Results 61 to 70 of about 781,361 (246)

Deep Learning Pose Estimation for Phenotyping of Co‐Occurring Hyperkinetic Movement Disorders

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To explore whether routine outpatient video combined with deep learning‐based pose estimation and clinically interpretable kinematic features can support multi‐label phenotyping of co‐occurring hyperkinetic movement disorders (HMDs).
Laura Cif   +17 more
wiley   +1 more source

The therapeutic usage of botulinum toxin (Botox) in non-cosmetic head and neck conditions – An evidence based review

open access: yesSaudi Pharmaceutical Journal, 2017
Botulinum toxin (Botox) is an exotoxin produced from Clostridium botulinum. It blocks the release of acetylcholine from the cholinergic nerve end plates resulting in inactivity of the muscles or glands innervated.
Kamran Habib Awan
doaj   +1 more source

Neurological, Neurodevelopmental and Treatment Outcomes in Patients With Pyruvate Dehydrogenase Complex Deficiency

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective The aim of this study was to characterize intellectual and motor function, neurological features including epilepsy, treatment response, and adaptive behavior in patients with pyruvate dehydrogenase complex deficiency (PDCD) in Sweden.
Antri Savvidou   +6 more
wiley   +1 more source

Neurophysiological Measures of Efficacy and Safety for Botulinum Toxin Injection in Facial and Bulbar Muscles: Special Considerations

open access: yesToxins, 2017
Botulinum toxin (BoNT) injections into facial and bulbar muscles are widely and increasingly used as medical treatments for cervical and facial dystonia, facial hemispasm, correction of facial palsy, hyperhidrosis, as well as cosmetic treatment of ...
Mohammad Alimohammadi   +1 more
doaj   +1 more source

Exteroceptive suppression in facial hyperkineses and dystonias

open access: yesNeurology Bulletin, 1997
On the basis of study of results of exteroceptive suppression parameters in 140 patients with different variants of facial hyperkineses the state of reflex inhibitory neuronal chains was defined more precisely. Received data may be used in process selection and monitoring of therapy and promote to understanding of facial musculature dyskinesia forming ...
Y. B. Judelson, N. Р. Gribova
openaire   +2 more sources

Utility of the APE2 Score as a Diagnostic Tool for Autoimmune Encephalitis

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To retrospectively evaluate the diagnostic performance of the Antibody Prevalence in Epilepsy and Encephalopathy (APE2) score relative to clinician‐adjudicated autoimmune encephalitis (AE) and the Graus criteria in a tertiary neuroimmunology referral cohort, including antibody‐negative AE.
Bijoya Basu   +3 more
wiley   +1 more source

Dopa-responsive dystonia and hyperprolactinaemia : a novel association in two sisters [PDF]

open access: yes, 2007
Dopa-Responsive Dystonia (DRD) is a rare hereditary condition of childhood-onset dystonia which responds dramatically to treatment with levodopa. It was first described in 1971 as a "hereditary progressive basal ganglia disease with marked diurnal ...
Cachia, Mario J., Galea, Janabel
core  

Accounting for Dystonia: Personalising Illness Through Narrative [PDF]

open access: yes, 2004
This paper explores how people living with dystonia, a chronic neurological condition involving involuntary muscle spasms in multiple body parts, use narrative to make sense of illness by linking past, present and future, and giving their condition ...
Camfield, Laura
core   +4 more sources

Recent findings in cranial and cervical dystonia: how they help us to understand the pathophysiology of dystonia.

open access: yes, 2006
Focal dystonia is a hyperkinetic movement disorder confined to a single body district. The most common forms are cranial and cervical dystonia.
S. Bagnato   +5 more
core   +1 more source

Treatment of Dystonia Using Trihexyphenidyl in Costello Syndrome

open access: yesBrain Sciences, 2020
Costello syndrome (CS), a rare syndrome with multisystemic involvement inherited as a dominant trait, is characterized by developmental delay, coarse facial appearance, cardiac defects including hypertrophic cardiomyopathy, skin abnormalities, brain ...
Domenico M. Romeo   +7 more
doaj   +1 more source

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