F Lin, Y Li, J Wang, S Jardines, R King, MA Chrenek… - Scientific Reports, 2024 - nature.com
Pou6f2 is a genetic connection between central corneal thickness (CCT) in the mouse and a risk factor for developing primary open-angle glaucoma. POU6F2 is also a risk factor for …
In recent decades, theories have been presented to explain the nature of dyslexia, but the causes of dyslexia remained unclear. Although the investigation of the causes of dyslexia …
The present study aimed to investigate the improvement of reading ability and cognitive performance of children with reading difficulties through a Web application named “Poke the …
TR Fricke, AB Metha, DP Anderson… - Ophthalmic and …, 2023 - Wiley Online Library
Purpose To determine whether a typical vision therapy (VT) programme designed to improve visual information processing (VIP) skills is effective in improving these skills and/or …
A Premeti, F Isel, MP Bucci - Neurology International, 2024 - mdpi.com
Whether dyslexia is caused by phonological or attentional dysfunction remains a widely debated issue. To enrich this debate, we compared the eye movements of 32 French …
J Pérez-Rey, P Fanlo-Mazas, M Gil-Calvo - Advances in …, 2023 - Springer
Objectives Dyslexia is a learning disability with a prevalence of between 5 and 10% in Spain. There is a relationship between the cognitive and motor aspects, which is manifested …
ZMM Zaki, SA Ali, MM Ghazali… - Global Medical …, 2024 - thieme-connect.com
Dyslexia is a genetic and heritable disorder that has yet to discover the treatment of it, especially at the molecular and drug intervention levels. This review provides an overview of …
About 10% of the world's population is dyslexic, experiencing reading impairments unrelated to cognitive deterioration. Due to its impact, identifying the mechanisms …
Much progress has been made in research on the causal mechanisms of developmental dyslexia. In recent years, the 'temporal sampling'account of dyslexia has evolved …