Results 41 to 50 of about 15,494 (222)

Evaluation of outcome of different neurosurgical modalities in management of cervical dystonia

open access: yesThe Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2022
Background Cervical dystonia is the most common form of focal dystonia and is managed by multiple modalities including repeated botulinum toxin injections, in addition to medical treatment with anticholinergics, muscle relaxants, and physiotherapy ...
Mazen Alkarras   +6 more
doaj   +1 more source

Early Globus Pallidus Internus Stimulation in Pediatric Patients With Generalized Primary Dystonia: Long-Term Efficacy and Safety [PDF]

open access: yes, 2010
Primary generalized dystonia presents mainly at a young age and commonly is severely disabling. The authors report the long-term follow-up (mean, 73 months; range, 50-101 months) of 5 pediatric patients (mean age at surgery 13 years; range, 8-16 years ...
Berend Feddersen   +6 more
core   +1 more source

Isolated Cervical Dystonia: Diagnosis and Classification

open access: yesMovement Disorders, 2023
AbstractThis document presents a consensus on the diagnosis and classification of isolated cervical dystonia (iCD) with a review of proposed terminology. The International Parkinson and Movement Disorder Society Dystonia Study Group convened a panel of experts to review the main clinical and diagnostic issues related to iCD and to arrive at a consensus
Alberto Albanese   +14 more
openaire   +6 more sources

Increased prevalence of val(66)met BDNF genotype among subjects with cervical dystonia [PDF]

open access: yes, 2010
Abnormalities of cortical representational maps and their plasticity have been described in dystonia. A common polymorphism for BDNF has been associated with abnormal cortical plasticity, and thus might contribute to pathogenesis of dystonia in some ...
A. Sampat   +5 more
core   +5 more sources

Cervical dystonia: a disorder of the midbrain network for covert attentional orienting.

open access: yesFrontiers in Neurology, 2014
While the pathogenesis of cervical dystonia remains unknown, recent animal and clinical experimental studies have indicated its probable mechanisms. Abnormal temporal discrimination is a mediational endophenotype of cervical dystonia and informs new ...
Michael eHutchinson   +18 more
doaj   +1 more source

CHEMODNERVATION FOR CERVICAL DYSTONIA: A CLINICAL REVIEW

open access: yesKhyber Medical University Journal, 2020
Cervical dystonia (CD) is a focal dystonia characterized by involuntary contractions of neck muscles that result in patterned movements and abnormal postures of the head and neck that have a directional quality.
Muhammad Atif Ameer, Danish Bhatti
doaj   +1 more source

Epoetin alfa increases frataxin production in Friedreich's ataxia without affecting hematocrit. [PDF]

open access: yes, 2011
Objective of the study was to test the efficacy, safety, and tolerability of two single doses of Epoetin alfa in patients with Friedreich's ataxia. Ten patients were treated subcutaneously with 600 IU/kg for the first dose, and 3 months later with 1200 ...
ACQUAVIVA, Fabio   +13 more
core   +1 more source

Structural and Functional Imaging of Motor Outcomes in Twins With Perinatal Stroke: A Case Report

open access: yesAnnals of the Child Neurology Society, EarlyView.
ABSTRACT Background Perinatal arterial ischemic stroke (AIS) affects 1 in 4000 live births. Dystonia, affecting ~20% of children following AIS, is characterized by involuntary muscle contractions and abnormal movements. Why some develop dystonia post AIS, while others do not, remains unclear.
Prisca Hsu   +8 more
wiley   +1 more source

Botulinum toxin type B for cervical dystonia [PDF]

open access: yes, 2016
BACKGROUND: This is an update of a Cochrane review first published in 2004, and previously updated in 2009 (no change in conclusions). Cervical dystonia is a frequent and disabling disorder characterised by painful involuntary head posturing.
Castelão, M   +7 more
core   +1 more source

INTERFAMILIAL POLYMORPHISM OF TYPE 1 DYSTONIA

open access: yesAlʹmanah Kliničeskoj Mediciny, 2016
Background: The most frequent mutation of the gene TOR1A (DYT1) (9q34), that causes type 1 dystonia (DOPA-unresponsive torsion dystonia) is the deletion c.907-909delGAG in the 5th exon of the gene (303delGlu).
K. A. Ostapchuk   +5 more
doaj   +1 more source

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