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One or more keywords matched the following properties of Msall, Michael E.
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overview For 34 years, I have been involved with understanding the complexity of child, adolescent, and adult neurodevelopmental disability and community outcomes of health, functioning, and participation. I bring expertise in qualitative and quantitative methods for modelling health status, resiliency and missed opportunities across childhood, adolescent and young adult life for individuals born prematurely. I have trained 54 postdoctoral fellows in their use of developmental and functional assessments, biomarkers, and clinical outcomes research, of which 95% have gone on to successful scientific and clinical-academic medical leadership positions. Throughout my career, I have asked the question how do individuals with prematurity at highest risk for early onset neurodevelopmental disabilities fare with respect to their long-term physical, developmental and social health outcomes? In my first U.S. academic job, I was responsible for neurodevelopmental consultative services linked to primary medical care and community care coordination (UCP, ARC, People’s Inc.) for individuals age birth to 90 years with CP and related neurodevelopmental disabilities. For these efforts, I received the Sir James Carreras International Variety Club Award. In my academic positions at Brown University and University of Chicago, I have continued to develop interdisciplinary regional management teams to promote functioning and participation for individuals with neurodevelopmental disabilities. With interdisciplinary colleagues, I developed a pediatric functional independence measure (WeeFIMTM) that has been used for 3-7 year outcomes in three NIH Multicenter Studies: Cryosurgery for Retinopathy of Prematurity (Pediatrics. 2000;106(5):998-1005. PMID: 11061766), Fetal Surgery for Myelomeningocele (Childs Nerv Syst. 2011 Jul;27(7):1083-8. PMID:21327591), and the CoolCap trial of cooling for neonatal encephalopathy (Guillet et al. Pediatr Res. 2012 Feb;71(2):205-9. PMID:22258133). More recently, I developed the Warner Initial Development Evaluation of Adaptive and Functional Skills (WIDEA-FS), which tracks emerging motor, communicative, and adaptive competencies in the first two years, and the Child Health Impairment-Functioning, Participation, and Participation (CHI-FPS) Checklist for children 7-18 years. These instruments were respectively normed on over 1500 neurotypical children and over 1500 children with disabilities. These tools were validated against specific standardized motor, communicative, developmental, psychological, and educational achievement tests. These indicators of challenges in daily activities and their impact on family life were subsequently implemented in community populations in New England, the International Rett Registry, the Western Australia Down Syndrome Registry, the U.S. and Australian Newborn Encephalopathy-Hypothermia and Erythropoietin Trials, and the Cerebral Palsy Research Registry. In all of these efforts, longitudinal strategies for tracking physical developmental and behavioral health outcomes, as well as functioning, participation and individual and family well-being occurred through interdisciplinary teams of health and rehabilitation professionals committed to enablement.
One or more keywords matched the following items that are connected to Msall, Michael E.
Item TypeName
Concept Family
Concept Family Relations
Concept Family Characteristics
Concept Family Health
Concept Professional-Family Relations
Academic Article Measuring functional status and family support in older school-aged children with cerebral palsy: comparison of three instruments.
Academic Article Functional limitations and key indicators of well-being in children with disability.
Academic Article Physical and mental health of mothers caring for a child with Rett syndrome.
Academic Article Physical and mental health in mothers of children with Down syndrome.
Academic Article Establishing a translational science for autistic spectrum disorders for children and their families: optimizing function, participation, and well-being.
Academic Article Family needs and profiles for children with cerebral palsy: understanding supports in times of scarcity.
Academic Article Family developmental risk factors among adolescents with disabilities and children of parents with disabilities.
Academic Article Child and adult disability in the 2000 Census: disability is a household affair.
Academic Article Neurodevelopmental management strategies for children with cerebral palsy: optimizing function, promoting participation, and supporting families.
Academic Article Disparities in adversity among children with autism spectrum disorder: a population-based study.
Academic Article Children with developmental disabilities experience higher levels of adversity.
Grant Leadership Education in Neurodevelopmental Disabilities in Illinois
Academic Article Establishing community pathways for the early recognition of cerebral palsy: red flags, enablement, and family support.
Academic Article Late adolescent & young adult functioning and participation outcomes after prematurity.
Academic Article Family Reflections on a Lifecourse Journey after Neonatal Intensive Care: Neurodiversity, Enablement and Hope.
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