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Molecular and Genetic Basis of Neurological Disease

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ISBN-10: 0750696680

ISBN-13: 9780750696685

Edition: 2nd 1996

Authors: Roger N. Rosenberg, Robert L. Barchi, Stanley B. Prusiner, Salvatore DiMauro

List price: $380.00
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The second edition of this text maintains its reputation as a comprehensive clinical reference for neurologists and geneticists treating patients with genetic neurologic diseases.
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Book details

List price: $380.00
Edition: 2nd
Copyright year: 1996
Publisher: Elsevier - Health Sciences Division
Publication date: 12/23/1996
Binding: Paperback
Pages: 1312
Size: 8.75" wide x 11.75" long x 2.50" tall
Weight: 9.592
Language: English

Molecular Genetics and Neurologic Disease: An Introduction
A Neurologic Gene Map
Finding and Excluding Gene Locations by Linkage Analysis
Gene Targeting
Down Syndrome
Fragile X Syndrome
Molecular Biology of Prion Diseases
Clinical and Neuropathologic Features of Prion Diseases
Inherited Prion Diseases
The Mitochondrial Genome
Mitochondrial Encephalomyelopathies
Mitochondrial Mechanisms of Aging
Peroxisomal Disorders
Refsum Disease
The Mucopolysaccharidoses and the Mucolipidoses
Disorders of Glycoprotein Degradation
Wolman Disease
Ceramidase Deficiency: Farber Lipogranulomatoses
The Niemann-Pick Disease Group
Glucosyceramide Lipidosis: Gaucher Disease
Krabbe Disease (Globoid Cell Leukodystrophy)
Metachromatic Leukodystrophy and Multiple Sulfatase Deficiency
Fabry Disease: Alpha-Galactosidase A Deficiency
Schindler Disease: Deficient Alpha-N-Acetylgalactosamindase Activity
Beta-Galactosidase Deficiency: GM1 Gangliosidosis, Morquio B Disease, and Galactosialidosis
The GM2 Gangliosidoses
Canavan Disease
The Hereditary Ataxias
Huntington Disease
Inherited Disorders of the Basal Ganglia
Alzheimer Disease: Clinical and Genetic Features
Cellular and Molecular Biology of Amyloid and Alzheimer Disease
Cellular and Molecular Biological Aspects of Tau and Alzheimer Disease
Inherited Multiple Sclerosis
Oncogenes and Neuro-Oncology
Tumors of Neuronal Cell Origin
Tumor Suppressor Genes and the Nervous System
The Clinical and Molecular Genetics of Neurofibromitosis I and II
Myotonia Congenita
The Periodic Paralyses
Malignant Hyperthermia and Central Core Disease
Episodic Ataxia and Myokymia
Genetic Epilepsies
Spinal Muscular Atrophy
Inherited ALS
Inherited Demyelinating Neuropathy
Inherited Axonal Neuropathy
Familial Amyloidotic Neuropathy
Congenital Myopathies
Myotonic Dystrophy
Facioscapulohumeral and Limb-Girdle Muscular Dystrophies
Lipid Disorders of Muscle
Xeroderma Pigmentosum
Tuberous Sclerosis
Incontinentia Pigmenti
Disorders of Lipoproteins
Genetics of Apolipoprotein E
The Chemistry of Apolipoprotein E
Cerebrotendinous Xanthomatosis
Disorders of Carbohydrate Metabolism: Glycogen Storage Diseases
Disorders of Galactose Metabolism
Molecular Biology of Alcohol Dependence
Inborn Errors of Amino Acid Metabolism and Transport
Urea Cycle Disorders
Maple Syrup Disease
Glutathione in the Brain: Disorders of Glutathione Metabolism
Lesch-Nyhan Disease and HPRT Deficiency
The Porphyrias
Disorders of Copper Metabolism
Hallervordern-Spatz Disease
Inherited Disorders of Colbalmin and Folate Transport and Metabolism
Disorders of Biotin Metabolism: Treatable Neurologic Syndromes
The Genetics of Bipolar Neurologic Disease
Gene Therapy and Neurologic Disease
Consequences of Mapping and Sequencing the Human Genome for Neurologic Diseases