Ataxic Disorders : Handbook of Clinical Neurology (Series Editors: Aminoff, Boller and Swaab).

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 at...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Subramony, Sankara H.
Otros Autores: Dürr, Alexandra
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Burlington : Elsevier Science, 2011.
Colección:Handbook of clinical neurology.
Temas:
Ataxia.
Movement disorders.
Ataxia
Ataxie.
Movement disorders
Acceso en línea:Texto completo

MARC

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245 1 0 |a Ataxic Disorders :  |b Handbook of Clinical Neurology (Series Editors: Aminoff, Boller and Swaab). 
260 |a Burlington :  |b Elsevier Science,  |c 2011. 
300 |a 1 online resource (682 pages). 
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505 0 |a Front Cover; Ataxic Disorders; Copyright; Available Titles; Foreword; Preface; List of Contributors; Contents; Section 1: Basic Aspects; Chapter 1: The cerebellum -- structure and connections; Introduction; External Morphology; Structure of the Cerebellar Cortex; The Cerebellar Nuclei; Cerebellar Corticonuclear-nucleocortical Connections; Olivocerebellar and Cerebello-olivary Interconnections; Afferent Connections of the Cerebellum -- a Synopsis; Efferent Connections of the Cerebellum -- a Synopsis. 
505 8 |a Hypothalamocerebellar and Cerebellohypothalamic Connections: Cerebellar Access to the Visceromotor SystemConcluding Comments; Acknowledgments; Chapter 2: Physiology of clinical dysfunction of the cerebellum; The Cerebellum as a System Controller; Cerebellar Corticonuclear Microcomplexes; Ataxia and Action Tremor Seen as Controller Inadequacy in Command Following and Postural Stabilization; Cerebellar Eye Signs; Impairment of Complex Motor Actions; Impaired Motor Learning; Impairments in Perception And timing; Impairments in Cognition And affect. 
505 8 |a Chapter 3: Oculomotor aspects of the hereditary cerebellar ataxiasSpinocerebellar Ataxia Type 1 (Sca1); Spinocerebellar Ataxia Type 2 (Sca2); Spinocerebellar Ataxia Type 3 (Sca3; Also Known as Machado-joseph Disease Or Mjd); Spinocerebellar Ataxia Type4 (Sca4); Spinocerebellar Ataxia Type 5 (Sca5); Spinocerebellar Ataxia Type 6 (Sca6) (Table3.3); Spinocerebellar Ataxia Type 7 (Sca7) (Table3.3); Spinocerebellar Ataxia Type 8 (Sca8); Spinocerebellar Ataxia Type 10 (Sca10); Spinocerebellar Ataxia Type 11 (Sca11); Spinocerebellar Ataxia Type 12 (Sca12); Spinocerebellar Ataxia Type 13 (Sca13). 
505 8 |a Spinocerebellar Ataxia Type 14 (Sca14)Spinocerebellar Ataxia Type 15 (Sca15); Spinocerebellar Ataxia Type 16 (Sca16); Spinocerebellar Ataxia Type 17 (Sca17); Spinocerebellar Ataxia Type 18 (Sca18); Spinocerebellar Ataxia Type 19 (Sca19); Spinocerebellar Ataxia Type 20 (Sca20); Spinocerebellar Ataxia Type 21 (Sca21); Spinocerebellar Ataxia Type 22 (Sca22); Spinocerebellar Ataxia Type 23 (Sca23); Spinocerebellar Ataxia Type 24 (Sca24); Spinocerebellar Ataxia Type 25 (Sca25); Spinocerebellar Ataxia Type 26 (Sca26); Spinocerebellar Ataxia Type 27 (Sca27); Spinocerebellar Ataxia Type 28 (Sca28). 
505 8 |a Dentatorubral-pallidoluysian Atrophy (Drpla)Episodic Ataxia Type 1 (Ea1); Episodic Ataxia Type 2 (Ea2); Episodic Ataxia Type 3 and Type 4 (Ea-3, Ea-4); Autosomal Recessive Ataxias (Table3.4); Chapter 4: Magnetic resonance and nuclear medicine imaging in ataxias; Introduction; Imaging Techniques for the Evaluation of Ataxias; Acute Ataxias; Autosomal Dominant Inherited ataxias; Recessive Inherited Ataxias; X-Linked Inherited Ataxias; Sporadic Ataxias; Role of Imaging and Perspectives; Chapter 5: Neuropathology of degenerative ataxias; Spinocerebellar Ataxias; Autosomal Recessive Ataxias. 
500 |a Sporadic (idiopathic) Ataxias. 
520 |a 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 neurological manifestations of ataxic disorders. Clinicians will gain a broader understanding of generative ataxias and the genetic disorders associated with them. In addition, new neurophy. 
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650 0 |a Ataxia. 
650 0 |a Movement disorders. 
650 2 |a Ataxia 
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650 7 |a Movement disorders  |2 fast 
700 1 |a Dürr, Alexandra. 
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