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.
* 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
Le informazioni nella sezione "Riassunto" possono far riferimento a edizioni diverse di questo titolo.
This volume provides valuable insights into hyperkinetic disorders related mainly to basal ganglia and pathology. It is divided into comprehensive chapters that encompass a broad and diverse group of diseases and syndromes that are characterized by abnormal, involuntary movements.
Clinicians will find a plethora of information, including extensive discussions of choreoathtoid diseases like Huntington s. Additional chapters focus on topics including, but not limited to, spinocerebellar degenerations, neurodegeneration with brain iron accumulation, immune-related chorea, cancer-related paraneoplastic syndromes, myoclonus, essential tremor, dystonia, tartive dyskinesia, and tics and stereotyped movements in children.
Advancements in treatment protocols for these syndromes and diseases are also presented. Each chapter serves as an authoritative reference on its topic, making this handbook ideally suited for neurology and psychiatry residents, practicing neurologists and psychiatrists, and specialists in movement disorders.
Le informazioni nella sezione "Su questo libro" possono far riferimento a edizioni diverse di questo titolo.
Da: Chiron Media, Wallingford, Regno Unito
Paperback. Condizione: New. Codice articolo 6666-ELS-9780444520142
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Da: Majestic Books, Hounslow, Regno Unito
Condizione: New. pp. 768. Codice articolo 4384567
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Da: Brook Bookstore On Demand, Napoli, NA, Italia
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Da: Books Puddle, New York, NY, U.S.A.
Condizione: New. pp. 768 1st Edition. Codice articolo 263496168
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Da: Revaluation Books, Exeter, Regno Unito
Hardcover. Condizione: Brand New. 1st edition. 768 pages. 11.25x8.75x1.75 inches. In Stock. Codice articolo __0444520147
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Da: Biblios, Frankfurt am main, HESSE, Germania
Condizione: New. pp. 768. Codice articolo 183496162
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