Results 11 to 20 of about 34,485 (311)

Review—Emerging Portable Technologies for Gait Analysis in Neurological Disorders [PDF]

open access: yesFrontiers in Human Neuroscience, 2022
The understanding of locomotion in neurological disorders requires technologies for quantitative gait analysis. Numerous modalities are available today to objectively capture spatiotemporal gait and postural control features. Nevertheless, many obstacles prevent the application of these technologies to their full potential in neurological research and ...
Christina Salchow-Hömmen   +8 more
openaire   +5 more sources

Neurological gait disorders in childhood [PDF]

open access: yesPaediatrics and Child Health, 2018
Abstract There are an enormous number of neurological illnesses that can manifest with gait disturbance in childhood. Whilst experience and clinical acumen are helpful in diagnosing these disorders, some basic principles in assessment and diagnosis are helpful in determining the phenomenology, time course, and neuro-anatomical localisation.
Smith, Martin, Kurian, Manju
openaire   +2 more sources

Detection of Gait Abnormalities caused by Neurological Disorders [PDF]

open access: yes2020 IEEE 22nd International Workshop on Multimedia Signal Processing (MMSP), 2020
6 pages, 5 figures, Accepted by IEEE Workshop on Multimedia Signal Processing (MMSP ...
Goyal, Daksh   +2 more
openaire   +2 more sources

Fall-related functional impairments in patients with neurological gait disorder [PDF]

open access: yesScientific Reports, 2020
AbstractFalls are common in patients with neurological disorders and are a primary cause of injuries. Nonetheless, fall-associated gait characteristics are poorly understood in these patients. Objective, quantitative gait analysis is an important tool to identify the principal fall-related motor characteristics and to advance fall prevention in ...
Ehrhardt, Angela   +6 more
openaire   +2 more sources

Using Sensor Technology to Measure Gait Capacity and Gait Performance in Rehabilitation Inpatients with Neurological Disorders [PDF]

open access: yesSensors, 2022
The aim of this study was to objectively assess and compare gait capacity and gait performance in rehabilitation inpatients with stroke or incomplete spinal cord injury (iSCI) using inertial measurement units (IMUs). We investigated how gait capacity (what someone can do) is related to gait performance (what someone does).
Maartje M. S. Hendriks   +5 more
openaire   +3 more sources

Gait Variability to Phenotype Common Orthopedic Gait Impairments Using Wearable Sensors

open access: yesSensors, 2022
Mobility impairments are a common symptom of age-related degenerative diseases. Gait features can discriminate those with mobility disorders from healthy individuals, yet phenotyping specific pathologies remains challenging.
Junichi Kushioka   +6 more
doaj   +1 more source

Anti-glutamic Acid Decarboxylase Antibody-associated Cerebellar Ataxia: A Case Report

open access: yesTürk Nöroloji Dergisi, 2021
Anti-glutamic acid decarboxylase antibodies (anti-GAD-ab) are associated with various neurologic conditions. High titers of anti-GAD-abs are observed in stiff person syndrome and subacute cerebellar degeneration. Type 1 diabetes mellitus (T1DM) and other
Miray Atacan Yaşgüçlükal   +6 more
doaj   +1 more source

Ataxia in children: early recognition and clinical evaluation [PDF]

open access: yes, 2017
Background: Ataxia is a sign of different disorders involving any level of the nervous system and consisting of impaired coordination of movement and balance.
Falsaperla, Raffaele   +6 more
core   +1 more source

Independent domains of daily mobility in patients with neurological gait disorders [PDF]

open access: yesJournal of Neurology, 2020
AbstractThe aim of this study was to establish a comprehensive and yet parsimonious model of daily mobility activity in patients with neurological gait disorders. Patients (N = 240) with early-stage neurological (peripheral vestibular, cerebellar, hypokinetic, vascular or functional) gait disorders and healthy controls (N = 35) were clinically assessed
Max Wuehr   +5 more
openaire   +4 more sources

Inducible arginase 1 deficiency in mice leads to hyperargininemia and altered amino acid metabolism [PDF]

open access: yes, 2013
Arginase deficiency is a rare autosomal recessive disorder resulting from a loss of the liver arginase isoform, arginase 1 (ARG1), which is the final step in the urea cycle for detoxifying ammonia. ARG1 deficiency leads to hyperargininemia, characterized
Ballantyne, Laurel L.   +6 more
core   +6 more sources

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