Results 151 to 160 of about 624,836 (282)
Abstract This study analyzes a participatory project to develop peer support services for people with serious mental illnesses (SMIs) in China. Drawing on interviews with psychiatrists, social workers, service users, and a family caregiver, it examines the conditions, challenges, facilitators, and outcomes of participation in a paternalistic context ...
Zhiying Ma +6 more
wiley +1 more source
Reply to the Comments on 'Specific Learning Disability: Ten Challenges and Ten Recommendations in Current Indian Context'. [PDF]
Tom A +4 more
europepmc +1 more source
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 +8 more
wiley +1 more source
Interventions for children and adolescents with specific learning disability and co-occurring disorders. [PDF]
Espinas DR, Vaughn S, Fuchs LS.
europepmc +1 more source
ABSTRACT TSPEAR (chr. 21q22.3) encodes a protein involved in tooth development and is predominantly expressed in the enamel knot. Biallelic loss of function variants in TSPEAR cause ectodermal dysplasia, tooth agenesis and sensorineural hearing loss. However, the role of TSPEAR in auditory processes is unclear.
Debora Vergani +17 more
wiley +1 more source
Specific Learning Disability: Ten Challenges and Ten Recommendations in Current Indian Context. [PDF]
Tom A +4 more
europepmc +1 more source
ABSTRACT To enhance clinicians' understanding of Sifrim‐Hitz‐Weiss syndrome (SIHIWES), this study investigated the clinical phenotypes, genetic characteristics, and response to growth hormone therapy in a patient. A case of a patient with global developmental delay and distinctive facial features is presented.
Jianmei Zhang +6 more
wiley +1 more source
Specific Learning Disabilities: Issues that Remain Unanswered [PDF]
Adarsh Kohli +2 more
openaire +3 more sources
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 +6 more
wiley +1 more source
Specific learning disability — the road to disability act
Saheli, Misra, Jaydeep, Choudhury
openaire +2 more sources

