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|a Neurogenetics.
|n Part II /
|c volume editors, Daniel H. Geschwind, Henry L. Paulson, and Christine Klein.
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|a Amsterdam, Netherlands :
|b Elsevier,
|c [2018]
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|c �2018
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|a Includes bibliographical references and index.
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|a 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
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|a Handbook of clinical neurology ;
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