Results 211 to 220 of about 967,104 (403)

Young people with learning disabilities who sexually abuse: understanding, identifying and responding from within generic education and welfare services

, 2007
Rachel Fyson
openalex   +1 more source

SENSITIVITY OF PEOPLE WITH DISABILITIES: A PERSPECTIVE FROM COMMUNICATION AND RELATIONSHIP THEORY A SYSTEMATIC LITERATURE REVIEW

Sabar Riyadi, Meiti Subardhini
openalex   +2 more sources

The role of Research‐Practice Ambassadors in strengthening socially just and equitable partnership processes

American Journal of Community Psychology, EarlyView.
Abstract Research‐Practice Partnerships seek to close the research‐practice gap through developing collaborative, authentic partnerships between researchers and community members. Our team has leveraged Research‐Practice Ambassadors to support socially just and equitable partnership processes in schools.
Danielle R. Hatchimonji, Lauren McNeela, Zumana Noor, Melissa Stoffers, Tia N. Barnes, Kira Branch, Danika Perry, Amanda Parks, Mariam Berthe   +8 more
wiley   +1 more source

Equity Access: Authentic Simulations of Caring for People With Disabilities. [PDF]

Nurse Educ
Evatt M, Williams S, Henry R, Kalarchian M, Kronk R.   +4 more
europepmc   +1 more source

A Case Study On Empowering A Non-Profit Organization To Better Help People With Disabilities Through M-Health

, 2014
James P. Lawler, Hannah Moller, Robert Salloum   +2 more
openalex   +1 more source

Barriers to healthcare for people with disabilities: an umbrella review

Sara Rotenberg, Grace Jo, Hannah Kuper, Bonnielin Swenor, Franz Castro, Layla Shahbander, Varshini Varadaraj, Lori Rosman   +7 more
openalex   +1 more source

The Diagnosis That Arrived Decades Late: Living Without and Then With Myhre Syndrome

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (MIM #139210) is a rare multisystem disorder first described in 1981, characterized by short stature, neurodevelopmental delay, joint contractures, and cardiopulmonary complications. Its molecular basis, recurrent pathogenic variants in SMAD4, was not discovered until 2011. This narrative is based on a review of medical records,
Abdallah F. Elias
wiley   +1 more source

Pandemic-related experiences of older adults and people with disabilities. [PDF]

PLoS One
Mortenson WB, Esfandiari E, Mohammadi S, Sakakibara B, Schmidt J, Simpson E, Chan J, Reid H, Rash I, Brooks E, Tao G, Krahn Q, Irish J, Forwell S, Backman C, Borisoff J, Ketter N, Yu N, Miller WC.   +18 more
europepmc   +1 more source

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source

ConnectUp: Co-Designing an Online Social Connection Platform with People with Disabilities and Carers. [PDF]

Behav Sci (Basel)
Kwasnicka D, Jokovich S, Atherton C, Joy E, Mullen G, McVeigh J, Jenkinson S, Hatton J, Rogers P, Shah A, Mergelsberg E, Thompson C.   +11 more
europepmc   +1 more source