Neurogenetics. Part II /
Call Number: | Libro Electrónico |
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Other Authors: | , , |
Format: | Electronic eBook |
Language: | Inglés |
Published: |
Amsterdam, Netherlands :
Elsevier,
[2018]
|
Series: | Handbook of clinical neurology ;
v. 148. |
Subjects: | |
Online Access: | Texto completo |
Table of Contents:
- Section V. Dementias. The genetic landscape of Alzheimer disease
- Frontotemporal dementia
- The genetics of dementia with Lewy bodies
- Prion disease
- Section VI. Paroxysmal disorders. Genetics of epilepsy
- Genetics of migraine
- Periodic paralysis
- Episodic ataxias
- Disorders of sleep and circadian rhythms
- Section VII. Neuromuscular disorders. Facioscapulohumeral muscular dystrophy
- The genetics of congenital myopathies
- Genetic basis and phenotypic features of congenital myasthenic syndromes
- Spinal muscular atrophy
- Emerging understanding of the genotype: Phenotype relationship in amyotrophic lateral sclerosis
- Spinal and bulbar muscular atrophy
- Hereditary spastic paraplegia
- Neuropathy
- Section VIII. Diseases of white matter and demyelination. The spectrum of adult-onset heritable white matter disorders
- Alexander disease
- Neurogenetics of Pelizaeus-Merzbacher disease
- Multiple sclerosis
- Section IX. Cerebrovascular diseases. CADASIL
- Section X. Major adult psychiatric disorders. Neuroepigenetics and addiction
- Genetic susceptibility in obsessive-compulsive disorder
- Section XI. Cancer and phakomatoses. Brain cancer genomics and epigenomics
- Neurofibromatosis type 1
- Tuberous sclerosis complex
- Von Hippel-Lindau disease and Sturge-Weber syndrome