Results 181 to 190 of about 874,261 (376)

Brain Ischemia Instantaneously Tracked by the Narcotrend EEG Device [PDF]

, 2013
Harald Rinösl, Tatjana Fleck, Martin Dworschak   +2 more
openalex   +1 more source

A review of classification algorithms for EEG-based brain–computer interfaces: a 10 year update

Journal of Neural Engineering, 2018
F. Lotte, L. Bougrain, A. Cichocki, Maureen Clerc, M. Congedo, A. Rakotomamonjy, F. Yger   +6 more
semanticscholar   +1 more source

Analysis of Meditation vs. Sensory Engaged Brain States Using Shannon Entropy and Pearson’s First Skewness Coefficient Extracted from EEG Data [PDF]

, 2023
J. J. Joshua Davis, Róbert Kozma, Florian Schübeler   +2 more
openalex   +1 more source

Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat, Marjolaine Champagne, Mathieu Bergeron, Philippe Dodin, Nadia Roumeliotis   +4 more
wiley   +1 more source

Non-Invasive Intracranial Monitoring for Detection of Epilepsy Using EEG Signals [PDF]

Shreyas Sunil, Lakshmikanth reddy, Nandha Kumar S, Nsenga Ngoie, Pavan Krishna K R   +4 more
openalex   +1 more source

Decision letter for "Built to last: Theta and delta changes in resting‐state EEG activity after regulating emotions"

, 2021

openalex   +1 more source

Long‐Read Genome Sequencing Establishes Biallelic Pathogenic Variants in DNM1 With Distinct Functional Effects as the Cause of Early Infantile Developmental and Epileptic Encephalopathy

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous de novo and inherited biallelic pathogenic variants in DNM1 have been reported in association with autosomal dominant (AD) and autosomal recessive (AR) developmental and epileptic encephalopathy, respectively, due to aberrant dynamin function or expression, with each inheritance pattern associated with a different mechanism of ...
Andy Drackley, Merlene Peter, Heba H. Akbari, Jelena Ivanisevic, Alexander Ing, Kelly Regan‐Fendt, Patrick McMullen, Kai Lee Yap   +7 more
wiley   +1 more source

The First Reported Case of an Inherited Pathogenic Variant in DEAF1 From a Parent With Milder Phenotype Provides Evidence of Variable Gene Expressivity of the DEAF1‐Associated Vulto‐van Silfout‐de Vries Syndrome (VSVS)

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT DEAF1‐associated neurodevelopmental disorder (DAND) is a neurodevelopmental spectrum disorder caused by two methods of inheritance: the autosomal dominant intellectual disability syndrome (Vulto‐van Silfout‐de Vries syndrome (VSVS), OMIM #615828), and the autosomal recessive Neurodevelopmental disorder with hypotonia and impaired expressive ...
Kylie Katz, Philip Jensik, Milen Velinov
wiley   +1 more source

EEG: Electroencephalography

Journal of Criminal Law and Criminology (1931-1951), 1947
openaire   +3 more sources

Differential roles of EA‐TRAPed cells in the anterior cingulate cortex across various intervention times in inflammatory pain

Animal Models and Experimental Medicine, EarlyView.
The cumulative effect of EA analgesia is partially attributed to the activation of EA‐TRAPed cells in ACC. Multiple EA sessions and single EA sessions activated different neuronal populations in the ACC. The enhanced analgesic effect of multiple EA sessions may be attributed to an increase in the proportion of GABAergic neurons within the ACC. Abstract
Zi Guo, Ru Ye, Lu Guan, Wei He, Shuang Qiu, Xiaomei Shao, Junfan Fang, Jianqiao Fang, Junying Du   +8 more
wiley   +1 more source