The Resource The molecular and genetic basis of neurologic and psychiatric disease, editors, Roger N. Rosenberg ... [et al.]

The molecular and genetic basis of neurologic and psychiatric disease, editors, Roger N. Rosenberg ... [et al.]

Label
The molecular and genetic basis of neurologic and psychiatric disease
Title
The molecular and genetic basis of neurologic and psychiatric disease
Statement of responsibility
editors, Roger N. Rosenberg ... [et al.]
Contributor
Subject
Language
eng
Cataloging source
DNLM/DLC
Dewey number
616.8/0442
Illustrations
  • illustrations
  • plates
Index
index present
LC call number
RC347
LC item number
.M59 2008
Literary form
non fiction
Nature of contents
bibliography
NLM call number
  • 2008 B-090
  • WL 140
NLM item number
M718 2008
http://library.link/vocab/relatedWorkOrContributorName
Rosenberg, Roger N
http://library.link/vocab/subjectName
  • Nervous system
  • Nervous system
  • Molecular neurobiology
  • Neurogenetics
  • Nervous System Diseases
  • Genetic Diseases, Inborn
  • Mental Disorders
Label
The molecular and genetic basis of neurologic and psychiatric disease, editors, Roger N. Rosenberg ... [et al.]
Instantiates
Publication
Bibliography note
Includes bibliographical references and index
Contents
  • 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 -- Down syndrome -- Triplet repeats: genetics, clinical features, and pathogenesis -- Prion diseases -- The mitochondrial genome -- The mitochondrial disorders due to mutations in the mitochondrial genome -- Mitochondrial disorders due to mutations in the nuclear genome -- Mitochondria in neurodegenerative disorders -- Peroxisomal disorders -- Gaucher disease -- The niemann-pick diseases -- The G[m]2 gangliosidoses -- Metachromatic leukodystrophy and multiple sulfatase deficiency: sulfatide lipidosis -- Krabble disease: globoid cell leukodystrophy -- The mucopolysaccharidoses and the mucolipidoses -- Disorders of glycoprotein degradation: sialidosis, fucosidosis, [a]-mannosidosis, ß-mannosidosis, and aspartylglycosaminuria -- ß-galactosidase deficiency: G[m1] gangliosidosis, morquio B disease and galactosialidosis -- Farber disease: acid ceramidase deficiency and farber lipogranulomatosis -- Wolman disease -- Lysosomal membrane disorders: LAMP-2 deficiency -- Fabry disease: [a]-galactosdase a deficiency -- Schindler disease: deficient [a]-N-acetylgalactosaminidase activity -- Alzheimer disease -- Frontotemporal dementias -- Genetics of movement disorders -- The inherited ataxias -- Canavan disease -- The hereditary spastic paraplegias -- Neuro-oncology: the neurofibromatoses -- The genetic epilepsies -- Multiple sclerosis --
  • 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
Dimensions
29 cm.
Edition
4th ed.
Extent
xxi, 882 p., 8 p. of plates
Isbn
9780781769563
Lccn
2007020775
Other physical details
ill. (some col.)
System control number
  • (CaMWU)u1965799-01umb_inst
  • 1807337
  • (OCoLC)134990981
Label
The molecular and genetic basis of neurologic and psychiatric disease, editors, Roger N. Rosenberg ... [et al.]
Publication
Bibliography note
Includes bibliographical references and index
Contents
  • 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 -- Down syndrome -- Triplet repeats: genetics, clinical features, and pathogenesis -- Prion diseases -- The mitochondrial genome -- The mitochondrial disorders due to mutations in the mitochondrial genome -- Mitochondrial disorders due to mutations in the nuclear genome -- Mitochondria in neurodegenerative disorders -- Peroxisomal disorders -- Gaucher disease -- The niemann-pick diseases -- The G[m]2 gangliosidoses -- Metachromatic leukodystrophy and multiple sulfatase deficiency: sulfatide lipidosis -- Krabble disease: globoid cell leukodystrophy -- The mucopolysaccharidoses and the mucolipidoses -- Disorders of glycoprotein degradation: sialidosis, fucosidosis, [a]-mannosidosis, ß-mannosidosis, and aspartylglycosaminuria -- ß-galactosidase deficiency: G[m1] gangliosidosis, morquio B disease and galactosialidosis -- Farber disease: acid ceramidase deficiency and farber lipogranulomatosis -- Wolman disease -- Lysosomal membrane disorders: LAMP-2 deficiency -- Fabry disease: [a]-galactosdase a deficiency -- Schindler disease: deficient [a]-N-acetylgalactosaminidase activity -- Alzheimer disease -- Frontotemporal dementias -- Genetics of movement disorders -- The inherited ataxias -- Canavan disease -- The hereditary spastic paraplegias -- Neuro-oncology: the neurofibromatoses -- The genetic epilepsies -- Multiple sclerosis --
  • 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
Dimensions
29 cm.
Edition
4th ed.
Extent
xxi, 882 p., 8 p. of plates
Isbn
9780781769563
Lccn
2007020775
Other physical details
ill. (some col.)
System control number
  • (CaMWU)u1965799-01umb_inst
  • 1807337
  • (OCoLC)134990981

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