Marsden's Book of Movement Disorders

333,53 €
Disponible
ISBN
9780192619112
Edición
1st
Autores
C. David Marsden
Editorial
Oxford University Press
Fecha Publicacion
1 may. 2011
Características
N/D
Estimated publication May 2011 This book represents the final work of the late Professor C. David Marsden, who was the most influential figure in the field of movement disorders, in terms of his contributions to both research and clinical practice, in the modern era. It was conceived and written by David Marsden and his colleague at the Institute of Neurology, Prof. Ivan Donaldson. It was their intention that this would be the most comprehensive book on movement disorders and also that it would serve as the 'clinical Bible' for the management of these conditions. It provides a masterly survey of the entire topic, which has been made possible only by vast laboratory and bedside experience. Marsden's Book of Movement Disorders covers the full breadth of movement disorders, from the underlying anatomy and understanding of basal ganglia function to the diagnosis and management of specific movement disorders, including the more common conditions such as Parkinson's Disease through to rare, and very rare conditions such as Neimann-Pick disease. Chapters follow a structured format with historical overviews, definitions, clinical features, differential diagnosis, investigations and treatment covered in a structured way. It is extensively illustrated with many original photographs and diagrams of historical significance. Among these illustrations are still images of some original film clips of some of Dr. Marsden's patients published here for the first time. Comprehensively referenced and updated by experts from the Institute of Neurology at Queen Square, this book is a valuable reference for, not just movement disorder specialists and researchers, but also for clinicians who care for patients with movement disorders. Readership: This book is a valuable reference for, not just movement disorder specialists and researchers, but also for clinicians who care for patients with movement disorders. TABLE OF CONTENTS Section 1 - Introduction 1: Anatomy 2: Functions of the basal ganglia Section 2 - The clinical approach to movement disorders 3: Clinical assessment 4: Investigation Section 3 - Akinetic-rigid syndromes Section 3a - Idiopathic/primary syndromes 5: Parkinson's disease 6: Multiple system atrophy 7: Progressive supranuclear palsy (or Steele-Richardson-Olszewski disease) 8: Corticobasal degeneration 9: Parkinsonian-dementia syndromes Section 3b - Symptomatic Parkinsonian syndromes inherited 10: Wilson's disease 11: Pantothenate kinase-associated neurodegeneration (PKAN), previously also known as Hallervorden-Spatz disease Section 3c - Symptomatic Parkinsonian syndromes aquired 12: Postencephalic parkinsonism 13: Drug-induced parkinsonism and the neuroleptic malignant syndrome 14: Basal ganglia calcification 15: Other acquired symptomatic parkinsonian syndromes Section 4 - Tremor 16: Physiological and exaggerated or enhanced physiological tremor 17: Classical essential tremor 18: Isolated site-specific or task-specific tremors 19: Symptomatic tremors Section 5 - Chorea 20: Huntington's disease 21: Other idiopathic choreic syndromes 22: Sydenham's chorea 23: Spontaneous oro-facial chorea and tardive dyskinesia 24: Other symptomatic (secondary) choreic syndromes 25: Ballism Section 6 - Tics 26: Simple tics 27: Gilles de la Tourette's syndrome 28: Symptomatic (secondary) tic syndromes Section 7 - Myoclonus 29: Focal myoclonus 30: Epileptic myoclonus 31: Brainstem myoclonus and startle syndromes 32: Specific myoclonic syndromes 33: Other, specific causes of symptomatic generalised myoclonus 34: Essential myoclonus Section 8 - Primary idiopathic dystonic syndrome Section 8a - Primary idiopathic dystonic syndrome 35: Generalised primary dystonia 36: Other primary dystonias (dystonia-plus syndromes) 37: Idiopathic (primary) cranial dystonias 38: Spasmodic torticollis 39: Writer's and craft cramps Section 8b - Secondary (symptomatic) dystonic syndromes 40: Lesch-Nyhan syndrome 41: Other inherited secondary (symptomatic) dystonias 42: Cerebral palsy 43: Other acquired secondary (symptomatic) dystonic syndromes Section 9 - Syndromes ofcontinuous muscle fibre activity 44: Stiff man syndromes 45: Neuromyotonic syndromes Section 10 - Restlessness 46: Akathisia 47: Restless legs syndrome 48: Painful legs and moving toes Section 11 - Episodic movement disorders 49: Paroxysmal choreic, athetotic or dystonic attacks 50: Tonic attacks 51: Intermittent ataxias 52: Miscellaneous movement disorders
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