About this book
Progress in genetic knowledge is profoundly affecting medical practice, and no clinical specialty has more diseases associated with genetic mutations than neurology. As a more complete picture of the genes which give rise to neurological disease is obtained, trainee and practising neurologists need a guide to basic principles and the more important clinical entities with a genetic component. It is against this background that Neurogenetics: A Guide for Clinicians has been written. The book opens with coverage of genetic testing and counselling. Subsequent chapters discuss genetic factors for all the major neurological diseases, including epilepsy, Alzheimer's disease, Parkinsonism and muscular dystrophies. No book in this field can hope to be fully up to date with the latest research; rather this work provides a framework on which to add new genetic discoveries. Neurogenetics: A Guide for Clinicians provides a synoptic overview for neurologists, medical geneticists and scientists working in the field.
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Table of contents
- Cover
- Neurogenetics: A Guide for Clinicians
- Title
- Copyright
- Contents
- Contributors
- Chapter 1: The human genome project – what it really means and where next
- Chapter 2: Genetic counseling and genetic testing for neurogenetic disorders
- Chapter 3: Alzheimer's disease and related dementias
- Chapter 4: The epilepsies
- Chapter 5: The ataxias
- Chapter 6: Huntington' s disease
- Chapter 7: Parkinsonism
- Chapter 8: Prion diseases
- Chapter 9: Channelopathies
- Chapter 10: Amyotrophic lateral sclerosis and other disorders of the lower motor neuron
- Chapter 11: The muscular dystrophies
- Chapter 12: Charcot–Marie–Tooth diseases
- Chapter 13: Mitochondrial disorders
- Chapter 14: The neurofibromatoses and related disorders
- Chapter 15: The future of neurogenetics
- Index
