Results 21 to 30 of about 10,678 (188)

Cannabidiol as a Promising Strategy to Treat and Prevent Movement Disorders?

open access: yesFrontiers in Pharmacology, 2018
Movement disorders such as Parkinson's disease and dyskinesia are highly debilitating conditions linked to oxidative stress and neurodegeneration. When available, the pharmacological therapies for these disorders are still mainly symptomatic, do not ...
Fernanda F. Peres   +9 more
doaj   +1 more source

Neurodegeneration with Brain Iron Accumulation: Two Additional Cases with Dystonic Opisthotonus

open access: yesTremor and Other Hyperkinetic Movements, 2019
Background: Specific phenomenology and pattern of involvement in movement disorders point toward a probable clinical diagnosis. For example, forehead chorea usually suggests Huntington’s disease; feeding dystonia suggests neuroacanthocytosis and risus ...
Sahil Mehta, Vivek Lal
doaj   +1 more source

Limbic encephalitis associated with leucine-rich glioma-inactivated 1 antibodies

open access: yesAnnals of Saudi Medicine, 2015
We describe the case of a patient with confirmed limbic encephalitis associated with leucine-rich glioma-inactivated 1 (LGI1) antibodies. A 59-year-old man presented to the Department of Neurology with bizarre behavior, memory loss, cognitive impairment,
Mariem Messelmani   +3 more
doaj   +1 more source

Metoclopramide-induced acute dystonic reaction misinterpreted as conversion disorder and seizure [PDF]

open access: yesElectronic Journal of General Medicine, 2017
Metoclopramide, an antiemetic, is the most common cause of drug-induced dystonic reactions. 20-year-old female patient, complaining of involuntary bilateral upward medial deviation of the eyes, generalized muscle contractions and uncontrollable cry was brought into the emergency department(ED) by an ambulance.
Betul Akbuga-Ozel   +6 more
openaire   +1 more source

FOCAL DYSTONIAS: NON-MOTOR SYMPTOMS AND COMORBIDITIES

open access: yesМедицинский совет, 2017
Dystonia is a common extrapyramidal disease. It is characterized by both motor and non-motor manifestations, which include pain, sensory disorders and excessive physical activity.
V. A. Tolmachyova
doaj   +1 more source

Torsin ATPases: Harnessing Dynamic Instability for Function

open access: yesFrontiers in Molecular Biosciences, 2017
Torsins are essential, disease-relevant AAA+ (ATPases associated with various cellular activities) proteins residing in the endoplasmic reticulum and perinuclear space, where they are implicated in a variety of cellular functions.
Anna R. Chase   +3 more
doaj   +1 more source

Wearable Metamaterials with Embodied Intelligence for Programmable Control of Human Limbs Tremor

open access: yesAdvanced Intelligent Systems, EarlyView.
Resulting from alternating muscle contractions, tremors can severely limit human ability to perform everyday tasks like walking or talking, due to their disruptive nature. Medication and surgery may not always effectively address tremor control. A wearable device embodying programmable smart metamaterials with adaptable intelligence to meet the demand ...
Braion Barbosa de Moura   +2 more
wiley   +1 more source

Comparison of clinical characteristics of patients with adductor laryngeal dystonia in the focal and segmental types Comparação entre características clínicas de pacientes com distonia laríngea de adução nas formas focal e segmentar

open access: yesBrazilian Journal of Otorhinolaryngology, 2011
Dystonia is a central motor processing neurological disorder characterized by abnormal, often action-induced, involuntary movements or uncontrolled spasms.
Gustavo Polacow Korn   +6 more
doaj   +1 more source

RHOBTB2 gene associated epilepsy and paroxysmal movement disorder: two cases report and literature review

open access: yesActa Epileptologica, 2021
Background RHOBTB2 gene is associated with developmental and epileptic encephalopathy-64(DEE-64), which is characterized by epilepsy, developmental delay, microcephaly, unspecific facial dysmorphism, and paroxysmal movement disorders.
Xueyang Niu   +6 more
doaj   +1 more source

Cytosolic Phosphoenoylpyruvate Carboxykinase Deficiency: Clinical, Biochemical, and Genetic Features of Five Non‐Finnish Patients

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cytosolic phosphoenoylpyruvate carboxykinase (PEPCK‐C) is an essential, rate‐limiting enzyme in the gluconeogenesis pathway. PEPCK‐C deficiency presents with hypoglycaemia, hyperlactataemia and hepatopathy, and was first reported in association with bi‐allelic PCK1 variants in 2014.
Isaac Bernhardt   +9 more
wiley   +1 more source

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