Hyperkinetic Movement Disorders
Handbook of Clinical Neurology Vol. 100 (Series Editors: Aminoff, Boller and Swaab)
Edited by- William Weiner, MD, Professor and Chairman, Department of Neurology, University of Maryland School of Medicine; Director, Maryland Parkinson's Diseases and Movement Disorders Centre, Baltimore, MD, USA
- Eduardo Tolosa, MD, Chief of Neurology Service, Hospital Clinic, University of Barcelona, Spain
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 Huntingtons. 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.
Handbook of Clinical Neurology
Hardbound, 768 Pages
Published: May 2011
Imprint: Elsevier
ISBN: 978-0-444-52014-2
Contents
SECTION 1 - Choreoathetoid Diseases and Syndromes:
1. Huntingtons disease - clinical signs, symptoms, pre-symptomatic diagnosis and diagnosis
2. Huntingtons disease
3. Molecular biology of Huntingtons disease4. Huntingtons disease - neuropathology
5. Huntingtons disease - look-alikes6. Spinocerebellar degenerations
7. Neuroacanthocytosis8. Dentatorubral pallidoluysian atrophy
9. Neurodegeneration with brain iron accumulation10. Movement disorders and mitochondrial disease
11. Acquired hepatocerebral degeneration12. Benign hereditary chorea
13. Senile choreaSECTION 2 - Immune Related Chorea:
14. Sydenhams chorea15. Chorea gravidarum
16. Antiphospholipid sydrome and other lupus related movement disordersSECTION 3 - Vascular Related Chorea:
17. Hemiballismus18. Vascular chorea in adults and children
19. Polycythemia and choreaSECTION 4 - Metabolic Disturbances:
20. Hyperthyroid chorea21. Hyperglycemic non-ketotic states and other metabolic imbalances
SECTION 5 - Chorea in Other Medical Settings:22. Postoperative encephalopathy with choreoathetosis
23. Movement disorders in patients with multiple sclerosis24. Paraneoplastic syndromes causing movement disorders
25. Hyperkinetic movement disorders associated with HIV and other viral infections26. Chorea caused by toxins
27. Drug-induced hyperkinetic movement disorders by non-neuroleptic agentsSECTION 6 - Other Syndromes:
28. Paroxysmal choreodystonic disorders29. Painful legs and moving toes
SECTION 7 - Athetosis:30. Birth-related syndromes of athetosis and kernicterus
SECTION 8 - Myoclonus:31. Myoclonus
32. Startle syndromesSECTION 9 - Essential Tremor:
33. Essential tremor34. Management of essential tremor including medical and surgical approaches
35. Orthostatic tremor - a reviewSECTION 10 - Dystonia:
36. Early-onset primary dystonia37. Adult-onset dystonia
38. Non-primary dystonias39. Dopa responsive dystonia
40. Rapid-onset dystonia-Parkinsonism41. Myoclonus dystonia syndrome
SECTION 11 - Tardive Dyskinesia:42. Typical and atypical neuroleptics
43. Epidemiology of tardive dyskinesia before and during the era of modern antipsychotic drugs44. Unusual focal dyskinesias
SECTION 12 - Tics:45. Stereotypic movement disorders
46. Tourette syndrome and other tic disordersSECTION 13 - Other Syndromes:
47. Restless legs syndrome48. Hemifacial spasm
49. Wilsons disease50. Task-specific tremor
51. Hyperkinetic psychogenic movement disorder

