Results 51 to 60 of about 692,450 (357)

Liraglutide for idiopathic intracranial hypertension: a real‐world propensity score‐matched study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
Abstract Objective Idiopathic intracranial hypertension (IIH) is a neurological disorder predominantly affecting young women with obesity, characterized by elevated intracranial pressure. While current treatments include weight loss counseling, medical therapies, and surgical interventions, their limitations necessitate exploring novel therapeutic ...
Ahmed Y. Azzam   +13 more
wiley   +1 more source

Parental Awareness of the Preschool Orthoptics Visual Screening in Brunei-Muara District and Factors Contributing to Defaulters

open access: yesBritish and Irish Orthoptic Journal
Background: The preschool orthoptics visual screening program began in Brunei Darussalam in 2004 to detect amblyopia, a common cause of treatable visual disorders in children.
Sharimawati Sharbini   +3 more
doaj   +1 more source

A Survey on Deep Learning for Neuroimaging-based Brain Disorder Analysis [PDF]

open access: yesarXiv, 2020
Deep learning has been recently used for the analysis of neuroimages, such as structural magnetic resonance imaging (MRI), functional MRI, and positron emission tomography (PET), and has achieved significant performance improvements over traditional machine learning in computer-aided diagnosis of brain disorders.
arxiv  

Hierarchical Graph Convolutional Network Built by Multiscale Atlases for Brain Disorder Diagnosis Using Functional Connectivity [PDF]

open access: yesarXiv, 2022
Functional connectivity network (FCN) data from functional magnetic resonance imaging (fMRI) is increasingly used for the diagnoses of brain disorders. However, state-of-the-art studies used to build the FCN using a single brain parcellation atlas at a certain spatial scale, which largely neglected functional interactions across different spatial ...
arxiv  

Cerebello‐Prefrontal Connectivity Underlying Cognitive Dysfunction in Spinocerebellar Ataxia Type 2

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Spinocerebellar ataxia type 2 (SCA2) is a hereditary cerebellar degenerative disorder, with motor and cognitive symptoms. The constellation of cognitive symptoms due to cerebellar degeneration is named cerebellar cognitive affective syndrome (CCAS), which has increasingly been recognized to profoundly impact patients' quality of life;
Ami Kumar   +7 more
wiley   +1 more source

Oral health disorders among visually impaired children in South Asian countries: a systematic review

open access: yesFrontiers in Oral Health
Background and aimDespite the convergence of visual impairment and poor oral health among children, there is a scarcity of data on the common oral health disorders and their prevalence among children with visual impairments in South Asia.
Vini Mehta   +9 more
doaj   +1 more source

Postoperative visual disturbance: “A peril related to glycine toxicity”

open access: yesJournal of Marine Medical Society, 2018
Hysteroscopic gynecological surgeries are now commonly employed in the clinical practice. It has the potential to increase morbidity due to the complication resulting from perforation of the uterus, air/gas embolism, and fluid with electrolyte imbalance.
Deepak Dwivedi   +3 more
doaj   +1 more source

Computer visual syndrome in medical students in virtual education of a Peruvian university during 2021

open access: yesRevista de la Facultad de Medicina Humana, 2023
Introduction: Students during virtual classes due to COVID-19 may develop computer visual syndrome (SVI) due to excessive time in front of digital screens.
Rosario Mercedes Meneses Castañeda   +5 more
doaj   +1 more source

Computational Pathology for Brain Disorders [PDF]

open access: yesarXiv, 2023
Non-invasive brain imaging techniques allow understanding the behavior and macro changes in the brain to determine the progress of a disease. However, computational pathology provides a deeper understanding of brain disorders at cellular level, able to consolidate a diagnosis and make the bridge between the medical image and the omics analysis.
arxiv  

The Cone Dysfunction Syndromes [PDF]

open access: yes, 2016
The cone dysfunction syndromes are a heterogeneous group of inherited, predominantly stationary retinal disorders characterised by reduced central vision, and varying degrees of colour vision abnormalities, nystagmus and photophobia.
Aboshiha, J   +4 more
core  

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