Dystonia and dystonic syndromes. (2015)
- Record Type:
- Book
- Title:
- Dystonia and dystonic syndromes. (2015)
- Main Title:
- Dystonia and dystonic syndromes
- Further Information:
- Note: Petr Kanovsky, Kailash P. Bhatia, Raymond L. Rosales, editors ; contributors Giovanni Abbruzzese [and twenty five others].
- Editors:
- Kanovsky, Petr
Bhatia, Kailash P
Rosales, Raymond L - Other Names:
- Abbruzzese, G (Giovanni) contributor.
- Contents:
- Contributors; Part I: Pathophysiology and Nosology of Dystonia; 1: Dystonia: The Syndrome, Its Term, Concept and Their Evolution; References; 2: Physiology of Dystonia; 2.1 Introduction; 2.2 Loss of Inhibition; 2.3 Sensory and Sensorimotor Integration Abnormalities; 2.4 Changes of Cortical Plasticity; 2.5 The Role of Basal Ganglia; 2.6 The Role of Cerebellum; Conclusions; References; 3: Genetics of Dystonia; 3.1 Classification of Dystonia; 3.1.1 Isolated Dystonias; 3.1.1.1 TOR1A (DYT1); 3.1.1.2 THAP1 (DYT6); 3.1.1.3 GNAL (DYT25); 3.1.1.4 CIZ1 (DYT23); 3.1.1.5 ANO3 (DYT24) 3.1.1.6 TUBB4 (DYT4)3.1.2 Combined Dystonias; 3.1.2.1 Persistent Combined Dystonias with Parkinsonism; GCH1 (DYT5a), TH (DYT5b), and SPR (no DYT Designation); ATP1A3 (DYT12); PRKRA (DYT16); TAF1 (DYT3); 3.1.2.2 Persistent Combined Dystonias with Myoclonus; SGCE (DYT11); 3.1.2.3 Paroxysmal Combined Dystonias; PNKD (DYT8); SLC2A1 (DYT18/DYT9); PRRT2 (DYT10); 3.2 Inconsistencies of DYT Designation; 3.3 Identification of New Dystonia Genes; 3.4 Genetic Testing: Whom to Test and How?; References; 4: Nosology and Classification of Dystonia; 4.1 Introduction. 4.2 Axis I: Clinical Characteristics of Dystonia4.2.1 Classification by Age at Onset; 4.2.2 Classification by Body Distribution; 4.2.3 Classification According to Temporal Pattern; 4.2.4 Recognition of Associated Features; 4.3 Axis II: Etiology; References; 5: Secondary Dystonia; 5.1 Secondary (Symptomatic) Dystonia; 5.2 Dystonia-Plus Syndromes; 5.2.1Contributors; Part I: Pathophysiology and Nosology of Dystonia; 1: Dystonia: The Syndrome, Its Term, Concept and Their Evolution; References; 2: Physiology of Dystonia; 2.1 Introduction; 2.2 Loss of Inhibition; 2.3 Sensory and Sensorimotor Integration Abnormalities; 2.4 Changes of Cortical Plasticity; 2.5 The Role of Basal Ganglia; 2.6 The Role of Cerebellum; Conclusions; References; 3: Genetics of Dystonia; 3.1 Classification of Dystonia; 3.1.1 Isolated Dystonias; 3.1.1.1 TOR1A (DYT1); 3.1.1.2 THAP1 (DYT6); 3.1.1.3 GNAL (DYT25); 3.1.1.4 CIZ1 (DYT23); 3.1.1.5 ANO3 (DYT24) 3.1.1.6 TUBB4 (DYT4)3.1.2 Combined Dystonias; 3.1.2.1 Persistent Combined Dystonias with Parkinsonism; GCH1 (DYT5a), TH (DYT5b), and SPR (no DYT Designation); ATP1A3 (DYT12); PRKRA (DYT16); TAF1 (DYT3); 3.1.2.2 Persistent Combined Dystonias with Myoclonus; SGCE (DYT11); 3.1.2.3 Paroxysmal Combined Dystonias; PNKD (DYT8); SLC2A1 (DYT18/DYT9); PRRT2 (DYT10); 3.2 Inconsistencies of DYT Designation; 3.3 Identification of New Dystonia Genes; 3.4 Genetic Testing: Whom to Test and How?; References; 4: Nosology and Classification of Dystonia; 4.1 Introduction. 