Ataxic Disorders
- 1st Edition, Volume 103 - December 5, 2011
- Latest edition
- Editors: Sankara H. Subramony, Alexandra Dürr
- Language: English
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 th… Read more
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 neurophysiological and imaging techniques are discussed, along with an in-depth examination of the treatment and management protocols of ataxic diseases.
- A volume in the Handbook of Clinical Neurology series, which has an unparalleled reputation as the world's most comprehensive source of information in neurology
- International list of contributors including the leading workers in the field
- Describes the advances which have occurred in clinical neurology and the neurosciences, their impact on the understanding of neurological disorders and on patient care
Neurologists
Neuroscience research workers
Neuroscience research workers
Foreword
Preface
List of contributors
Chapter 1: The cerebellum – structure and connections
Chapter 2: Physiology of clinical dysfunction of the cerebellum
Chapter 3: Oculomotor aspects of the hereditary cerebellar ataxias
Chapter 4: Magnetic resonance and nuclear medicine imaging in ataxias
Chapter 5: Neuropathology of degenerative ataxias
Chapter 6: Approach to ataxic diseases
Chapter 7: Acquired ataxias, infectious and para-infectious
Chapter 8: Ataxia in patients with brain infarcts and hemorrhages
Chapter 9: Ataxia resulting from posterior fossa tumors of childhood and other mass lesions
Chapter 10: Nutritional cerebellar degeneration, with comments on its relationship to Wernicke disease and alcoholism
Chapter 11: Immune-mediated acquired ataxias
Chapter 12: Toxic agents causing cerebellar ataxias
Chapter 13: Paraneoplastic cerebellar degeneration
Chapter 14: Epidemiology and population genetics of degenerative ataxias
Chapter 15: Sporadic adult-onset ataxia of unknown etiology
Chapter 16: Overview of autosomal recessive ataxias
Chapter 17: Friedreich ataxia
Chapter 18: Ataxia with vitamin E deficiency and abetalipoproteinemia
Chapter 19: Ataxia–telangiectasia
Chapter 20: Autosomal recessive cerebellar ataxias with oculomotor apraxia
Chapter 21: Other autosomal recessive and childhood ataxias
Chapter 22: Ataxia in mitochondrial disorders
Chapter 23: Fragile X-associated tremor/ataxia syndrome
Chapter 24: Overview of autosomal dominant ataxias
Chapter 25: Spinocerebellar ataxia type 1
Chapter 26: Spinocerebellar ataxia type 2
Chapter 27: Machado–Joseph disease/spinocerebellar ataxia type 3
Chapter 28: Spinocerebellar ataxia type 5
Chapter 29: Spinocerebellar ataxia type 6
Chapter 30: Spinocerebellar ataxia type 7
Chapter 31: Clinical and genetic features of spinocerebellar ataxia type 8
Chapter 32: Spinocerebellar ataxia type 10
Chapter 33: Spinocerebellar ataxia type 11
Chapter 34: Spinocerebellar ataxia type 12
Chapter 35: Spinocerebellar ataxia 13 and 25
Chapter 36: Spinocerebellar ataxia type 14
Chapter 37: Spinocerebellar ataxia type 15
Chapter 38: Spinocerebellar ataxia type 20
Chapter 39: Spinocerebellar ataxia type 28
Chapter 40: Other spinocerebellar ataxias
Chapter 41: Dentatorubral–pallidoluysian atrophy
Chapter 42: Episodic ataxias 1 and 2
Chapter 43: Ataxias related to sensory neuropathies
Chapter 44: Frontal lobe ataxia
Chapter 45: Balance and gait problems in the elderly
Chapter 46: Treatment and management issues in ataxic diseases
Index
- Edition: 1
- Latest edition
- Volume: 103
- Published: December 5, 2011
- Language: English
SS
Sankara H. Subramony
Affiliations and expertise
Professor of Neurology, McKnight Institute at the University of Florida, Gainesville, USAAD
Alexandra Dürr
Affiliations and expertise
INSERM U289 et Département de Génétique Cytogénétique et Embryologie, Hôpital de la Salpêtrière, Paris, FranceRead Ataxic Disorders on ScienceDirect