Results 81 to 90 of about 516,293 (412)
50 Years of Disability as a National Priority [PDF]
, 2011 https://digitalcommons.usu.edu/cpd_blog/1447/thumbnail ...
Center for Persons With Disabilities
core +1 more source
Sustainable Development, 2018 Consistently, it has been reported that persons with disabilities face multiple challenges in societies and thus it is important that deliberate intervention programs are initiated to empower them to overcome exclusion.
M. Opoku +4 more
semanticscholar +1 more source
INF2‐Related Charcot–Marie–Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background INF2 mutations cause focal segmental glomerulosclerosis (FSGS) and Charcot–Marie–Tooth disease (CMT). Accurate genetic diagnosis is critical, as INF2‐related FSGS is typically resistant to immunotherapy yet rarely recurs after transplantation, and its associated neuropathy can mimic treatable immune‐mediated disorders such as ...
Chikashi Yano +27 more
wiley +1 more source
Use of Personal Listening Devices Among College Students in India During the COVID-19 Pandemic
Online Journal of Health & Allied Sciences, 2022 Objective: The objective of the study was to understand the college students' knowledge practices, and preferences regarding the use of Personal Listening Devices (PLDs) during the Covid-19 pandemic.
Balambigai N +3 more
doaj
Brown Bag Discussion: CPD\u27s ASD Interdisciplinary Clinic [PDF]
, 2011 https://digitalcommons.usu.edu/cpd_blog/1435/thumbnail ...
Center for Persons With Disabilities
core +1 more source
Access to health care for persons with disabilities in rural South Africa
BMC Health Services Research, 2017 BackgroundGlobal research suggests that persons with disabilities face barriers when accessing health care services. Yet, information regarding the nature of these barriers, especially in low-income and middle-income countries is sparse.
R. Vergunst +11 more
semanticscholar +1 more source
Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco +18 more
wiley +1 more source
Frontiers in Computational Neuroscience, 2014 We propose a mini-max feedback control (MMFC) model as a robust approach to human motor control under conditions of uncertain dynamics, such as structural uncertainty. The MMFC model is an expansion of the optimal feedback control (OFC) model.
Yuki eUeyama
doaj +1 more source
How Does Hollywood Depict People With Disabilities in Films? [PDF]
, 2012 https://digitalcommons.usu.edu/cpd_blog/1610/thumbnail ...
Center for Persons With Disabilities
core +1 more source
Accessibility of Persons with Disabilities on the Review of Disability Fiqh
Santri: Journal of Pesantren and Fiqh Sosial, 2020 Accessibility is a form of sympathy and empathy to provide convenience to persons with disabilities by providing friendly public facilities. This study aims to explain how the physical facilities provided by the Pesantren Institute Mathali'ul Falah (IPMAFA) Pati in accommodating people with disabilities in learning and the application of religious fiqh
Puji Lestari, Raodah Raodah
openaire +3 more sources