4.2 Axis I: Clinical Characteristics of Dystonia4.2.1 Classification by Age at Onset; 4.2.2 Classification by Body Distribution; 4.2.3 Classification According to Temporal Pattern; 4.2.4 Recognition of Associated Features; 4.3 Axis II: Etiology; References; 5: Secondary Dystonia; 5.1 Secondary (Symptomatic) Dystonia; 5.2 Dystonia-Plus Syndromes; 5.2.1 Dopa-Responsive Dystonia (DRD, DYT-5, DYT-14); 5.2.2 Myoclonus -- Dystonia (DYT-11); 5.3 Heredodegenerative Dystonia; 5.3.1 Heredodegenerative Dystonia in the Mitochondriopathies. 5.3.2 Heredodegenerative Dystonia in the Inherited Metabolic Disorders5.3.3 Heredodegenerative Dystonia Caused by the Storage Diseases; 5.3.4 Heredodegenerative Dystonia Caused by the Nucleotide Repeat Diseases; 5.4 Dystonia as a Feature of Another Neurologic Diseases; References; 6: Dystonia-Parkinsonism Syndromes; 6.1 Introduction; 6.2 Parkinson's Disease and Dystonia; 6.2.1 Parkinson's Disease (PD) Therapy and Dystonia; 6.3 Inherited Diseases of Dystonia and Parkinsonism; 6.3.1 Juvenile-Onset Parkinson's Disease and Dystonia; 6.4 Heredo-degenerative Disorders. 6.4.1 DYT3 or X-Linked Dystonia-Parkinsonism (XDP)6.5 Neurochemical Dystonia-Parkinsonism; 6.5.1 DYT5 or Dopa-Responsive Dystonia (DRD); 6.5.2 DYT12 or Rapid-Onset Dystonia-Parkinsonism (RDP); 6.5.3 DYT16: Early-Onset Dystonia; 6.6 Dystonia-Parkinsonism in Other Characterized Syndromes; 6.6.1 Guadeloupean Parkinsonism; 6.7 Spinocerebellar Ataxia Syndromes; 6.7.1 Spinocerebellar Ataxia 2 (SCA 2); 6.7.2 Spinocerebellar Ataxia 3 (SCA 3); 6.8 Huntington's Disease; References; 7: Dystonia in Multiple System Atrophy, Progressive Supranuclear Palsy, and Corticobasal Degeneration. … (more)
- Publisher Details:
- Heidelberg [Germany] : Springer
- Publication Date:
- 2015
- Copyright Date:
- 2015
- Extent:
- 1 online resource (254 pages), illustrations, photographs
- Subjects:
- 616.8
Nervous system -- Diseases
Dystonia
Dystonia
Nervous system -- Diseases
Medicine
Health & Biological Sciences
Neurology
Dystonic Disorders
Bhatia, Kailash
Electronic books - Languages:
- English
- ISBNs:
- 9783709115169
3709115167
3709115159
9783709115152 - Related ISBNs:
- 9783709115152
3709115159 - Notes:
- Note: Includes bibliographical references at the end of each chapters and index.
Note: Online resource; title from PDF title page (ebrary, viewed April 30, 2015). - Access Rights:
- Legal Deposit; Only available on premises controlled by the deposit library and to one user at any one time; The Legal Deposit Libraries (Non-Print Works) Regulations (UK).
- Access Usage:
- Restricted: Printing from this resource is governed by The Legal Deposit Libraries (Non-Print Works) Regulations (UK) and UK copyright law currently in force.
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD.DS.398880
- Ingest File:
- 02_429.xml