Results 251 to 260 of about 52,972 (303)

No Evidence for an Association Between DIP2B Repeat Expansion and Neurological Disease

open access: yes
Movement Disorders, EarlyView.
Chia‐Ying Ko   +9 more
wiley   +1 more source

Dystonia

Continuum, 2013
The purpose of this review is to provide an update on the classification, phenomenology, pathophysiology, and treatment of dystonia.A revised definition based on the main phenomenologic features of dystonia has recently been developed in an expert consensus approach. Classification is based on two main axes: clinical features and etiology.
MORGANTE, FRANCESCA, Klein C.
openaire   +4 more sources

Dystonia

Clinics in Geriatric Medicine, 2006
Dystonia is a disorder of involuntary sustained muscle contractions. It is commonly classified by age of onset, distribution of involved body regions, and etiology. The pathophysiolgy of this condition is complex and imperfectly understood. This article reviews the epidemiology, genetics, clinical features, and approach to diagnosis and treatment of ...
Daniel, Tarsy, David K, Simon
openaire   +4 more sources

The Dystonias

Continuum, 2022
This article discusses the most recent findings regarding the diagnosis, classification, and management of genetic and idiopathic dystonia.A new approach to classifying dystonia has been created with the aim to increase the recognition and diagnosis of dystonia. Molecular biology and genetic studies have identified several genes and biological pathways
openaire   +2 more sources

Dystonia

Current Treatment Options in Neurology, 2000
Therapy for most people with dystonia is symptomatic, directed at lessening the intensity of the dystonic contractions. For a small minority of patients (eg, those with dopa-responsive dystonia, Wilson's disease, or psychogenic dystonia), specific therapy directed at one of the many causes of dystonia is available.
, Bressman, , Greene
openaire   +2 more sources

Dystonia

Current Opinion in Neurology, 1998
Many different disorders have dystonia as the only or primary sign. The list of causes for dystonia increases yearly and now includes three mapped loci for primary torsion dystonia, although other susceptibility genes are suspected. Study of one of these primary torsion dystonia loci (DYT1) has culminated in the cloning of a gene which codes for a ...
openaire   +2 more sources

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