Results 1 to 10 of about 280,010 (207)
Smoothness of movement in idiopathic cervical dystonia [PDF]
Smoothness (i.e. non-intermittency) of movement is a clinically important property of the voluntary movement with accuracy and proper speed. Resting head position and head voluntary movements are impaired in cervical dystonia.
Antonio Caronni +10 more
doaj +2 more sources
Background: Cervical dystonia is a highly disabling hyperkinetic movement disorder with a lot of nonmotor symptoms. One symptom with a high prevalence is depression, which may negatively affect dystonia patients.
Vlada Meļņikova +3 more
doaj +1 more source
Multimodal Quantitative MRI Reveals No Evidence for Tissue Pathology in Idiopathic Cervical Dystonia
Background: While in symptomatic forms of dystonia cerebral pathology is by definition present, it is unclear so far whether disease is associated with microstructural cerebral changes in idiopathic dystonia.
René-Maxime Gracien +14 more
doaj +1 more source
Cervical dystonia: a disorder of the midbrain network for covert attentional orienting.
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
Evaluation of outcome of different neurosurgical modalities in management of cervical dystonia
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
CHEMODNERVATION FOR CERVICAL DYSTONIA: A CLINICAL REVIEW
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
Progressive Parkinsonism in PPP2R5D‐Related Neurodevelopmental Disorder
ABSTRACT PPP2R5D‐related neurodevelopmental disorder (Houge–Janssens syndrome type 1) is a rare autosomal dominant condition characterized by macrocephaly, intellectual disability, and epilepsy. Progressive parkinsonism is an emerging adult phenotype that neurologists should be aware of since timely genetic diagnosis opens the door to disease‐modifying
Katerina Bernardi +6 more
wiley +1 more source
Gait Alterations Due to DCC Gene Variants in Individuals with Congenital Mirror Movements
Abstract Background Congenital Mirror Movement Syndrome (CMMS) involves involuntary movements on one side of the body while voluntary movements are performed on the other side. They disrupt left–right coordination and can be caused by a pathogenic variant in the DCC gene.
Nok‐Yeung Law +7 more
wiley +1 more source
INTERFAMILIAL POLYMORPHISM OF TYPE 1 DYSTONIA
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
Abnormalities in the somatosensory system are increasingly being recognized in patients with dystonia. The aim of this study was to investigate whether sensory abnormalities are confined to the dystonic body segments or whether there is a wider ...
Lejla Paracka +10 more
doaj +1 more source

