Results 61 to 70 of about 269,933 (348)

Life‐Threatening Bradycardia in Anti‐NMDA‐Receptor Encephalitis and a Novel Use for Permanent Pacing

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Pediatric anti‐NMDA receptor encephalitis (pNMDARE) is an autoantibody‐mediated disorder that can cause severe autonomic dysfunction, including symptomatic bradycardia and asystole. Dysautonomia can last for years, making it very challenging to manage.
Sarah Tucker   +9 more
wiley   +1 more source

Effects of Sports Shoe Drop on Walking Biomechanics: A Cross-Sectional Observational Dynamometric Study

open access: yesApplied Sciences
Sports footwear is widely used across a range of physical activities. A key factor distinguishing running shoes from other types of footwear is the “drop,” the millimeter difference between the heel and the forefoot.
Raquel Fragua-Blanca   +4 more
doaj   +1 more source

Feasibility of Training a Random Forest Model With Incomplete User-Specific Data for Devising a Control Strategy for Active Biomimetic Ankle

open access: yesFrontiers in Bioengineering and Biotechnology, 2020
Intelligent control strategies for active biomimetic prostheses could exploit the inter-joint coordination of limbs in human gait in order to mimic the functioning of a biological joint.
Sharmita Dey   +2 more
doaj   +1 more source

The effect of time on gait recognition performance [PDF]

open access: yes, 2012
Many studies have shown that it is possible to recognize people by the way they walk. However, there are a number of covariate factors that affect recognition performance.
Carter, John   +3 more
core   +1 more source

Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Dystonia is one of the most common movement disorders, with variants in multiple genes identified as causative. However, an understanding of which developmental stages, brain regions, and cell types are most relevant is crucial for developing relevant disease models and therapeutics.
Darren Cameron   +5 more
wiley   +1 more source

Skeleton-Based Abnormal Gait Detection

open access: yesSensors, 2016
Human gait analysis plays an important role in musculoskeletal disorder diagnosis. Detecting anomalies in human walking, such as shuffling gait, stiff leg or unsteady gait, can be difficult if the prior knowledge of such a gait pattern is not available ...
Trong-Nguyen Nguyen   +2 more
doaj   +1 more source

A functional electrical stimulation system for human walking inspired by reflexive control principles [PDF]

open access: yes, 2017
This study presents an innovative multichannel functional electrical stimulation gait-assist system which employs a well-established purely reflexive control algorithm, previously tested in a series of bipedal walking robots.
Gollee, Henrik   +3 more
core   +1 more source

Super‐Refractory Status Epilepticus (SRSE) in a Patient With Compound Heterozygous OPA1 Variants: Case Report and Literature Review

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi   +2 more
wiley   +1 more source

Learning Human Gait

open access: yes, 2019
Pedestrian navigation in body-worn devices is usually based on global navigation satellite systems (GNSS), which is a sufficient solution in most outdoor applications. Pedestrian navigation indoors is much more challenging. Further, GNSS does not provide any specific information about the gait style or how the device is carried.
openaire   +4 more sources

Variably Protease‐Sensitive Prionopathy: Two New Cases With Motor Neuron‐Dementia Syndrome

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT We describe two patients with variably protease‐sensitive prionopathy (VPSPr) who developed progressive upper motor neuron symptoms, insomnia, behavioral and cognitive decline, compatible with primary lateral sclerosis associated with frontotemporal dementia (FTD).
María Elena Erro   +10 more
wiley   +1 more source

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