Results 251 to 260 of about 59,501 (281)
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Australian & New Zealand Journal of Psychiatry, 1989
Unlike tardive dyskinesia (TD) which is much better known by clinicians, tardivedystonia is a more recently recognised complication of neuroleptic use. It refers to chronic dystonia related to the use of neuroleptic drugs and may be an even more disabling condition than TD. This article reviews its epidemiology, clinical features and treatment aspects,
H F, Chiu, S, Lee
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Unlike tardive dyskinesia (TD) which is much better known by clinicians, tardivedystonia is a more recently recognised complication of neuroleptic use. It refers to chronic dystonia related to the use of neuroleptic drugs and may be an even more disabling condition than TD. This article reviews its epidemiology, clinical features and treatment aspects,
H F, Chiu, S, Lee
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Parkinsonism & Related Disorders, 2018
Dystonia is a rare disorder that has undergone extensive scientific investigation leading to a transformation of understanding over the past century.This manuscript was prepared through a review of relevant literature for each topic.Historically dystonia was considered the manifestation of psychiatric disorders. Subsequently, investigations have firmly
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Dystonia is a rare disorder that has undergone extensive scientific investigation leading to a transformation of understanding over the past century.This manuscript was prepared through a review of relevant literature for each topic.Historically dystonia was considered the manifestation of psychiatric disorders. Subsequently, investigations have firmly
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Movement Disorders, 2011
AbstractThe last 25 years have seen remarkable advances in our understanding of the genetic etiologies of dystonia, new approaches into dissecting underlying pathophysiology, and independent progress in identifying effective treatments. In this review we highlight some of these advances, especially the genetic findings that have taken us from ...
Laurie J, Ozelius +2 more
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AbstractThe last 25 years have seen remarkable advances in our understanding of the genetic etiologies of dystonia, new approaches into dissecting underlying pathophysiology, and independent progress in identifying effective treatments. In this review we highlight some of these advances, especially the genetic findings that have taken us from ...
Laurie J, Ozelius +2 more
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Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology, 2007
Oromandibular dystonia (OMD) is a rare neuromuscular disorder characterized by involuntary repetitive muscular contraction affecting different parts of the oromandibular region. Its various physical manifestations can be extremely debilitating and socially disabling to affected patients. To date, there is no commonly accepted set of diagnostic criteria
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Oromandibular dystonia (OMD) is a rare neuromuscular disorder characterized by involuntary repetitive muscular contraction affecting different parts of the oromandibular region. Its various physical manifestations can be extremely debilitating and socially disabling to affected patients. To date, there is no commonly accepted set of diagnostic criteria
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Parkinsonism & Related Disorders, 2007
Dystonia varies in severity from simple focal dystonia, such as writer's cramp to life-threatening status dystonicus. Even though the pathophysiology is still elusive, symptomatic treatments may provide marked relief. Botulinum toxin is considered the treatment of choice for most focal and segmental dystonias.
Octavian R, Adam, Joseph, Jankovic
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Dystonia varies in severity from simple focal dystonia, such as writer's cramp to life-threatening status dystonicus. Even though the pathophysiology is still elusive, symptomatic treatments may provide marked relief. Botulinum toxin is considered the treatment of choice for most focal and segmental dystonias.
Octavian R, Adam, Joseph, Jankovic
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Seminars in Neurology, 2007
During the last decade, we have witnessed significant advances in the study of inherited dystonias. This article will review some of those discoveries and summarize their significance for the practicing neurologist. A clinical classification of dystonia based on features that can be determined by the clinician is proposed, aiming to facilitate the ...
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During the last decade, we have witnessed significant advances in the study of inherited dystonias. This article will review some of those discoveries and summarize their significance for the practicing neurologist. A clinical classification of dystonia based on features that can be determined by the clinician is proposed, aiming to facilitate the ...
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Journal of the Neurological Sciences, 2017
In most cases the cause for dystonia is unknown. In a small number of patients, trauma precedes the onset of the dystonia. Significant head trauma is a well-recognized precipitating factor in dystonia. However, it has become increasingly recognized that peripheral trauma can also result in dystonia.
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In most cases the cause for dystonia is unknown. In a small number of patients, trauma precedes the onset of the dystonia. Significant head trauma is a well-recognized precipitating factor in dystonia. However, it has become increasingly recognized that peripheral trauma can also result in dystonia.
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2011
Dystonias can be classified as primary or secondary, as dystonia-plus syndromes, and as heredodegenerative dystonias. Their prevalence is difficult to determine. In our experience 80-90% of all dystonias are primary. About 20-30% of those have a genetic background; 10-20% are secondary, with tardive dystonia and dystonia in cerebral palsy being the ...
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Dystonias can be classified as primary or secondary, as dystonia-plus syndromes, and as heredodegenerative dystonias. Their prevalence is difficult to determine. In our experience 80-90% of all dystonias are primary. About 20-30% of those have a genetic background; 10-20% are secondary, with tardive dystonia and dystonia in cerebral palsy being the ...
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The epidemiology of dystonia: the Hannover epidemiology study
Journal of Neurology, 2022Joachim Krauss +2 more
exaly