Results 51 to 60 of about 1,096,365 (243)

Outcome of Neonates with Agenesis of Septum Pellucidum: A Retrospective Single Center Study [PDF]

open access: yesNeonatal Medicine, 2019
Purpose Agenesis of the septum pellucidum (ASP) is a very rare disease that can be isolated or associated with other brain abnormalities. The neurological prognosis of isolated ASP remains controversial. The aim of this study was to evaluate the clinical
Yong Hee Kim   +3 more
doaj   +1 more source

Epileptiform activity in the acute phase of stroke predicts the outcomes in patients without seizures

open access: yesFrontiers in Neurology, 2023
Background and purposeThe abnormalities in EEG of stroke-patients increase the risk of epilepsy but their significancy for poststroke outcome is unclear. This presented study was aimed at determining the prevalence and nature of changes in EEG recordings
Anetta Lasek-Bal   +16 more
doaj   +1 more source

Circulating microRNA signatures of cachexia and cancer in Canis familiaris as a comparative oncology model for human disease

open access: yesMolecular Oncology, EarlyView.
Circulating microRNAs as biomarkers of cachexia and sex‐specific cancer in senior dogs. In 25 client‐owned dogs, four circulating miRNAs (miR‐15a, miR‐15b, miR‐16, miR‐140) were downregulated in cachexia, with miR‐16 the strongest individual biomarker (AUC = 0.899).
Soon‐Seok Park   +6 more
wiley   +1 more source

Early neurodevelopmental outcomes in children with asymptomatic congenital CMV infection

open access: yesItalian Journal of Pediatrics, 2022
Background Approximately 85–90% of congenital cytomegalovirus infections (cCMV) are asymptomatic. Few studies have investigated early and long-term neurodevelopmental outcomes in children with asymptomatic cCMV (acCMV), and the data is contradictory.
Maria Novelli   +7 more
doaj   +1 more source

Neurological abnormalities in young adults born preterm

open access: yes, 2006
Objective: Individuals born before 33 weeks' gestation (very preterm, VPT) have an increased likelihood of neurological abnormality, impaired cognitive function, and reduced academic performance in childhood.
Allin, M   +6 more
core   +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

Neuroscience Empowering Society: BCI Insights and Application

open access: yesEngineering Proceedings
The study of brainwaves and brain–computer interfaces (BCIs) or brain–machine interfaces (BMIs) has emerged as a transformative field with the potential to revolutionize society’s well-being.
Harish S. Sinai Velingkar   +2 more
doaj   +1 more source

Characteristics of neurological Wilson’s disease with corpus callosum abnormalities

open access: yesBMC Neurology, 2019
Background Wilson’s disease (WD) is an autosomal recessive disease of impaired copper metabolism. Previous study demonstrated that WD with corpus callosum abnormalities (WD-CCA) was limited to the posterior part (splenium).
Zhi-Hua Zhou   +8 more
doaj   +1 more source

Nitrous oxide‐related neurological disorders: Clinical, laboratory, neuroimaging, and electrophysiological findings

open access: yesBrain and Behavior, 2021
Background Recreational N2O abuse is an important etiology of neurological impairment in young patients, which may easily be ignored clinically. Few current studies have investigated the characteristics or the effects experienced by its users.
Jiwei Jiang   +6 more
doaj   +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

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