA Taheri, A Perry, P MinnesJournal of Intellectual Disability Research : JIDR|November 21, 2017
Exploring factors that impact activity participation of children and adolescents with severe developmental disabilitiesA Taheri, A Perry, P MinnesJournal of Intellectual Disability Research : JIDR|August 30, 2014
Predictors of distress and well-being in parents of young children with developmental delays and disabilities: the importance of parent perceptionsP Minnes, A Perry, J A WeissJournal of Intellectual Disability Research : JIDR|June 6, 2003
The Family Stress and Coping Interview for families of individuals with developmental disabilities: a lifespan perspective on family adjustmentJ S Nachshen, L Woodford, P MinnesBrain Injury|December 5, 1998
A transitional living environment for persons with brain injuries: staff and client perceptionsP Minnes, L Harrick, P Carlson, et al.Brain Injury|July 1, 1994
Stability of functional outcomes following transitional living programme participation: 3-year follow-upL Harrick, L Krefting, J Johnston, et al.Brain Injury|September 2, 2000
Coping and stress in Canadian family caregivers of persons with traumatic brain injuriesP Minnes, S Graffi, M L Nolte, et al.Archives of Physical Medicine and Rehabilitation|April 11, 2001
The community integration measure: development and preliminary validationM A McColl, D Davies, P Carlson, et al.Pageof 2