Results 101 to 110 of about 92,257 (361)

Compound heterozygosity of a De novo 16q24.1 deletion and missense mutation in COX4I1 leads to developmental regression, intellectual disability, and seizures

open access: yesEpilepsia Open, EarlyView.
Abstract The COX4I1 is responsible for encoding a crucial component of cytochrome c oxidase, integral to electron transport in the mitochondrial respiratory chain. Mutations in COX4I1 can result in a rare autosomal recessive disorder characterized by growth retardation, slow weight gain, microcephaly, and potentially, hematologic symptoms such as ...
Zhen Liu   +5 more
wiley   +1 more source

EEG Microstates Indicate Heightened Somatic Awareness in Insomnia: Toward Objective Assessment of Subjective Mental Content

open access: yesFrontiers in Psychiatry, 2018
People with Insomnia Disorder (ID) not only experience abundant nocturnal mentation, but also report altered spontaneous mental content during daytime wakefulness, such as an increase in bodily experiences (heightened somatic awareness). Previous studies
Yishul Wei   +8 more
doaj   +1 more source

Timing is everything: The effect of early‐life seizures on developing neuronal circuits subserving spatial memory

open access: yesEpilepsia Open, EarlyView.
Abstract Spatial memory, the aspect of memory involving encoding and retrieval of information regarding one's environment and spatial orientation, is a complex biological function incorporating multiple neuronal networks. Hippocampus‐dependent spatial memory is not innate and emerges during development in both humans and rodents.
Gregory L. Holmes
wiley   +1 more source

On the helical behavior of turbulence in the ship wake [PDF]

open access: yesarXiv, 2010
Turbulent ship wake conservation at a long distance is one of unsolved problems at present. It is well known that wakes have a rotational structure and slowly expand with distance. Nevertheless, experimental data on their structure and properties are not sufficient.
arxiv  

Oscillatory EEG activity during REM sleep in elderly people predicts subsequent dream recall after awakenings [PDF]

open access: yes, 2019
Several findings underlined that the electrophysiological (EEG) background of the last segment of sleep before awakenings may predict the presence/absence of dream recall (DR) in young subjects.
Bartolacci, Chiara   +5 more
core   +1 more source

Epilepsy syndromes classification

open access: yesEpilepsia Open, EarlyView.
Abstract Epilepsy syndromes are distinct electroclinical entities which have been recently defined by the International League Against Epilepsy Nosology and Definitions Task Force. Each syndrome is associated with “a characteristic cluster of clinical and EEG features, often supported by specific etiologic findings”.
Elaine C. Wirrell   +4 more
wiley   +1 more source

Etiology and Neuropathophysiology of Coma

open access: yesTürk Nöroloji Dergisi, 2012
Awareness and wakefulness require an intact connection of the neocortex with the ascending reticular formation. Any factor disrupting these pathways is likely to cause a syndrome of unconciousness. Disorders of consciousness encompass a broad spectrum of
Aslı Kıyat Atamer, Yakup Krespi
doaj   +1 more source

Stratified wake of an accelerating hydrofoil [PDF]

open access: yes, 2015
Wakes of towed and self-propelled bodies in stratified fluids are significantly different from non-stratified wakes. Long time effects of stratification on the development of the wakes of bluff bodies moving at constant speed are well known. In this experimental study we demonstrate how buoyancy affects the initial growth of vortices developing in the ...
arxiv   +1 more source

The inner portrait: What does reflexivity in qualitative health professions education research look like?

open access: yes
Anatomical Sciences Education, EarlyView.
Gabrielle Brand   +2 more
wiley   +1 more source

Decreased homovanillic acid and 5‐hydroxyindoleacetic acid levels in the cerebrospinal fluid of patients with Dravet syndrome with parkinsonism

open access: yesEpilepsia Open, EarlyView.
Abstract Dravet syndrome (DS) is an early onset, developmental, and epileptic encephalopathy characterized by drug‐resistant seizures and multiple comorbidities. It has been reported that in adulthood, it may be accompanied by parkinsonism, but the pathogenesis of this condition remains unclear.
Ryo Sugiyama   +5 more
wiley   +1 more source

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