Neurogenetics: Neurogenetics
In this book, the authors use their extensive experience in the field of neurogenetics to provide readers with a practical approach for dealing with these conditions. The 31 chapters of this book cover a broad range of neurogenetic disorders, highlighting key issues with regards to the clinical assessment, diagnosis and management.
Read More ↓Title Statements
- Full title :Neurogenetics : Neurogenetics.
Summary
In this book, the authors use their extensive experience in the field of neurogenetics to provide readers with a practical approach for dealing with these conditions. The 31 chapters of this book cover a broad range of neurogenetic disorders, highlighting key issues with regards to the clinical assessment, diagnosis and management.
Read More ↓Edition Statements
- Publication Date:©2014
Publication Statements
- Publisher(s):Oxford University Press, Incorporated
- Place of Publication:Cary
- Language:eng
- Publication Date:©2014
The Physical Object
- Description:1 online resource (209 pages)
Edition Identifiers
- ISBN:9780199383900, 0199383901
- oclc:on1119529084
- LC Classification:RC346.4
- Dewey Decimal:616.8/0442
Table of Contents
Cover -- Neurogenetics -- Copyright -- Contents -- List of Figures -- List of Tables -- Preface -- Acknowledgments -- Glossary of Abbreviations -- 1 Early-Onset Dystonia -- 2 Dopa-Responsive Dystonia -- 3 Myoclonus-Dystonia -- 4 Paroxysmal Dyskinesia -- 5 Huntington Disease -- 6 Dominant Parkinson Disease -- 7 Recessive Parkinson Disease -- 8 Gaucher Disease and Parkinson Disease -- 9 Spinocerebellar Ataxia Type 2 -- 10 Spinocerebellar Ataxia Type 17 -- 11 Sialidosis -- 12 Friedreich Ataxia -- 13 Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) Syndrome -- 14 Myoclonus Epilepsy and Ragged Red Fiber (MERRF) -- 15 POLG-Related Mitochondrial Disease -- 16 Mitochondrial Neurogastrointestinal Encephalopathy (MNGIE) Syndrome -- 17 Leber Hereditary Optic Neuropathy -- 18 Charcot-Marie-Tooth Disease Type 1 -- 19 Hereditary Neuropathy with Liability to Pressure Palsies -- 20 Neurofibromatosis Type 1 -- 21 The Myotonic Dystrophies -- 22 The Dystrophinopathies -- 23 Facioscapulohumeral Dystrophy -- 24 Inclusion Body Myopathy with Paget Disease of Bone and/or Frontotemporal Dementia -- 25 Hereditary Spastic Paraplegia -- 26 Inherited Prion Diseases -- 27 Fron…
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