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Ataxic disorders

Author: Sankara H Subramony; Alexandra Dürr
Publisher: Edinburgh : Elsevier, 2012.
Series: Handbook of clinical neurology, 3rd ser., v. 103.
Edition/Format:   eBook : Document : EnglishView all editions and formats
Summary:
"This volume's primary goal is to provide a comprehensive understanding of recent developments and advancements in the study of ataxic disorders. Beginning with an examination of the cerebellar region, and then progressing to a fresh perspective on the clinical aspects of the various forms of ataxia, this handbook gives clinicians a state-of-the-art reference for the management of the many etiologies and  Read more...
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Genre/Form: Electronic books
Electronic book
Additional Physical Format: Print version:
Ataxic disorders.
Edinburgh ; New York : Elsevier, 2012
(DLC) 2010047033
(OCoLC)680587198
Material Type: Document, Internet resource
Document Type: Internet Resource, Computer File
All Authors / Contributors: Sankara H Subramony; Alexandra Dürr
ISBN: 9780444534941 0444534946
OCLC Number: 776633377
Description: 1 online resource (xviii, 663 pages) : illustrations (some color).
Contents: Basic aspects. The cerebellum --
structure and connections ; Physiology of clinical dysfunction of the cerebellum ; Oculomotor aspects of the hereditary cerebellar ataxias ; Magnetic resonance and nuclear medicine imaging studies in ataxic disease ; Neuropathology of degenerative ataxias ; Approach to ataxic diseases. --
Acquired ataxias. Acquired ataxias, infectious and para-infectious ; Ataxia in patients with brain infarcts and hemorrhages ; Ataxia resulting from posterior fossa tumors of childhood and other mass lesions ; Nutritional cerebellar degeneration, with comments on its relationship to Wernicke disease and alcoholism ; Immune-mediated acquired ataxias ; Toxic agents causing cerebellar ataxias ; Paraneoplastic cerebellar degeneration. --
Degenerative ataxias. Epidemiology and population genetics of degenerative ataxias ; Sporadic adult onset ataxia of unknown aetiology. Degenerative ataxias --
Mitochondrial, autosomal recessive and x-linked. Overview of autosomal recessive ataxias ; Friedrich's ataxia ; Ataxia with vitamin E deficiency and abetalipoproteinemia ; Ataxia-telangiectasia ; Autosomal recessive cerebellar ataxias with oculomotor apraxia ; Other autosomal recessive and childhood ataxias ; Ataxia in mitochondrial disorders ; Fragile X-associated tremor/ataxia syndrome. --
Degenerative ataxias --
autosomal dominant. Overview of autosomal dominant ataxias ; Spinocerebellar ataxia type 1, 2 ; Machado-Joseph disease/spinocerebellar ataxia type 3 ; Spinocerebellar ataxia type 5, 6, 7 ; Clinical and genetic features of spinocerebellar ataxia type 8 ; Spinocerebellar ataxia type 10, 11, 12, 13, 14, 15, 20, 25, 28 ; Other spinocerebellar ataxias ; Dentatorubral-pallidoluysian atrophy ; Episodic ataxias 1 and 2. --
Other issues. Ataxias related to sensory neuropathies ; Frontal lobe ataxia ; Balance and gait problems in the elderly ; Treatment and management issues in ataxic disease.
Series Title: Handbook of clinical neurology, 3rd ser., v. 103.
Responsibility: volume editors, Sankara H. Subramony and Alexandra Dürr.

Abstract:

Provides an understanding of developments and advancements in the study of ataxic disorders. This book gives clinicians a reference for the management of the many etiologies and neurological  Read more...

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