Results 51 to 60 of about 6,026,001 (259)

Posterior Cortical Atrophy in the Asia‐Pacific: A Report From the PCA Asian Workgroup

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Posterior Cortical Atrophy (PCA) is a distinct dementia syndrome primarily affecting spatial abilities and visual processing. It is associated with degeneration in the posterior part of the brain. PCA is subclassified into PCA‐pure and PCA‐plus syndromes based on consensus criteria.
Yuttachai Likitjaroen   +11 more
wiley   +1 more source

Smartwatch-monitored physical activity and myopia in children: a 2-year prospective cohort study

open access: yesBMC Medicine
Background While outdoor time's protective role against myopia is established, the relationship between physical activity (PA) and myopia development remains unclear. This study aimed to determine the impact of PA on myopia in children.
Daixi Chen   +12 more
doaj   +1 more source

The associations of lens power with age, axial length and type 2 diabetes mellitus in Chinese adults aged 50 and above

open access: yesEye and Vision, 2020
Background To investigate the associations of lens power with age, axial length (AL), and Type 2 diabetes mellitus (DM) in Chinese adults aged 50 and above.
Luyao Ye   +10 more
doaj   +1 more source

Elevated Connectivity During Language Processing Is Associated With Cognitive Performance in SeLECTS

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Self‐Limited Epilepsy with Centrotemporal Spikes (SeLECTS) is associated with language impairments despite seizures originating in the motor cortex, suggesting aberrant cross‐network interactions. Here we tested whether functional connectivity in SeLECTS during language tasks predicts language performance.
Wendy Qi   +8 more
wiley   +1 more source

Evaluating imaging repeatability of fully self-service fundus photography within a community-based eye disease screening setting

open access: yesBioMedical Engineering OnLine
Purpose This study aimed to investigate the imaging repeatability of self-service fundus photography compared to traditional fundus photography performed by experienced operators. Design Prospective cross-sectional study. Methods In a community-based eye
Juzhao Zhang   +13 more
doaj   +1 more source

Finger-Prick Autologous Blood (FAB) Eye Drops for Dry Eye Disease: Single Masked Multi-Centre Randomised Controlled Trial

open access: yes, 2022
Ali Hassan,1,2,* Shafi Balal,1,2,* Erica Cook,3 Hakim-Moulay Dehbi,4 Shahina Pardhan,5 Rupert Bourne,6 Sajjad Ahmad,1,2 Anant Sharma1,2 1Department of External Eye Diseases, Moorfields Eye Hospital, London, UK; 2Department of Ophthalmology, UCL ...
Bourne R   +7 more
core  

SPG4 and Dementia: Expanding the Clinical Spectrum

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza   +19 more
wiley   +1 more source

Classification of pathology in diabetic eye disease [PDF]

open access: yes, 2005
Proliferative diabetic retinopathy is a complication of diabetes that can eventually lead to blindness. Early identification of this complication reduces the risk of blindness by initiating timely treatment.
Cesar, R.M., Jr.   +3 more
core   +1 more source

EyeTFDB: a Curated Eye Disease Transcription Factor Web-Based Platform [PDF]

open access: yes, 2020
Background:  The TFs identify as distinct DNA sequences to regulate transcription processes and chromatin forming.   Materials and Methods: To address needs in multiple areas, we present the EyeTFDB (https://eyetfdb.databanks.behrc.ir/) web ...
Pournoor, Ehsan   +2 more
core   +1 more source

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu   +21 more
wiley   +1 more source

Home - About - Disclaimer - Privacy