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The molecular and genetic basis of neurologic and psychiatric disease
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The molecular and genetic basis of neurologic and psychiatric disease

Publication Data

Contents

Peripheral neuropathies
The molecular and genetic basis of spinal muscular atrophies
Congenital myasthenic syndromes
Dystrophinopathies
Limb-girdle muscular dystrophies
The congenital myopathies
The distal myopathies
Hereditary inclusion-body myopathies
The myotonic dystrophies
Facioscapulohumeral dystrophy
Ion channel disorders
The phakomatoses
Lipoprotein disorders
Apolipoprotein E: structure and function in lipid metabolism and neurobiology
Cerebrotendinous xanthomatosis
Disorders of lipid metabolism
Glycogen storage diseases
Disorders of galactose metabolism
Inborn errors of amino acid metabolism
Disorders of the urea cycle
Disorders of glucose transport
Maple syrup urine disease: clinical biochemical considerations
Congenital disorders of N-linked glycosylation
Disorders of glutathione metabolism
Disorders of purine metabolism
The porphyrias
Friedreich ataxia
Disorders of copper metabolism: Wilson disease and Menkes disease
Genetic and dietary influences on life span
Vitamins: cobalamin and folate
Disorders of biotin metabolism: treatable neurologic syndromes
Psychiatric diseases: challenges in psychiatric genetics
Depression
Bipolar disorder
Schizophrenia
Obessive-compulsive disorder and tourette syndrome
Genetic bases of addictive behaviors
Autism
A neurologic gene map.

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The molecular and genetic basis of neurologic and psychiatric disease. ISBN 9780781769563. Published by Lippincott Williams & Wilkins in 2008. Publication and catalogue information, links to buy online and reader comments.

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