Hyperkinetic Movement Disorders 1/e 2012 Handbook of Clinical Neurology 100

Hyperkinetic Movement Disorders 1/e 2012  Handbook of Clinical Neurology 100

William Weiner
Professor and Chairman, Department of Neurology, University of Maryland School  

Key Features

* An authoritative, comprehensive guide to movement disorders
* An invaluable reference for the diagnosis and treatment of hyperkinetic diseases and syndromes
* High-level discussions that are ideal for specialists in movement disorders, practitioners and residents alike

Description

The Handbook of Clinical Neurology Vol 100: Hyperkinetic Movement Disorders discusses hyperkinetic disorders related mainly to basal ganglia dysfunction and pathology. It contains 13 sections and 51 chapters written by authoritative and experienced investigators and clinicians in this extremely broad and diverse group of diseases and syndromes. The first section on choreoathetoid diseases and syndromes includes chapters on Huntington’s disease and Huntington’s disease look-alikes; spinocerebellar degenerations; neuroacanthocytosis; entatorubral-pallidoluysian atrophy; neuroferritinopathy; neurodegeneration with brain iron accumulation; mitochondrial disorders; acquired hepatocerebral degeneration; benign hereditary chorea; and “senile chorea.” The remaining chapters focus on the abnormal involuntary movements associated with each disease or syndrome. These include immune-related chorea, vascular chorea, metabolic disturbances that can induce chorea, chorea in other medical settings (e.g., postpump chorea in children, cancer-related paraneoplastic syndromes), myoclonus, essential tremor, and dystonia, including dystonia plus syndromes. There are also chapters on tardive dyskinesia, unusual clinical syndromes, and tics and stereotyped movements in children. The text is a valuable resource for neurology and psychiatry residents, practicing neurologists and psychiatrists, and specialists in movement disorders.

Readership

Neurologists
Neuroscience research workers