The Molecular and Genetic Basis of Neurologic and Psychiatric Disease is the most comprehensive and up-to-date review of the molecular and genetic basis of neurologic and psychiatric diseases.
Features
- Experts provide a fresh, new assessment of recent molecular, genetic, and genomic advances
- Offers new insights into disease pathogenesis
- Describes the newest available therapies
- Explores promising areas of therapeutic development
- A Neurologic Gene Map describes the chromosome locus of all the genetic diseases and their gene product where known
The Molecular and Genetic Basis of Neurologic and Psychiatric Disease includes a companion website that features the fully searchable text online so the reader will have a fast, flexible multimedia library at their service.
Contents
General Concepts and Mechanisms of Disease
- Repeat Expansion Disorders: General Concepts and Mechanisms of Disease
- Mendelian, Nonmendelian, and Multigenic Inheritance and Complex Traits
- Selected Genetically Engineered Models Relevant to Human Neurodegenerative Disease
- Gene Mapping to Gene Targeting: Application of Mouse Genetics to Human Disease
- Genomics and the Human Genome Project
- Gene Therapy for Central Nervous System Disorders
- Emerging Ethical Issues in Neurology, Psychiatry, and the Neurosciences
- Genotype-Phenotype Correlations
Neurologic Diseases
- Down Syndrome
- Triplet Repeats: Genetics, Clinical Features, and Pathogenesis
- Prion Diseases
Part A: A Mitochondrial Disorders
- The Mitochondrial Genome
- Mitochondrial Disorders Due to Mutations in the Mitochondrial Genome
- Mitochondrial Disorders Due to Mutations in the Nuclear Genome
- Mitochondrial in Neurodegenerative Disorders
Part B: Peroxisomal Disorders
- Peroxisomal Disorders
Part C: Lysosomal Disorders
- Gaucher Disease
- The Niemann-Pick Diseases
- The GM2 Gangliosidoses
- Metachromatic Leukodystrophy and Multiple Sulfatase Deficiency: Sulfatide Lipidosis
....and chapters 21-29
Part D: Degenerative Disorders
- Alzheimer Disease
- Frontotemporal Dementias
- Genetics of Movement Disorders
- The Inherited Ataxias
- Canavan Disease
- The Hereditary Spastic Paraplegias
Parts E-I
Chapters 36-41
Part J: Myopathies
- Dystrophinopathies
- Limb-Girdle Muscular Dystrophies
- The Congenital Myopathies
...and chapters 45-49
Part K: Dermatologic and Brain Disorders
- The Phakomatoses
- Lipoprotein Disorders
- Apolipoprotein E: Structure and Function in Lipid Metabolism and Neurobiology
- Cerebrotendinous Xanthomatosis
Part L: Metabolic Disorders
- Disorders of Lipid Metabolism
- Glycogen Storage Diseases
- Disorders of Galactose Metabolism
- Inborn Errors of Amino Acid Metabolism
...and chapters 58-62
Parts M-O
Chapters 63-66
Part P: Vitamins
- Genetic and Dietary Influences on Life Span
- Vitamins: Cobalamin and Folate
- Disorders of Biotin Metabolism: Treatable Neurologic Syndromes
Psychiatric Disease
Chapters 70-76
A Neurologic Gene Map
- A Neurologic Gene Map
Index