Neurogenetics. Part II / volume editors, Daniel H. Geschwind, Henry L. Paulson, and Christine Klein.

Format:

Book

Contributor:

Geschwind, Daniel H., editor.

Paulson, Henry L., editor.

Klein, Christine, 1969- editor.

Series:

Handbook of clinical neurology ; v. 148.

Handbook of clinical neurology ; volume 148

Language:

English

Subjects (All):

Neurogenetics.

Nervous system--Diseases--Genetic aspects.

Nervous system.

Nervous System Diseases--genetics.

Genetic Diseases, Inborn.

Neurodevelopmental Disorders--genetics.

Genetics, Medical--methods.

Genetic Testing.

Medical Subjects:

Nervous System Diseases--genetics.

Genetic Diseases, Inborn.

Neurodevelopmental Disorders--genetics.

Genetics, Medical--methods.

Genetic Testing.

Genre:

Electronic books.

Physical Description:

1 online resource (xvii, 417, I-23 pages) : illustrations (some color).

Distribution:

©2018.

Place of Publication:

Amsterdam, Netherlands : Elsevier, [2018]

System Details:

text file

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

Notes:

Includes bibliographical references and index.

Description based on online resource; title from electronic title page (ScienceDirect, viewed February 26, 2018).

Other Format:

Print version: Neurogenetics.

ISBN:

9780444640772

0444640770

OCLC:

1019738513

Access Restriction:

Restricted for use by site license.