The molecular and genetic basis of neurologic and psychiatric disease
著者
書誌事項
The molecular and genetic basis of neurologic and psychiatric disease
Lippincott Williams & Wilkins, c2008
4th ed
大学図書館所蔵 全15件
  青森
  岩手
  宮城
  秋田
  山形
  福島
  茨城
  栃木
  群馬
  埼玉
  千葉
  東京
  神奈川
  新潟
  富山
  石川
  福井
  山梨
  長野
  岐阜
  静岡
  愛知
  三重
  滋賀
  京都
  大阪
  兵庫
  奈良
  和歌山
  鳥取
  島根
  岡山
  広島
  山口
  徳島
  香川
  愛媛
  高知
  福岡
  佐賀
  長崎
  熊本
  大分
  宮崎
  鹿児島
  沖縄
  韓国
  中国
  タイ
  イギリス
  ドイツ
  スイス
  フランス
  ベルギー
  オランダ
  スウェーデン
  ノルウェー
  アメリカ
注記
Includes bibliographical references and index
HTTP:URL=http://www.loc.gov/catdir/enhancements/fy0738/2007020775-d.html Information=Publisher description
内容説明・目次
内容説明
Completely updated for its Fourth Edition, this book is the most comprehensive, current review of the molecular and genetic basis of neurologic and psychiatric diseases. More than 120 leading experts provide a fresh, new assessment of recent molecular, genetic, and genomic advances, offer new insights into disease pathogenesis, describe the newest available therapies, and explore promising areas of therapeutic development. This edition features an updated section on psychiatric disease and expanded, updated chapters on human genomics, gene therapy, and ethical issues. Six new chapters cover congenital myasthenic syndromes, hereditary spastic paraplegia, ion channel disorders, the phakomatoses, beta-galactosidase deficiency, and prion diseases. A Neurologic Gene Map describes the chromosome locus of all the genetic diseases and their gene product where known. The fully searchable online text will be available on a companion Website. (www.rosenbergneuroandpsychdisease.com)
目次
GENERAL CONCEPTS OF MECHANISMS OF DISEASE: Repeat Expansion Disorders: General Concepts and Mechanisms of Disease / Mendelian, Nonmendelian, 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 / Human Genomics and Disease / Gene Therapy for Central Nervous System Disorders / Emerging Ethical Issues in Neurology, Psychiatry, and the Neurosciences / Genotype-Phenotype Correlations NEUROLOGIC DISEASES: Down Syndrome / Triplet Repeat Diseases: Genetics, Clinical Features, and Pathogenesis / Prion Diseases Mitochondrial Disorders: The Mitochondrial Genome / Mitochondrial Disorders Due to Mutations in the Mitochondrial Genome / Mitochondrial Disorders Due to Mutations in the Nuclear Genome / Mitochondria in Neurodegenerative Disorders Peroxisomal Disorders: Perioxisomal Disorders Lysosomal Disorders: Gaucher Disease / The Niemann-Pick Diseases / The Gm2-Gangliosidoses / Metachromatic Leukodystrophy and Multiple Sulfatase Deficiency: Sulfatide Lipidosis / Krabbe Disease: Globoid Cell Leukodystrophy / The Mucopolysaccharidoses and the Mucolipidoses / Disorders of Glycoprotein Degradation: Sialidosis, Fucosidosis, Alpha-Mannosidosis, Beta- / Beta-Galactosidase Deficiency: GM1 Gangliosidosis, Morquio B Disease, and Galactosialidosis / Farber Disease: Acid Ceramidase Deficiency, Farber Lipogranulomatosis / Wolman Disease / Lysosomal Membrane Disorders: LAMP-2 Deficiency / Fabry Disease: Alpha Galactosidase A Deficiency / Schindler Disease: Deficient Alpha-N-Acetylgalacosaminidase Activity Degenerative Disorders: Alzheimer's Disease / Frontotemporal Dementias / Genetics of Movement Disorders / The Inherited Ataxias / Canavan Disease / Hereditary Spastic Paraplegia Neuro-Oncology: Neuro-Oncology: The Neurofibromatoses Epilepsy: The Genetic Epilepsies Demyelinating Disease: Demyelinating Diseases Neuropathies and Neuronopathies: Peripheral Neuropathies / The Molecular and Genetic Basis of Spinal Muscular Atrophies Congenital Myasthenic Syndromes: Congenital Myasthenic Syndromes Myopathies: Dystrophinopathies / Limb-Girdle Muscular Dystrophies / The Congenital Myopathies / The Distal Myopathies / Hereditary Inclusion-Body Myopathies / The Myotonic Dystrophies / Facioscapulohumeral Dystrophy / Ion Channel Disorders Dermatologic and Brain Disorders: The Phakomatoses / Lipoprotein Disorders / Apolipoprotein E: Structure and Function in Lipid Metabolism and Neurobiology / Cerebrotendinous Xanthomatosis Metabolic Disorders: 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 and Biochemical Perspectives / Congenital Disorders of N-linked Glycosylation / Disorders of Glutathione Metabolism Purines: Purines Porphyrias: The Porphyrias Metal Metabolism: Friedreich Ataxia / Disorders of Copper Metabolism: Wilson Disease and Menkes Disease Vitamins: Genetic and Dietary Influences on Life Span / Vitamins: Cobalamin and Folate / Disorders of Biotin Metabolism: Treatable Neurologic Syndromes PSYCHIATRIC DISEASE: Psychiatric Diseases: Challenges in Psychiatric Genetics / Depression / Bipolar Disorder / Schizophrenia / Obsessive-Compulsive Disorder and Tourette's Syndrome / Genetic Bases of Addictive Behaviors / Autism A NEUROLOGIC GENE MAP: A Neurologic Gene Map
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