Results 111 to 120 of about 99,061 (305)

Traces of Sub-Lexical Dyslexia in a Semisyllabic Orthography

open access: yesOnline Journal of Health & Allied Sciences, 2017
Dyslexia refers to the impairment of reading ability. Different forms of dyslexia have been reported in the literature. A classic type of dyslexia in which children exhibit poor reading of non-words compared to true words is known as phonological ...
Suresh Kiran   +2 more
doaj  

How mobile app developers conceive of dyslexia and what it means for mobile app users

open access: yesInteraction Design and Architecture(s), 2016
This study surveys the landscape of 531 apps identified in a search for mobile apps for dyslexia and examines how their developers conceive of dyslexia.
Kara Dawson   +3 more
doaj   +1 more source

Dyslexia

open access: yes, 2009
Biblioteca de Educación del Ministerio de Educación, Cultura y Deporte; Calle San Agustín, 5 - 3 planta; 28014 Madrid; Tel.
openaire   +2 more sources

Speed and accuracy of dyslexic versus typical word recognition: an eye-movement investigation [PDF]

open access: yes, 2014
Developmental dyslexia is often characterized by a dual deficit in both word recognition accuracy and general processing speed. While previous research into dyslexic word recognition may have suffered from speed-accuracy trade-off, the present study ...
Kunert, Richard, Scheepers, Christoph
core   +2 more sources

No evidence that same‐language subtitles improve children's reading fluency

open access: yesBritish Journal of Psychology, EarlyView.
Abstract High‐profile campaigns globally have argued that same‐language television subtitles may help children improve their reading. In this intervention study, we tested the causal hypothesis that exposure to subtitles improves children's reading fluency.
Anastasiya Lopukhina   +4 more
wiley   +1 more source

Temporal sampling in vision and the implications for dyslexia

open access: yesFrontiers in Human Neuroscience, 2014
It has recently been suggested that dyslexia may manifest as a deficit in the neural synchrony underlying language-based codes (Goswami, 2011), such that the phonological deficits apparent in dyslexia occur as a consequence of poor synchronisation of ...
Kristen ePammer
doaj   +1 more source

A SWOT Analysis of Three Programmes for Persons With Intellectual Disabilities in Higher Education Settings in Chile, Ireland and Australia

open access: yesBritish Journal of Learning Disabilities, EarlyView.
ABSTRACT Background Educational access is key in empowering persons living with intellectual disabilities. Nevertheless, internationally, Persons with Intellectual Disabilities continue to experience marginalization and discrimination in accessing higher education.
Denise De Souza   +8 more
wiley   +1 more source

Higher education provision for students with disabilities in Cyprus [PDF]

open access: yes, 2007
Internationally, the number of students with disabilities entering higher education institutions is on the rise. Research estimates that 8–10% of students attending higher education are registered with disability, with learning difficulties being the ...
Hadjikakou, Kika, Hartas, Dimitra
core   +1 more source

The Recruitment and Retention of Individuals With Intellectual Disability in Randomized Controlled Trials: A Scoping Review

open access: yesBritish Journal of Learning Disabilities, EarlyView.
ABSTRACT Background People with intellectual disabilities face significant health disparities and often encounter barriers in accessing healthcare services. Although research supports the need for reasonable adjustments to improve healthcare access for this population, implementation in acute healthcare settings remains limited.
Owen Doody   +5 more
wiley   +1 more source

Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1

open access: yesGenetics and Molecular Biology, 2018
An increasing number of genetic variants involved in dyslexia development were discovered during the last years, yet little is known about the molecular functional mechanisms of these SNPs.
Bent Müller   +5 more
doaj   +1 more source

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