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This textbook provides a comprehensive monography on multiple system atrophy (MSA), a rare and fatal neurodegenerative disorder that presents with autonomic failure and either parkinsonism (MSA-P) or cerebellar ataxia (MSA-C).The underlying neuropathology of MSA is characterized by striatonigral degeneration (SND), olivopontocerebellar atrophy (OPCA) and unique oligodendroglial cytoplasmic alpha-synuclein inclusions. MSA is therefore classified among the alpha-synucleinopathies such as Parkinson`s disease, pure autonomic failure and dementia with Lewy bodies. Over the last decade there have been important advances in early diagnosis, pathogenesis research and clinical trial activity. The monography will cover the entire spectrum ranging from molecular and genetic work to symptomatic and interventional therapies. The book is written for movement disorder clinicians and basic neuroscientists interested in degenerative movement disorders.

Muscular atrophy. --- Neuromuscular diseases. --- Neuromotor disorders --- Neuromuscular disorders --- Amyotrophy --- Atrophy, Muscular --- Medicine. --- Neurosciences. --- Neurology. --- Medicine & Public Health. --- Muscles --- Nervous system --- Neuromuscular diseases --- Diseases --- Neural sciences --- Neurological sciences --- Neuroscience --- Medical sciences --- Medicine --- Neuropsychiatry --- Neurology .

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This book is a guide to the everyday clinical management of disorders of the autonomic nervous system, from identification of the key symptoms of autonomic involvement and comprehensive history taking to choice of treatment. The book will assist the reader in determining the anatomic distribution of the disease, as well as underlying autonomic syndromes, and in transforming the clinical picture into a coherent explanation of the patient’s autonomic problem. In addition, guidelines are provided on selection of the most appropriate autonomic and laboratory tests and formulation of appropriate non-pharmacological and pharmacological management strategies. With cases drawn from clinical experience and a list of available online resources, Bedside Approach to Autonomic Disorders will aid the reader in acquiring the skills that are mandatory in order to put patients on the right clinical track. It will be a valuable guide for trainees and young doctors interested in autonomic disorders from the fields of neurology, internal medicine, cardiology, diabetology, and urology.

Medicine. --- Cardiology. --- Diabetes. --- Neurology. --- Urology. --- Medicine & Public Health. --- Autonomic nervous system --- Diseases. --- Heart --- Internal medicine --- Medicine --- Nervous system --- Neuropsychiatry --- Brittle diabetes --- Diabetes mellitus --- IDDM (Disease) --- Insulin-dependent diabetes --- Ketosis prone diabetes --- Type 1 diabetes --- Carbohydrate intolerance --- Endocrine glands --- Diabetic acidosis --- Glycosylated hemoglobin --- Genitourinary organs --- Diseases --- Neurology .

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Improved diagnostic sophistication is increasingly enabling neurologists to differentiate between Parkinson's disease and other atypical parkinsonism (AP), such as multiple system atrophy, progressive supranuclear palsy, corticobasal degeneration, and dementia with Lewy bodies. The Handbook of Atypical Parkinsonism is a comprehensive survey of all diseases of this category, providing an authoritative guide to the recognition, diagnosis and management of these disorders. Each chapter follows a common structure, commencing with the full basic science of the disorder under consideration, followed by descriptions of the clinical picture and differential diagnosis. Subsequent chapters discuss current and future therapeutic approaches to these difficult conditions. Written and edited by leading practitioners in the field, clinicians in neurology and other specialties will find this book essential to the understanding and diagnosis of this complex group of disorders.

Symptomatic Parkinson's disease. --- Parkinson's disease.