Results 21 to 30 of about 11,724 (249)

Diagnosis and treatment of functional dystonia

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2023
Functional dystonia is one of the most common phenotypes of functional movement disorder (FMD). Multiple clinical manifestations of functional dystonia are complex and some symptoms overlap with idiopathic dystonia.
LI Shu‑hua, SU Wen, CHEN Hai‑bo
doaj   +1 more source

Faciobrachial dystonic seizure-like events in a patient with subacute sclerosing panencephalitis

open access: yesAnnals of Movement Disorders, 2022
Faciobrachial dystonic seizure is a distinctive phenomenology that is considered pathognomonic of leucine-rich glioma-inactivated protein 1 (LGI1) antibody-associated autoimmune limbic encephalitis.
Vikram V Holla   +5 more
doaj   +1 more source

The Signature of Primary Writing Tremor Is Dystonic [PDF]

open access: yes, 2021
Background: It has been debated for decades whether primary writing tremor is a form of dystonic tremor, a variant of essential tremor, or a separate entity.
Rocchi L.   +5 more
core   +1 more source

The Central Effects of Botulinum Toxin in Dystonia and Spasticity

open access: yesToxins, 2021
In dystonic and spastic movement disorders, however different in their pathophysiological mechanisms, a similar impairment of sensorimotor control with special emphasis on afferentation is assumed.
Pavel Hok   +4 more
doaj   +1 more source

Spotlight on Oculogyric Crisis: A Review

open access: yesIndian Journal of Psychological Medicine, 2021
Background: Oculogyric crisis (OGC) is a form of acute dystonia characterized by sustained dystonic, conjugate, and upward deviation of the eyes. It was initially reported in patients with postencephalitic parkinsonism.
Pankaj Mahal   +2 more
doaj   +1 more source

A childhood ⁃ onset rapid ⁃ onset dystonia Parkinsonism patient with ATP1A3 gene mutation and literature review

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2021
Objective To study the clinical characteristics, diagnosis, treatment and prognosis of a patient with childhood⁃onset rapid⁃onset dystonia Parkinsonism (RDP) caused by ATP1A3 gene mutation, and review the related literature.
KANG Qing⁃yun   +4 more
doaj   +1 more source

Dystonic tremor and blepharospasm in a patient with deletion of 18q [PDF]

open access: yes, 2023
18q- Syndrome is a rare chromosomic syndrome where neurological involvement is scarcely described. Movement disorders are rare and only one case with dystonia was described.
Valente M.   +6 more
core   +1 more source

Impaired eye blink classical conditioning distinguishes dystonic patients with and without tremor [PDF]

open access: yes, 2016
INTRODUCTION: Tremor is frequently associated with dystonia, but its pathophysiology is still unclear. Dysfunctions of cerebellar circuits are known to play a role in the pathophysiology of action-induced tremors, and cerebellar impairment has frequently
Rothwell, J.   +27 more
core   +3 more sources

Recognising the common origins of dystonia and the development of human movement: A manifesto of unmet needs in isolated childhood dystonias

open access: yesFrontiers in Neurology, 2016
Dystonia in childhood may be severely disabling and often un-remitting and un-recognised. Considered a rare disorder, dystonic symptoms in childhood are pervasive in many conditions including disorders of developmental delay, cerebral palsy, autism ...
Jean-Pierre Lin, Nardo Nardocci
doaj   +1 more source

Metoclopramide-Induced Acute Dystonic Reaction: A Case Report

open access: yesEurasian Journal of Medicine, 2019
The aim of this case report is to draw attention to the frequent occurrence of metoclopramide-induced movement disorders. We report a case of an acute dystonic reaction to metoclopramide in a patient treated for hepatitis A.
Gul Karagoz   +5 more
doaj   +1 more source

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