The field of movement disorders is one of the key subspecialty areas in clinical neurology, and understanding of the relevant conditions can often be difficult. The scope of this area requires a wide knowledge base, and clinicians might, in the course of a single clinic, need to recall the differential of Huntington's-like disorders, the gene implicated in dopa-responsive dystonia, and compare a case of suspected neuroacanthocytosis with a 'classical' case. Part of the accessible Oxford Textbooks in Clinical Neurology series, this volume covers the basic science and clinical concepts underlying the movement disorders, as well as the diagnosis and treatment of individual hypokinetic and hyperkinetic movement disorders. Specifically written to aid understanding and treatment of a wide range of movement disorders, this textbook includes a useful section covering miscellaneous causes of disordered movement, which are routinely encountered by neurologists. It is also supplemented with illustrative video clips that can be accessed through the concurrent online edition. Although firmly rooted in evidence-based management approaches, the authors included their own top tips and experience on the management of difficult cases where no current guidance exists, engaging the reader and providing a better feel for handling real-world clinical problems. The Oxford Textbook of Movement Disorders is an indispensable reference for neurologists and senior trainees in neurology, as well as any physicians advising people with movement disorders. Table of Contents 1. Overview and historical perspective ; 2. Approach to history taking and examination of the movement disorder patient ; 3. Neuroanatomy for the movement disorder specialist ; 4. Functional aspects of the basal ganglia ; 5. Electrophysiological approaches to the movement disorder patient ; 6. Movement disorders: structural and functional imaging ; 7. Genetic techniques, impact, and diagnostic issues in movement disorders ; 8. Overview of parkinsonism and approach to differential diagnosis ; 9. PD: Premotor features, diagnosis, and early management ; 10. PD: Advanced disease, motor complications, and management ; 11. Non-motor symptom management in Parkinson's disease ; 12. The many faces of parkinsonism - a review of the Parkinson look-alike syndromes ; 13. Multiple system atrophy (MSA) ; 14. Progressive supranuclear palsy and corticobasal degeneration ; 15. Primary dementia syndromes and parkinsonism ; 16. Essential tremor and other tremors ; 17. Dystonia: an overview ; 18. Primary dystonia ; 19. Other dystonias ; 20. Huntington's disease ; 21. Huntington's disease look-alikes ; 22. Non-degenerative choreas ; 23. Wilson's disease ; 24. Tic disorders and stereotypies ; 25. Myoclonus ; 26. Paroxysmal movement disorders ; 27. Hereditary and acquired cerebellar ataxias ; 28. Drug-induced movement disorders ; 29. Systemic disease and movement disorders ; 30. Sleep-related movement disorders ; 31. Psychogenic movement disorders
