Results 141 to 150 of about 2,981,639 (311)
ABSTRACT Objective We aim to comprehensively analyze how regional tumor and edema characteristics are associated with clinical presentations and survival outcomes in a large cohort of glioblastoma patients. Methods Patients with IDH‐wildtype glioblastoma who received brain MRI from 2010 to 2023 were included.
Daniel J. Zhou +16 more
wiley +1 more source
Autism Spectrum Disorders and Visual Impairment Meeting Students' Learning Needs
Intro -- Title Page -- Copyright Page -- Table of Contents -- Foreword -- Preface -- Part 1 Understanding Autism Spectrum Disorders and Visual Impairment -- Prologue Learning, Teaching, Learning -- Chapter 1 Autism Spectrum Disorders: An Introduction ...
Gense, Marilyn H., Gense, D. Jay.
core
Accessibility of cities involves designing spaces and services to enable everyone to live independently and fully participate in urban life. This study aims to gather the perspectives of individuals with visual impairment on the accessibility of everyday
Barbara Arfè +23 more
core +1 more source
MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children
ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru +13 more
wiley +1 more source
Summary: • Cortical Visual Impairment o Term preferred over cortical blindness as patient does not need to be blind o Impaired with vision due to problem in the occipital cortex o Any lesion behind the optic chiasm bodies > homonymous hemianopsia on the ...
Andrew G. Lee, MD; Jae Eun Lee
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ABSTRACT Objective To characterize the demographic, clinical, and laboratory features of the Chinese patients of genetic Creutzfeldt‐Jakob disease with T188K variant (T188K‐gCJD), the most common subtype of genetic prion diseases (gPrDs) in China. Methods In this nationwide retrospective study, data from 98 genetically confirmed T188K‐gCJD patients ...
Chun‐Jie Li +11 more
wiley +1 more source
ABSTRACT Objective Variants in SLC6A1, encoding the GABA transporter 1 (GAT‐1), cause epilepsy, autism spectrum disorder, and developmental delay via loss of GABA uptake, impaired trafficking, and ER retention. We previously found that 4‐Phenylbutyrate (PBA), an FDA‐approved drug, restores GABA uptake and reduces seizures in SLC6A1‐related disorders ...
Melissa B. DeLeeuw +5 more
wiley +1 more source
Being siblings of children with visual impairment
This is a qualitative study that gives voice to 33 siblings of children with visual impairment in care at the Robert Hollman Foundation, focusing on their relationships with their brothers/sisters. Participants aged 7 to 22 recounted their daily life
Tiziana Battistin +4 more
core +1 more source
ABSTRACT Objectives We aimed to determine the frequency of subclinical optic nerve (ON) lesions using MRI, optical coherence tomography (OCT), and visual evoked potentials (VEP) in radiologically isolated syndrome (RIS), and to assess their diagnostic and prognostic significance.
Christine Lebrun‐Frenay +13 more
wiley +1 more source
ABSTRACT Objective Neurochemical levels measured by brain MR spectroscopy (MRS) have been proposed as endpoints for clinical trials in early‐stage spinocerebellar ataxia (SCA) trials. We tested their trial‐readiness by quantifying neurochemicals in three affected brain regions in early‐stage cohorts of SCA2 and SCA3, examining their reproducibility in ...
James M. Joers +19 more
wiley +1 more source

